Patent Application
20140121163
Throughout this application various publications are referred to in parentheses. Full citations for these references may be found at the end of the specification. The disclosures of these publications are hereby incorporated by reference in their entirety into the subject application to more fully describe the art to which the subject invention pertains.
Inflammation and apoptosis play crucial roles in the evolution of cerebral infarct following ischemic insult. Following necrotic cell death in the core of the cerebral infarct, cell death in the relatively hypoperfused penumbra occurs over time through inflammatory and apoptotic mechanisms. The inflammatory process involves NF-κB mediated release of cytokines, such as TNF-α, which cause cell injury (Dirnagl et al. 1999). Apoptosis involves release of pro-apoptotic molecules such as bax, and activation of the caspases leading to DNA fragmentation and cell death. The cell-damaging mechanisms that are activated by ischemia are countered by cell-survival mechanisms including upregulation of anti-apoptotic molecules such as bcl-2 (Antonsson 2004). The peroxisome-proliferator activated receptor-γ (PPAR-γ) is a ligand-inducible transcription factor that has been shown to counteract inflammation by downregulating cytokine release (Ricote and Glass 2007). Therapeutic suppression of inflammation and apoptosis could rescue the penumbra after ischemic stroke.
Sepsis is one of the most prevalent diseases and accounts for 20% of all admissions to intensive care units (ICUs) (Angus, et al., 2001). Evidence indicates that in the U.S. alone, more than 750,000 people develop sepsis each year with an overall mortality rate of 28.6% (Angus, et al., 2001). Despite advances in the management of septic patients, a large number of such patients die of the ensuing septic shock and multiple organ failure (Ferrer, et al., 2008; Strehlow, et al., 2006; Martin, et al., 2003; Guidet, et al., 2005). An analysis of hospital records indicates that the total number of patients who have died of sepsis is actually increasing (Martin, et al., 2003). As the American population ages, the incidence of sepsis is projected to increase since the incidence and mortality rate of sepsis rise steadily with aging (Angus, et al., 2001; Martin, et al., 2003). Thus, there is an urgent unmet medical need for an effective novel therapy for patients with sepsis.
Milk fat globule-EGF factor VIII (MFG-E8), also known as lactadherin, is a 66-kDa glycoprotein originally discovered in mouse milk and mammary epithelium (Stubbs et al, 1990). It is an important milk mucin-associated defense component that inhibits enterie pathogen binding and infectivity (Yolken, et al., 1992). MFG-E8 was subsequently found to be widely distributed in various tissues in mice and other mammalian species including humans (Aziz et al. 2009; Hanayama et al. 2004; Larocca et al. 1991). In the brain, MFG-E8 is expressed in astrocytes (Boddaert et al. 2007) and microglia (Fuller and Van Eldik 2008). MFG-E8 contains two N-terminals epidermal growth factor (EGF)-like repeats, and two C-terminal discoidin/F5/8C domains. MFG-E8 binds αvβ3/5 integrin heterodimers through an arginine-glycine-aspartic acid (RGD) motif contained in the second EGF domain (Anderson et al. 1997).
Recent studies have shown that MFG-E8 can also be secreted by activated macrophages and immature dendritic cells and has been linked to the opsonization of apoptotic cells (Hanayama, et al., 2002; Hanayama, et al., 2004; Miyasaka, et al., 2004; Thery, et al., 1999; Oshima, et al., 2002). The second F5/8C domain of MFG-E8 has high affinity for anionic membrane phospholipids such as phosphatidylserine that become externalized during apoptosis (Anderson et al, 1997; Shao et al. 2008). MFG-E8 has been shown to facilitate phagocytic removal of apoptotic cells by acting as a bridging molecule between phosphatidylserine exposed on the apoptotic cell and αvβ3/5 integrin receptors on phagocytes. This enhanced clearance of apoptotic cells prevents secondary necrosis which could release proinflammatory mediators leading to tissue damage (Hanayama et al. 2002), MFG-E8 also exerts other beneficial effects in tissue injury such as suppression of inflammation and apoptosis in intestinal ischemia (Cui et al. 2010) and Alzheimer's disease (Fuller and Van Eldik 2008).
Previous studies have shown that administration of rat MFG-E8-containing exosomes or recombinant murine MFG-E8 (rmMFG-E8) increases phagocytosis of apoptotic cells, reduces proinflammatory cytokines, and improves survival in a rat model of sepsis induced by cecal ligation of puncture (CLP) (Miksa, et al., 2008; Miksa, et al., 2009c). However, one obstacle hampering the development of MFG-E8 as a therapeutic agent for patients is the potential immunogenicity of animal proteins in humans.
The present invention addresses the need for treatment of cerebral ischemia and sepsis as well as other diseases and disorders, using in particular recombinant human MFG-E8 (rhMFG-E8).
The present invention provides methods of preventing and/or treating cerebral ischemia in a subject comprising administering to the subject a milk fat globule epidermal growth factor-factor VIII (MFG-E8) in an amount effective to prevent and/or treat cerebral ischemia.
The invention also provides methods of preparing pharmaceutical compositions for preventing and/or treating cerebral ischemia, the methods comprising formulating milk fat globule epidermal growth factor-factor VIII (MFG-E8) in a pharmaceutical composition in an amount effective to prevent and/or treat cerebral ischemia.
The invention also provides pharmaceutical compositions comprising milk fat globule epidermal growth factor-factor VIII (MFG-E8) in dosage form for preventing and/or treating cerebral ischemia, and a pharmaceutically acceptable carrier.
The invention further provides pharmaceutical products comprising a milk fat globule epidermal growth factor-factor VIII (MFG-E8) formulated in a pharmaceutically acceptable carrier; and a package insert providing instructions for the administration of MFG-E8 for the prevention and/or treatment of cerebral ischemia.
The invention also provides recombinant human MFG-E8 (rhMFG-E8) having an amino acid sequence that is at least 95% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1), wherein the rhMFG-E8 is non-glycosylated.
The invention also provides methods of preventing and/or treating inflammation and/or organ injury after ischemia/reperfusion in a subject comprising administering to the subject a recombinant human milk fat globule epidermal growth factor-factor VIII (rhMFG-E8) in an amount effective to prevent and/or treat inflammation and/or organ injury, wherein the rhMFG-E8 has an amino acid sequence that is at least 95% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1) and wherein the rhMFG-E8 is non-glycosylated.
The invention further provides methods of treating a subject having sepsis or a subject at risk for sepsis, the methods comprising administering to the subject an amount of a recombinant human milk fat globule epidermal growth factor-factor VIII (rhMFG-E8) effective to reduce a physiologic effect of sepsis, wherein the rhMFG-E8 has an amino acid sequence that is at least 95% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1) and wherein the rhMFG-E8 is non-glycosylated.
The invention also provides methods of treating lung injury in a subject comprising administering to the subject an amount of a recombinant human milk fat globule epidermal growth factor-factor VIII (rhMFG-E8) effective to treat lung injury, wherein the rhMFG-E8 has an amino acid sequence that is at least 95% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1) and wherein the rhMFG-E8 is non-glycosylated.
Also provided are methods of preparing a pharmaceutical composition for preventing and/or treating inflammation and/or organ injury after ischemia/reperfusion in a subject, the methods comprising formulating a recombinant human milk fat globule epidermal growth factor-factor VIII (rhMFG-E8) in a pharmaceutical composition in an amount effective to prevent and/or treat inflammation and/or organ injury after ischemia/reperfusion, wherein the rhMFG-E8 has an amino acid sequence that is at least 95% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1) and wherein the rhMFG-E8 is non-glycosylated.
Also provided are methods of preparing a pharmaceutical composition for treating a subject having sepsis or a subject at risk for sepsis, the methods comprising formulating a recombinant human milk fat globule epidermal growth factor-factor VIII (rhMFG-E8) in a pharmaceutical composition in an amount effective to reduce a physiologic effect of sepsis, wherein the rhMFG-E8 has an amino acid sequence that is at least 95% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1) and wherein the rhMFG-E8 is non-glycosylated.
Further provided are methods of preparing a pharmaceutical composition for treating lung injury in a subject, the methods comprising formulating a recombinant human milk fat globule epidermal growth factor-factor VIII (rhMFG-E8) in a pharmaceutical composition in an amount effective to treat lung injury, wherein the rhMFG-E8 has an amino acid sequence that is at least 95% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1) and wherein the rhMFG-E8 is non-glycosylated.
Also provided are pharmaceutical compositions comprising a recombinant human milk fat globule epidermal growth factor-factor VIII (rhMFG-E8) in dosage form for preventing and/or treating inflammation and/or organ injury after ischemia/reperfusion, and a pharmaceutically acceptable carrier, wherein the rhMFG-E8 has an amino acid sequence that is at least 95% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1) and wherein the rhMFG-E8 is non-glycosylated.
Also provided are pharmaceutical compositions comprising a recombinant human milk fat globule epidermal growth factor-factor VIII (rhMFG-E8) in dosage form for treating a subject having sepsis or a subject at risk for sepsis, and a pharmaceutically acceptable carrier, wherein the rhMFG-E8 has an amino acid sequence that is at least 95% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1) and wherein the rhMFG-E8 is non-glycosylated.
Further provided are pharmaceutical compositions comprising a recombinant human milk fat globule epidermal growth factor-factor VIII (rhMFG-E8) in dosage form for treating lung injury, and a pharmaceutically acceptable carrier, wherein the rhMFG-E8 has an amino acid sequence that is at least 95% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1) and wherein the rhMFG-E8 is non-glycosylated.
Also provided are pharmaceutical products comprising a recombinant human milk fat globule epidermal growth factor-factor VIII (rhMFG-E8) formulated in a pharmaceutically acceptable carrier; and a package insert providing instructions for the administration of rhMFG-E8 for the prevention and/or treatment of inflammation and/or organ injury after ischemia/reperfusion, wherein the rhMFG-E8 has an amino acid sequence that is at least 95% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1) and wherein the rhMFG-E8 is non-glycosylated.
Also provided are pharmaceutical products comprising a recombinant human milk fat globule epidermal growth factor-factor VIII (rhMFG-E8) formulated in a pharmaceutically acceptable carrier; and a package insert providing instructions for the administration of rhMFG-E8 for treating a subject having sepsis or a subject at risk for sepsis, wherein the rhMFG-E8 has an amino acid sequence that is at least 95% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1) and wherein the rhMFG-E8 is non-glycosylated.
Further provided are pharmaceutical products comprising a recombinant human milk fat globule epidermal growth factor-factor VIII (rhMFG-E8) formulated in a pharmaceutically acceptable carrier; and a package insert providing instructions for the administration of rhMFG-E8 for the treatment of lung injury, wherein the rhMFG-E8 has an amino acid sequence that is at least 95% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1) and wherein the rhMFG-E8 is non-glycosylated.
a-4b. rhMFG-E8 reduced thymocyte apoptosis after CLP. Rats underwent CLP to induce experimental sepsis and were treated with human albumin (Vehicle), rmMFG-E8 (20 μg/kg BW), or rhMFG-E8 (20 μg/kg BW) immediately after CLP. (A) Thymocyte apoptosis was assessed 20 h after CLP by Annexin V/PI staining and FACS analysis. Data are presented as means±SE (n=4/group) and compared by one-way ANOVA and Student-Newman-Keuls Method: *P<0.05 vs. Sham group; #P<0.05 vs. Vehicle group. (B) Alterations in cleaved caspase-3 in the thymus were determined by Western Blot at 20 h after CLP. Representative gels of 2 independent observations are presented.
a-5b. rhMFG-E8 attenuated organ injury after CLP. Rats underwent CLP to induce experimental sepsis and were treated with human albumin (Vehicle), rmMFG-E8 (20 μg/kg BW), or rhMFG-E8 (20 μg/kg BW) immediately after CLP. Serum levels of lactate (A) and IL-6 (B) were measured at 20 h after CLP. Data are presented as means±SE (n=4-6/group) and compared by one-way ANOVA and Student-Newman-Keuls Method: *P<0.05 vs. Sham group; #P<0.05 vs. Vehicle group.
a-9c. Alterations in infarct size and cerebral histopathology in sham-operated rats (Sham) compared with vehicle and rhMFG-E8 treated after cerebral ischemia. (a) 2 mm thick coronal slices of fresh brain tissue were stained with triphenyl tetrazolium chloride (ITC) and digitally analyzed with NIH ImageJ software. Representative images of TTC staining are shown at the top of the bars. Data are presented as mean±SE, and analyzed by Student's t-test. Treatment with rhMFG-E8 decreased infarct size compared with Vehicle (n=6, *p<0.05 vs. Vehicle). (b) Photomicrographs of hematoxylin-eosin (H & E) stained slides were obtained by scanning slides (A, C, E), and by bright field microscopy at 400× original magnification (B, D, F). Sham (A, B) shows only normal viable basophilic neurons (shown by arrow heads). Vehicle group (C, D) shows mainly necrotic eosinophilic neurons (shown by long arrows), rhMFG-E8 treatment (E, F) protects against neuronal necrosis resulting in a mix of viable basophilic neurons and necrotic eosinophilic neurons. Scale bar=50 μm. (c) The average number of intact neurons (basophilic neurons) in six random fields per H & E stained slide was determined. Data are presented as mean±SE, and analyzed by Kruskal-Wallis one-way ANOVA. Cerebral ischemia (MCAO) caused significant reduction in number of intact neurons in both Vehicle and rhMFG-E8 treated animals compared with Sham animals. rhMFG-E8 treatment protected neurons against necrosis (n=6, *p<0.05 vs. Sham, #p<0.05 vs. Vehicle).
a-10d. Alterations in cerebral IL-6, TNFα, and myeloperoxidase in sham-operated rats (Sham) compared with vehicle and rhMFG-E8 treatment after cerebral ischemia. (a) Cerebral IL-6 levels were measured by ELISA at 24 h post-MCAO. Data are presented as mean±SE, and analyzed by one-way ANOVA and Student Newman Keul's method. Cerebral ischemia (MCAO) caused elevation of IL-6 levels in both Vehicle and rhMFGE8-treated animals compared with Sham animals. Treatment with rhMFG-E8 downregulated IL-6 expression compared with Vehicle (n=6, *p<0.05 vs. Sham, #p<0.05 vs. Vehicle). (b) Brain tissue was immunohistochemically stained for TNF-α and examined at 400× original magnification under bright field microscopy. Vehicle (B) and rhMFG-E8 (C) treated animals showed increased expression of TNF-α compared with Sham animals (A). rhMFG-E8 treatment (C) decreased TNF-α expression compared with Vehicle (B). Scale bar=50 μm. (c) Brain issue immunohistochemically stained for neutrophil marker, myeloperoxidase, and examined under bright field microscopy at 400× original magnification. Sham (A) animals showed no staining for myeloperoxidase (no neutrophil infiltration) whereas Vehicle (B) and rhMFG-E8 (C) treated animals showed staining for myeloperoxidase. rhMFG-E8 treatment (C) after cerebra ischemia decreased myeloperoxidase staining compared with Vehicle (B). Scale bar=50 μm. (d) Quantification of cerebral neutrophil infiltration by myeloperoxidase immunohistochemistry. Neutrophils were identified as small, round, myeloperoxidase-staining cells on bright field microscopy at 400× original magnification. The average number of neutrophils in six random fields per slide was determined as neutrophil count/40× high power field (hpf). Data are presented as mean±SE, and analyzed by oneway ANOVA and Student Newman Keul's method. Compared with Sham animals, Vehicle arid rhMFG-E8 treated animals showed increased neutrophil infiltration. rhMFGE8 treatment decreased cerebral neutrophil infiltration compared with vehicle (n=4, *p<0.05 vs. Sham, #p<0.05 vs. Vehicle).
a-11b. Alteration in ICAM-1 and peroxisome proliferator activated receptor-γ (PPAR-γ) expression after cerebral ischemia. (a) Cerebral ICAM-1 gene expression was measured by RT-PCR. Data are presented as mean±SE, and analyzed by one-way ANOVA and Student Newman Keul's method. Cerebral ischemia resulted in upregulation of ICAM-1 expression in Vehicle compared with Sham. rhMFG-E8 treatment decreased ICAM-1 expression, even though not significant compared with Vehicle (n=4-6, *p<0.05 vs. Sham). (b) PPAR-γ protein levels were determined by western blot at 24 h post-MCAO. Data are presented as mean±SE, and analyzed by Kruskal-Wallis one-way ANOVA. Compared with Sham, cerebral ischemia downregulated PPAR-γ in the Vehicle group. rhMFG-E8 treatment upregulated PPAR-γ expression compared with Vehicle (n=6, *p<0.05 vs. Sham, #p<0.05 vs. Vehicle).
a-12c. The effects of rhMFG-E8 treatment on apoptosis, measured by Bcl-2/Bax ratio and TUNEL staining, after cerebral ischemia in rats. (a) Bcl-2/Bax ratio was determined by western blot. Data are presented as means±SE, and analyzed by one-way ANOVA and Student Newman Keul's method. The Bcl-2/Bax ratio was not different between Vehicle and Sham. rhMFG-E8 treatment significantly elevated Bcl-2/Bax ratio compared with Vehicle and Sham (n=6, *p<0.05 vs. Vehicle and Sham), (b) TUNEL staining after cerebral ischemia. On fluorescent microscopy at 200× original magnification, apoptotic cells appeared as brighter fluorescent while propidium iodide (PI) darker staining showed the nuclear location of the TUNEL reaction products. The Sham group (A, B, C) showed no apoptosis since there were no positive cells on TUNEL staining (A). The Vehicle group (D, E, F) shows increased apoptosis as shown by increased number of TUNEL positive cells (D). A merge (F) of TUNEL staining (D) and PI staining (E) shows that most of the cells in the penumbra of Vehicle animals were apoptotic. Treatment with rhMFG-E8 (G, H, I) decreased apoptosis as shown by less TUNEL staining (G) compared with Vehicle TUNEL staining (D). A merge (I) of the rhMFG-E8 TUNEL staining (G) and PI staining (H) shows that rhMFG-E8 treatment protected brain cells from apoptosis compared with the Vehicle group (F). (c) Quantification of TUNEL staining. Eight random fields were captured at 200× original magnification for each slide. The average number of TUNEL positive cells were counted and expressed as TUNEL cells/20× high power field (hpf). Data are presented as mean±SE, and analyzed by oneway ANOVA and Student Newman Keul's method. Cerebral ischemia increased TUNEL-positive cells in Vehicle and rhMFG-E8 treated animals compared with Sham animals. Treatment with rhMFG-E8 decrease the number of TUNEL-positive cells compared with Vehicle group (n=4, *p<0.05, Sham, #p<0.05 vs. Vehicle).
The present invention provides methods of preventing and/or treating cerebral ischemia in a subject comprising administering to the subject a milk fat globule epidermal growth factor-factor VIII (MFG-E8) in an amount effective to prevent and/or treat cerebral ischemia.
The subject can be, for example, a subject having cerebral ischemia or a patient at risk for cerebral ischemia, for example, a patient who is undergoing or about to undergo surgery. The cerebral ischemia can be. for example, a focal brain ischemia caused by a blood clot that occludes a cerebral blood vessel, or global brain ischemia caused by reduced blood flow to the brain.
As used herein, to “treat” cerebral ischemia in a subject means to prevent or reduce a physiological effect of cerebral ischemia. For example, administration of MFG-E8 to the subject can reduce cerebral level of interleukin-6 (IL-6), and/or reduce numbers of infiltrated neutrophils, and/or reduce cerebral inflammation and/or apoptosis. Preferably, administration of MFG-E8 reduces and/or prevents death of brain tissue. Preferably, the chance of survival of the subject is increased by the administration of MFG-E8.
The invention also provides a method of preparing a pharmaceutical composition for preventing and/or treating cerebral ischemia, the method comprising formulating milk fat globule epidermal growth factor-factor VIII (MFG-E8) in a pharmaceutical composition in an amount effective to prevent and/or treat cerebral ischemia.
The invention also provides a pharmaceutical composition comprising milk fat globule epidermal growth factor-factor VIII (MFG-E8) in dosage form for preventing and/or treating cerebral ischemia, and a pharmaceutically acceptable carrier.
The invention further provides a pharmaceutical product comprising a milk fat globule epidermal growth factor-factor VIII (MFG-E8) formulated in a pharmaceutically acceptable carrier; and a package insert providing instructions for the administration of MFG-E8 for the prevention and/or treatment of cerebral ischemia.
In a preferred embodiment of any of the methods, compositions, products or uses described herein, the MFG-E8 is a recombinant human MFG-E8 (rhMFG-E8). In different embodiments, the rhMFG-E8 has an amino acid sequence that is at least 95% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1), or that is at least 99% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1), or that is identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1). In a preferred embodiment, the MFG-E8 is non-glycosylated.
The invention also provides a recombinant human MFG-E8 (rhMFG-E8) having an amino acid sequence that is a least 95% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1), wherein the rhMFG-E8 is non-glycosylated.
The invention also provides a method of preventing and/or treating inflammation and/or organ injury after ischemia/reperfusion in a subject comprising administering to the subject a recombinant human milk fat globule epidermal growth factor-factor VIII (rhMFG-E8) in an amount effective to prevent and/or treat inflammation and/or organ injury, wherein the rhMFG-E8 has an amino acid sequence that is at least 95% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1) and wherein the rhMFG-E8 is non-glycosylated. The ischemia/reperfusion can be, the example, one or more of gastrointestinal tract, liver, lung, kidney, heart, brain, spinal cord or crushed limb ischemia/reperfusion.
Preferably, the method prevents or reduces serum elevation of one or more of tumor necrosis factor-α, interleukin-6, interleukin-1β, aspartate aminotransferase, alanine aminotransferase, lactate, or lactate dehydrogenase. Preferably, inflammation is prevented or treated. Preferably, organ injury is prevented or treated, where for example, the organ is one or more of gastrointestinal tract, liver, lung, kidney, heart, brain, spinal cord or crushed limb. Preferably, the chance of survival of the subject is increased.
The invention further provides a method of treating a subject having sepsis or a subject at risk for sepsis, the method comprising administering to the subject an amount of a recombinant human milk fat globule epidermal growth factor-factor VIII (rhMFG-E8) effective to reduce a physiologic effect of sepsis, wherein the rhMFG-E8 has an amino acid sequence that is at least 95% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1) and wherein the rhMFG-E8 is non-glycosylated. The physiologic effect of sepsis can be, for example, elevation of serum TNF-α levels, and/or elevation of serum IL-6 levels, and/or shock. Preferably, administration of rhMFG-E8 attenuates systemic inflammation.
The invention also provides a method of treating lung injury in a subject comprising administering to the subject an amount of a recombinant human milk fat globule epidermal growth factor-factor VIII (rhMFG-E8) effective to treat lung injury, wherein the rhMFG-E8 has an amino acid sequence that is an least 95% identical in human MFG-E8 (hMFG-E8) (SEQ ID NO:1) and wherein the rhMFG-E8 is non-glycosylated. In a preferred embodiment, the lung injury is an acute lung injury.
The use of forms of MFG-E8 other than the rhMFG-E8 disclosed herein for treating sepsis, ischemia/reperfusion and lung injury have been described (US 2009/0297498, WO 2009/064448).
The invention also provides a method of preparing a pharmaceutical composition for preventing and/or treating inflammation and/or organ injury after ischemia/reperfusion in a subject, the method comprising formulating a recombinant human milk fat globule epidermal growth factor-factor VIII (rhMFG-E8) in a pharmaceutical composition in an amount effective to prevent and/or treat inflammation and/or organ injury after ischemia/reperfusion, wherein the rhMFG-E8 has an amino acid sequence that is at least 95% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1) and wherein the rhMFG-E8 is non-glycosylated.
The invention also provides a method of preparing a pharmaceutical composition for treating a subject having sepsis or a subject at risk for sepsis, the method comprising formulating a recombinant human milk fat globule epidermal growth factor-factor VIII (rhMFG-E8) in a pharmaceutical composition in an amount effective to reduce a physiologic effect of sepsis, wherein the rhMFG-E8 has an amino acid sequence that is at least 95% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1) and wherein the rhMFG-E8 is non-glycosylated.
The invention further provides a method of preparing a pharmaceutical composition for treating lung injury in a subject, the method comprising formulating a recombinant human milk fat globule epidermal growth factor-factor VIII (rhMFG-E8) in a pharmaceutical composition in an amount effective to treat lung injury, wherein the rhMFG-E8 has an amino acid sequence that is at least 95% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1) and wherein the rhMFG-E8 is non-glycosylated.
The invention also provides a pharmaceutical composition comprising a recombinant human milk fat globule epidermal growth factor-factor VIII (rhMFG-E8) in dosage form for preventing and/or treating inflammation and/or organ injury after ischemia/reperfusion, and a pharmaceutically acceptable carrier, wherein the rhMFG-E8 has an amino acid sequence that is at least 95% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1) and wherein the rhMFG-E8 is non-glycosylated.
The invention also provides a pharmaceutical composition comprising a recombinant human milk fat globule epidermal growth factor-factor VIII (rhMFG-E8) in dosage form for treating a subject having sepsis or a subject at risk for sepsis, and a pharmaceutically acceptable carrier, wherein the rhMFG-E8 has an amino acid sequence that is at least 95% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1) and wherein the rhMFG-E8 is non-glycosylated.
The invention further provides a pharmaceutical composition comprising a recombinant human milk fat globule epidermal growth factor-factor VIII (rhMFG-E8) in dosage form for treating lung injury, and a pharmaceutically acceptable carrier, wherein the rhMFG-E8 has an amino acid sequence that is a least 95% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1) and wherein the rhMFG-E8 is non-glycosylated.
The invention also provides a pharmaceutical product comprising a recombinant human milk fat globule epidermal growth factor-factor VIII (rhMFG-E8) formulated in a pharmaceutically acceptable carrier; and a package insert providing instructions for the administration of rhMFG-E8 for the prevention and/or treatment of inflammation and/or organ injury after ischemia/reperfusion, wherein the rhMFG-E8 has an amino acid sequence that is at least 95% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1) and wherein the rhMFG-E8 is non-glycosylated.
The invention also provides a pharmaceutical product comprising a recombinant human milk fat globule epidermal growth factor-factor VIII (rhMFG-E8) formulated in a pharmaceutically acceptable carrier; and a package insert providing instructions for the administration of rhMFG-E8 for treating a subject having sepsis or a subject at risk for sepsis, wherein the rhMFG-E8 has an amino acid sequence that is at least 95% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1) and wherein the rhMFG-E8 is non-glycosylated.
The invention further provides a pharmaceutical product comprising a recombinant human milk fat globule epidermal growth factor-factor VIII (rhMFG-E8) formulated in a pharmaceutically acceptable carrier; and a package insert providing instructions for the administration of rhMFG-E8 for the treatment of lung injury, wherein the rhMFG-E8 has an amino acid sequence that is at least 95% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1) and wherein the rhMFG-E8 is non-glycosylated.
The invention also provides for the use of a milk fat globule epidermal growth factor-factor VIII (MFG-E8) for the preparation of a medicament for the prevention and/or treatment of cerebral ischemia, as well as a milk fat globule epidermal growth factor-factor VIII (MFG-E8) for use for preventing and/or treating cerebral ischemia.
The invention further provides for the use of a recombinant human milk fat globule epidermal growth factor-factor VIII (rhMFG-E8) for the preparation of a medicament for the prevention and/or treatment of inflammation and/or organ injury after ischemia/reperfusion, or for the treatment of a subject having sepsis or a subject at risk for sepsis, or for the treatment of lung injury, wherein the rhMFG-E8 has an amino acid sequence that is at least 95% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1) and wherein the rhMFG-E8 is non-glycosylated, as well providing rhMFG-E8 for use for preventing and/or treating inflammation and/or organ injury after ischemia/reperfusion, or for treating a subject having sepsis or a subject at risk for sepsis, or for treating lung injury in a subject.
In different embodiments of the recombinant human MFG-E8, methods, compositions, products, or uses the rhMFG-E8 has an amino acid sequence that is at least 99% identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1) or the rhMFG-E8 has an amino acid sequence that is identical to human MFG-E8 (hMFG-E8) (SEQ ID NO:1).
MFG-E8 can be administered to the subject in a pharmaceutical composition comprising a pharmaceutically acceptable carrier. Examples of acceptable pharmaceutical carriers include, but are not limited to, additive solution-3 (AS-3), saline, phosphate buffered saline, Ringer's solution, lactated Ringer's solution, Locke-Ringer's solution, Krebs Ringer's solution, Hartmann's balanced saline solution, and heparinized sodium citrate acid dextrose solution.
Compositions comprising MFG-E8 can be formulated without undue experimentation for administration to a subject, including humans, as appropriate for the particular application. Additionally, proper dosages of the compositions can be determined without undue experimentation using standard dose-response protocols.
Accordingly, the compositions designed for oral, lingual, sublingual, buccal and intrabuccal administration can be made without undue experimentation by means well known in the art, for example with an inert diluent or with an edible carrier. The compositions may be enclosed in gelatin capsules or compressed into tablets. For the purpose of oral therapeutic administration, the pharmaceutical compositions of the present invention may be incorporated with excipients and used in the form of tablets, troches, capsules, elixirs, suspensions, syrups, wafers, chewing gums and the like.
Tablets, pills, capsules, troches and the like may also contain binders, recipients, disintegrating agent, lubricants, sweetening agents, and flavoring agents. Some examples of binders include microcrystalline, cellulose, gum tragacanth or gelatin. Examples of excipients include starch or lactose. Some examples of disintegrating agents include alginic acid, corn starch and the like. Examples of lubricants include magnesium stearate or potassium stearate. An example of a glidant is colloidal silicon dioxide. Some examples of sweetening agents include sucrose, saccharin and the like. Examples of flavoring agents include peppermint, methyl salicylate, orange flavoring and the like. Materials used in preparing these various compositions should be pharmaceutically pure and nontoxic in the amounts used.
The compositions of the present invention can easily be administered parenterally such as for example, by intravenous, intramuscular, intrathecal or subcutaneous injection. Parenteral administration can be accomplished by incorporating the compositions of the present invention into a solution or suspension. Such solutions or suspensions may also include sterile diluents such as water for injection, saline solution, fixed oils, polyethylene glycols, glycerine, propylene glycol or other synthetic solvents. Parenteral formulations may also include antibacterial agents such as for example, benzyl alcohol or methyl parabens, antioxidants such as for example, ascorbic acid or sodium bisulfite and chelating agents such as EDTA. Buffers such as acetates, citrates or phosphates and agents for the adjustment of tonicity such as sodium chloride or dextrose may also be added. The parenteral preparation can be enclosed in ampules, disposable syringes or multiple dose vials made of glass or plastic.
Rectal administration includes administering the pharmaceutical compositions into the rectum or large intestine. This can be accomplished using suppositories or enemas. Suppository formulations can easily be made by methods known in the art. For example, suppository formulations can be prepared by heating glycerin to about 120° C., dissolving the composition in the glycerin, mixing the heated glycerin after which purified water may be added, and pouring the hot mixture into a suppository mold.
Transdermal administration includes percutaneous absorption of the composition through the skin. Transdermal formulations include patches (such as the well-known nicotine patch), ointments, creams, gels, salves and the like.
The present invention includes nasally administering to the mammal a therapeutically effective amount of the composition. As used herein, nasally administering or nasal administration includes administering the composition to the mucous membranes of the nasal passage or nasal cavity of the patient. As used herein, pharmaceutical compositions for nasal administration of a composition include therapeutically effective amounts of the composition prepared by well-known methods to be administered, for example, as a nasal spray, nasal drop, suspension, gel, ointment, cream or powder. Administration of the composition may also take place using a nasal tampon or nasal sponge.
The subject can be a human or another animal.
Amino acid sequences for human and mouse MFG-E8 are shown below.
Human MGF-E8 protein is synthesized as the 387 amino acid precursor shown above that contains a 23 amino acid signal sequence and a 364 amino acid mature region. The recombinant human protein expressed in this study is the mature molecule of human MFG-E8 (i.e., Leu24-Cys387), i.e., amino acids 24 through 387 of SEQ ID NO:2, which is herein referred to a SEQ ID NO:1.
This invention will be better understood from the Experimental Details, which follow. However, one skilled in the art will readily appreciate that the specific methods and results discussed are merely illustrative of the invention as described more fully in the claims that follow thereafter.
A 1095 bp fragment (SEQ ID NO:3) encoding the mature region of human MFG-E8 (364 amino acids, R24-R387, SwissProt #: Q08431) was obtained by polymerase chain reaction amplification of a plasmid template containing the human MFG-E8 cDNA. The open reading frame was cloned into the Sal I and Not I site of the pET-28a(+) vector (Novagen, Madison, Wis.) downstream of the phage T7 RNA polymerase promoter. The final protein product contains six histidines fused to the N-terminus of human MFG-E8. The plasmid was transformed into E. coli BL21 (DE3) cells. The cells were grown at 37° C. in 2YT medium (Invitrogen) with kanamycin overnight. The rhMFG-E8 protein production was induced by the addition of isopropyl-β-D-thiogalactopyranoside (IPTG) to a final concentration of 1.0 mM and cells growth continued for 5 h at 25° C. The cells were harvested by centrifugation and the induced rhMFG-E8 protein was purified according to the manufacture's instruction (Novagen). The rhMFG-E8 fractions were pooled and endotoxin of protein solution was removed by phase separation using Triton X-114 (Aida and Pabst. 1990). The content of LPS in the sample was determined using the Limulus amebocyte lysate assay (BioWhittaker Inc, Walkersville, Md.) are described previously (Li, et al., 2004). The purity of rhMFG-E8 was evaluated by SDS-PAGE on a 10-20% Tris-HCl gel and visualized using GelCode Blue Stain Regent (Pierce, Rockford Ill.). The final product was concentrated by Amicon Ultra-15 Centrifugal Filter Devices to designed concentration and stored at −20° C. Human MFG-E8 encoding DNA sequence minus the signal peptide (SEQ ID NO:4):
The amino acid sequence of the isolated and purified protein was analyzed by LC-MS/MS at the Proteomics Resource Center of the Rockefeller University (New York, N.Y.). Briefly, the sample was reduced with 5 mM of DTT and alkylated with 10 mM iodoacetamide, and then digested with Sequence Grade Modified Trypsin (Promega) in ammonium bicarbonate buffer at 37° C. overnight. The digestion products were analyzed by LC-MS/MS. For LC-MS/MS analysis, the digestion product was separated by gradient elution with the Dionex capillary/nano-HPLC system and analyzed by Applied Biosystems QSTAR XL mass spectrometer using information-dependent, automated acquisition. The acquired ms/ms spectra were converted to a MASCOT acceptable format and searched using the Mascot database search algorithm. The allowed variable modifications for database searching were oxidation of methionines.
Western Blot Analysis of rhMFG-E8
Purified rhMFG-E8 proteins were electrophoretically fractionated on a 10-20% Tris-HCl gel under reducing conditions, transferred to a 0.45-μm nitrocellulose membrane, and blocked with 5% nonfat dry milk in phosphate-buffered saline. Afterward, the membrane was incubated with 1:1000 polyclonal antibody to human MFG-E8 (R & D Systems, Minneapolis, Minn.) overnight at 4° C. The blots were then incubated with horseradish peroxidase-linked anti-rabbit immunoglobulin G (1:10000, Cell Signaling Technology, Beverly, Mass.) for 1 h at room temperature. A chemiluminescent peroxidase substrate (ECL, Amersham Biosciences, Piscataway, N.J.) was applied according to the manufacturer's instructions, and the membranes were exposed briefly to radiography film.
This assay was conducted as previously described (Miksa, et al., 2009a). Briefly, freshly collected peritoneal macrophages from normal adult Sprague-Dawley rats were cultured in Dulbecco's Modified Eagle's Medium (DMEM; GIBCO Life Technologies, Carlsbad, Calif.) containing 10% heat-inactivated exosome-free fetal bovine serum (FBS), 10 mM 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES), 100 U/ml penicillin and 100 mg/ml streptomycin at 37° C. in a humidified atmosphere containing 5% CO2. Cells were plated at a density of 2.5×104/well in a 16-well chamber slide (Nunc International, Rochester, N.Y.). For all experiments, cells were kept at 80-90% confluence. Freshly collected thymocytes were cultured at a concentration of 107 cells/ml in RPMI substituted with 10% heat-inactivated FBS, 10 mM HEPES, 100 U/ml penicillin, 100 mg/ml streptomycin, and 0.1 μM dexamethasone for 16-24 h at 37° C. and 5% CO2. This produced ˜100% apoptotic cells as assessed by annexin V/propidium iodide (PI) staining and analyzed by FACS. After being washed twice with Hank's balanced salt solution (HBSS, GIBCO), the apoptotic thymocytes were resuspended in OPTI-MEM (GIBCO) and incubated with or without rhMFG-E8 (0.5 μg/ml) or rmMFG-E8 (0.5 μg/ml) for 30 min. Then the cells were incubated with 20 ng/ml pHrodo-Se (Invitrogen) for 30 min. After washing, the cells were fed to cultured macrophages at the ratio of 4:1 (apoptotic cells/macrophages) for 1.0 h. Then, adherent macrophages were washed twice with PBS and incubated with FITC-anti-rat CD11b/c (OX42; BD pharmingen) for 20 min. This staining provided a homogenous surface staining of macrophages and was useful to distinguish the surface of macrophages during analysis. The cells were then fixed with 1% paraformaldehyde for 15 min at 4° C., transferred to PBS and kept at 4° C. until analysis by fluorescent microscopy using a Nikon Eclipse E600 florescent microscope (Japan). The number of apoptotic cells and of macrophages that engulfed apoptotic cells were expressed as a ratio of apoptotic cells/macrophages (phagocytosis index).
Male Sprague-Dawley rats (275-325 g) were housed in a temperature-controlled room on a 12-h light/dark cycle and fed a standard Purina rat chow diet. Prior to the induction of sepsis, rats were fasted overnight, but allowed water ad libitum. Rats were anesthetized with isoflurane inhalation and the ventral neck, abdomen and groin were shaved and washed with 10% povidone iodine. Cecal ligation and puncture (CLP) was performed as previously described (Wu, et al., 2007b; Cui, et al., 2004; Wu, et al., 2007a). Briefly, a 2-cm midline abdominal incision was performed. The cecum was exposed, ligated just distal to the ileocecal valve to avoid intestinal obstruction, punctured twice with an 18-gauge needle, squeezed slightly to allow a small amount of fecal matter to flow from the holes, and then returned to the abdominal cavity, following which the abdominal incision was closed in layers. Immediately after CLP, a femoral vein were cannulated with a PE-50 tubing under anesthesia (isoflurane inhalation). The animal received a bolus injection of rhMFG-E8 (20 μg/kg BW) in a volume of 1-ml normal saline via the femoral venous catheter. Positive control animals received commercial rmMFG-E8 (20 μg/kg BW). Vehicle-treated animals received a non-specific human plasma protein (i.e., human albumin) at the time of CLP. Sham-operated animals (i.e., control animals) underwent the same procedure with the exception that the cecum was neither ligated nor punctured. The animals were resuscitated with 3 ml/100 g BW normal saline subcutaneously immediately after surgery. The animals were then returned to their cages. All experiments were performed in accordance with the National Institutes of Health guidelines for the use of experimental animals. This project was approved by the Institutional Animal Care and Use Committee (IACUC) of The Feinstein Institute for Medical Research.
Thymocyte apoptosis was assessed by annexin V/propidium iodide (PI) staining and Western blot analysis of cleaved caspase-3 protein expression. Briefly, the fresh thymus was harvested at 20 h after CLP or sham operation. Thymocytes were isolated as described previously (Miksa, et al., 2009b). The cells were stained using the Annexin V Fluos staining kit (Boehringer Mannheim, Indianapolis, Ind.) according to the manufacturer's instruction and analyzed by flow cytometry with FACSCalibur (BD Biosciences). The annexin V+-PI− cells were considered as apoptotic cells. Cleaved caspase-3 protein expression was measured by Western blot analysis similar to the method for rhMFG-E8 protein analysis, as described above. Specific antibodies against cleaved caspase-3 protein (Cell Signaling, Danvers, Mass.) were used. β-Actin was acid as the loading control.
Serum concentrations of lactate were determined by using the assay kit according to the manufacturer's instructions (Pointe Scientific, Lincoln Park, Mich.). Serum levels of IL-6 were measured using a commercially available enzyme-linked immunosorbent assay (ELISA) kit (BioSource International, Camarillo, Calif.) according to the manufacturer's instruction.
In additional groups of animals, vehicle (human albumin), rhMFG-E8 or rmMFG-E8 (20 μg/kg BW) was administered immediately after CLP as described above. At 20 h after CLP, the gangrenous cecum was surgically excised and the peritoneal cavity was irrigated twice with 20 ml warm, sterile saline solution. The abdominal incision was then closed in layers, and rats received 3 ml/100 g BW saline subcutaneously. The animals were then returned to their cages and allowed food and water ad libitum. The charges in survival were monitored for 10 days.
All data are expressed as means±SE and compared by one-way analysis of variance (ANOVA). When the ANOVA was significant, post-hoc testing of differences between groups was performed using Student-Newman-Keuls method. The survival rate was estimated by Kaplan-Meier method and compared by the log-rank test. A P value<0.05 was considered statistically significant.
Expression and Purification of rhMFG-E8
Using the E. coli system, rhMFG-E8 was successfully expressed and purified. The SDS-PAGE analysis showed a single band at approximately 46 kDa (
rhMFG-E8 Increased the Phagocytosis of Apoptotic Cells in Vitro
Using peritoneal macrophages isolated from normal rats, rhMFG-E8 (0.5 μg/ml) was shown to markedly increase peritoneal macrophages' phagocytosis of apoptotic thymocytes as compared to medium control (P<0.05,
rhMFG-E8 Reduced Apoptosis and Tissue Injury in a Rat Model of Sepsis
To determine the biological activity of the newly-expressed rhMFG-E8 in vivo, its effect was tested in a rat model of CLP. As shown in
rhMFG-E8 Decreased Sepsis-Induced Mortality in Rats
To determine the long-term effect of rhMFG-E8 is sepsis, a 10-day survival study was conducted. As shown in
Sepsis is a common, expensive, and frequently fatal condition. Although a great deal of preclinical and clinical trials have been carried out testing the efficacy and safety of various anti-sepsis agents (e.g., anti-cytokine and anti-endotoxin antibodies, steroids, antithrombin, and insulin, inhibition of apoptosis, etc.), those investigations have not resulted in the development of effective clinical treatment (Ferrer, et al., 2008; Strehlow, et al., 2006; Martin, et al., 2003; Guidet, et al., 2005). Apoptosis plays an important role in the pathobiology of sepsis (Hotchkiss and Nicholson, 2006; Remick, 2007; Lang and Matute-Bello, 2009; Pinheiro da and Nizet, 2009; Ward, 2008; Ayala, et al., 2008). Reduction of apoptosis by over-expressing the anti-apoptotic Bcl-2 protein or inhibiting pro-apoptotic molecules such as caspases, Fas-ligand, TNF-R, or TRAIL has been proven to be beneficial in septic animals (Hotchkiss, et al., 2005; Wesche, et al., 2005; Wesche-Soldato, et al., 2005; Ayala, et al., 2003; Zhou, et al., 2004; Bommhardt, et al., 2004). In addition to the increased incidence of apoptosis, the phagocytic function is impaired in sepsis (Gregory and Wing, 2002; Zhang, et al., 1998; Gutierrez-Fernandez, et al., 1989; Angle, et al., 2000). Previous studies have shown that downregulation of MFG-E8 is responsible for the reduced phagocytosis of apoptotic cell in sepsis (Miksa, et al., 2008; Miksa, et al., 2009c). Administration of rat MFG-E8 containing exosomes or rmMFG-E8 increases phagocytosis of apoptotic cells, reduces proinflammatory cytokines, and improves survival in a rat model of sepsis (Miksa, et al., 2008; Miksa, et al., 2009c). The biologic effect of this molecules has been confirmed using the MFG-E8 knockout animal model (Miksa, et al., 2009c). Similarly, Bu et al. has shown that sepsis-triggered intestinal injury was associated with a downregulation of intestinal MFG-E8 and treatment with rmMFG-E8 promoted mucosal healing in septic mice (Bu, et al., 2007). Thus, MFG-E8 appears to be a leading candidate for treating septic patients.
Human MFG-E8 shares only 59%, 57%, and 53% amino acid (aa) sequence identity with porcine, rat, and mouse MFG-E8, respectively (blast.ncbi.nlm.nih.gov). In order to move this technology into clinical development, human MFG-E8 is required. However, the extremely high cost of commercial human MFG-E8 (using murine myeloma cell line by R & D Systems) limits its further development. In the current study, rhMFG-E8 was successfully expressed and purified using an E. coli system at a much lower cost (>95% less expensive). The human MFG-E8 gene is located on chromosome 15q25 and is composed of eight exons. Human MGF-E8 protein is synthesized as a 387 as precursor that contains a 23 as signal sequence and a 364 aa mature region. The protein expressed in this study is the mature molecule of human MFG-E8 (i.e., Leu24-Cys387) with an N-terminal 6 His tag. Native MFG-E8 is a glycoprotein. Since rhMFG-E8 was expressed in an E. coli system, it has no glycosylation. As demonstrated by this study, E. coli-derived rhMFG-E8 is as effective as the rmMFG-E8 expressed in the murine myeloma cell line (R & D). E. coli-derived rhMFG-E8 markedly increased peritoneal macrophages' phagocytosis of apoptotic thymocytes and reduced thymocyte apoptosis and plasma levels of lactate and IL-6 at 20 h after CLP. Most importantly, administration of E. coli-derived rhMFG-E8 improved the survival rate after CLP. Apparently, glycosylation may not be essential for the biological function of MFG-E8.
The mature molecule of human MFG-E8 contains four N-linked glycosylation sites, an amino-terminal EGF like domain, plus C1 and C2 Ig-like domains which are related to discoidin 1 and homologous to those of human coagulation factors V and VIII (Couto, et al., 1996; Taylor, et al., 1997). The EGF like domain contains the “RGD-motif” (the amino acid sequence: Arg-Gly-Asp), which is strategically placed in a hairpin loop between two antiparallel beta strands (Couto, et al., 1996; Taylor, et al., 1997). In this way, the EGF-like domain serves as a scaffold for the RGD sequence, which is proposed to promote cell adhesion by binding cell surface integrin receptors, such as αvβ3 or αvβ5 (Akakura, et al., 2004; Zullig and Hengartner, 2004; Ait-Oufella, et al., 2007). The coagulation factor V/VIII like domains bind to phosphatidylserine (PS) exposed on the surface of apoptotic cells (Veron, et al., 2005). Binding of MFG-E8 to PS on apoptotic cells opsonizes them for a complete engulfment by macrophages via αvβ3- or αvβ5-integrins. Without MFG-E8, full engulfment and the removal of apoptotic cells cannot be completed (Hanayama, et al., 2004). Apoptosis has been considered as an orderly process of cell suicide that does not elicit inflammation (Fadok, et al., 1998). However, recent discoveries have shown that apoptotic cells eventually undergo secondary necrosis and stimulate an inflammatory response if they are not removed by phagocytosis (Bell, et al., 2006; Scaffidi, et al., 2002). The lack of clearance of apoptotic B-cells in the spleen potentially leads to autoimmune diseases (Hanayama, et al., 2002; Hanayama, et al., 2004). Similar phenomena were also reported in the acute inflammatory environment such as sepsis (Hotchkiss, et al., 2003; Miksa et al., 2009c). In a recent study, pre-treatment of animals with apoptotic splenocytes worsens the outcome of sepsis (Hotchkiss, et al., 2003), pointing out the detrimental effect of apoptotic cells in the septic organism. The current study confirms the importance of apoptotic cell clearance in the pathogenesis of sepsis.
Male Sprague-Dawley rats (300-350 g), purchased from Charles River Laboratories (Wilmington, Mass.) were used in this study. The rats were housed under standard conditions (room temperature, 22° C., 12/12-h light/dark cycle) with regular access to standard Purina rat chow and water. The animals were allowed at least 5 days to acclimate under these conditions before being used for experiments. All animal experiments were performed in accordance with the National Institutes of Health guidelines for the use of experimental animals. This protocol was approved by the Institutional Animal Care and Use Committee (IACUC) of the Feinstein Institute for Medical Research.
Rats were fasted overnight but had access to water ad libitum before induction of cerebral ischemia. Permanent focal cerebral ischemia was induced by middle cerebral artery occlusion (MCAO) as previously described (Cheyuo et al., 2011; Zeng et al. 2010), with few modifications. Briefly, anesthesia was induced with 3.5% isoflurane and subsequently maintained by intravenous boluses of pentobarbital, not exceeding 30 mg/kg BW. Body temperature was maintained between 36.5° C. and 37.5° C. using a rectal temperature probe and a heating pad (Harvard Apparatus, Holliston, Mass.). The right common carotid artery (CCA) was exposed through a ventral midline neck incision and was carefully dissected free from the vagus nerve. The external carotid artery was then dissected and ligated. The internal carotid artery (ICA) was isolated and carefully separated from the adjacent vagus nerve, and the pterygopalatine artery was dissected and temporally occluded with a microvascular clip. Next, the CCA was ligated and an arteriotomy made just proximal to the bifurcation. A 2.5 cm length of 3-0 poly-L6 lysine coated monofilament nylon suture with a rounded tip was inserted through the arteriotomy into the ICA and advanced to the middle cerebral artery (MCA) origin to cause occlusion. Occlusion of the MCA was ascertained by inserting the suture to a predetermined length of 19-20 mm from the carotid bifurcation and feeling for resistance as the rounded suture tip approaches the proximal anterior cerebral artery which is of a relatively narrower caliber. The cervical wound was then closed in layers. One hour post-MCAO each rat was given an infusion of 1 ml saline as vehicle or 160 μg/kg BW rhMFG-E8 as treatment. Rats were then allowed to recover from anesthesia in a warm and quiet environment. The intraluminal suture was left in-situ and rats allowed unrestricted access to food and water until 24 h post-operatively when they were sacrificed. Brain tissues were rapidly collected for various anaylses. For histopathology, immunohistochemistry and terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL), rat brains were transcardially perfused with ice-cold normal saline followed by 4% paraformaldehyde before removal. Brain samples were then paraffinembedded and sectioned.
To establish a physiological basis for the use of MFG-E8 in the treatment of cerebral ischemia, changes in brain MFG-E8 levels after cerebral ischemia were assessed by Western blot. Briefly, protein obtained from brain homogenates of vehicle and sham groups were fractionated on a Bis-Tris gel and transferred to a 0.22 μm nitrocellulose membrane. Blots were blocked with 10% milk in Tris-buffered saline containing 0.1% vol/vol Tween 20 (TBST) and incubated with goat anti-MFG-E8 polyclonal IgG (1:100 in 10% BSA in TBST). After the incubation with horseradish peroxidase-labeled donkey anti-goat IgG (Santa Cruz Biotechnology Inc., Santa Cruz, Calif.) in 5% milk in TBST, and subsequently washing with TBST, bands were detected by chemiluminescence (GE Healthcare Biosciences, Piscataway, N.J.). The band densities were normalized by β-actin using the Bio-Rad imaging system.
Administration of rhMFG-E8
rhMFG-E8 was used as treatment in this study. rhMFG-E8 was expressed in-house using an E. coli system. The Ex-M0438-B01 expression clone for 6xHis-human MFG-E8 was purchased from GeneCopoeia, Inc (Germantown, Md.). The dose of rhMFG-E8 used in this study was chosen empirically based on previous experiments on dose-response effects of MFG-E8 in a sepsis model, which found the most efficacious dose to be 160 μg/kg BW (unpublished data).
Neurological deficits were determined at 24 h post-MCAO using a battery of sensorimotor and reflex behavioral tests as outlined in Table 1. Prior to MCAO, animals were trained in the various sensorimotor and reflex behavioral tasks for two days. A combined neuroscore was calculated as a summation of the scores in sensorimotor and reflex behavioral tasks. Full details of these tests have been described elsewhere (Flierl et al. 2009; Kawamata et al. 1996; Markgraf et al. 1992).
Infarct size was determined as previously described (Lu et al. 2010). Rats were euthanized under anesthesia at 24 h post-MCAO. The brains were rapidly removed and sectioned coronally into 2 mm-thick slices which were incubated in 2% triphenyl tetrazolium chloride at 37° C. for 30 min and then immersed in 10% formula overnight. The pale-appearing infarcted areas, as well as areas of the hemispheres were digitally analysed using NIH Image J software. The infarct volume and volumes of the hemispheres in each slice were calculated as the area multiplied by 2. The total infarct volume and hemispheric volumes for each rat brain were calculated as summation of the individual slices. An edema index was calculated by dividing the total volume of the right hemisphere (ischemic side) by the total volume of the left hemisphere (non-ischemic side). The actual infarct volume adjusted for edema was calculated by dividing the infarct volume by the edema index, and expressed as percentage of the total brain volume.
10 μm thick paraffin-embedded sections were stained with hematoxylin and eosin (H & E). The H & E stained slides were examined under bright field microscopy at 400× original magnification (Nikon Eclipse Ti microscope, Japan) for basophilic neurons, with purple-blue cytoplasm, and eosinophilic neurons, with pink cytoplasm, which are classified as intact neurons and necrotic neurons respectively (Ozden et al. 2011). Six images from six random visual fields were taken per slide. Quantification of intact neurons was performed while blinded to treatment allocations and functional outcomes. The average intact neuron count for each slide was expressed as intact neurons per 40× high power field.
Interleukin-6 (IL-6) levels in brain tissue lysates from the ipsilateral cerebral cortex were quantified by using commercially obtained enzyme-linked immunosorbent assay (ELISA) kits specific for IL-6 (BD BioSciences, San Jose, Calif.). The assay was carried out according to the instructions provided by the manufacturer.
6 μm paraffin sections of brain tissue were de-waxed and rehydrated, followed by microwave antigen retrieval procedure. Endogenous peroxidase and nonspecific binding sites were blocked using 2% H2O2 in 60% methanol and 3% normal goat serum respectively. The sections were then incubated with the following primary antibodies at room temperature for 2 h: rabbit anti-TNF-α polyclonal IgG (1:100, Millipore, Temecula, Calif.), and rabbit anti-MPO polyclonal IgG (1:100, Abcam, Cambridge, Mass.). The sections were then reacted with biotinylated anti-rabbit IgG, Vectastain ABC and DAB reagents (Vector Labs, Burlingame, Calif.). The immunohistochemical reaction was examined under light microscopy at 400× original magnification (Nikon E600 microscope, Japan). Neutrophils appeared as small, round, MPO-staining cells. Six images from six random fields in the penumbra of each slide were obtained. The average number of neutrophils was determined by NIH ImageJ particle analysis and expressed as neutrophils per 40× high power field.
Total RNA extracted from cerebral cortex by Tri-Reagent (Molecular Research Center, Cincinnati, Ohio) was reverse transcribed into cDNA and real-time PCR performed as previously described (Wu et al. 2009b). Briefly, ICAM-1 gene expression was determined from cDNA using murine leukemia virus reverse transcriptase in an Applied Biosystems 7300 real-time PCR system (Applied Biosystems, Foster City, Calif.). Expression amount of rat glyceraldehyde-3-phosphate dehydrogenase (GAPDH) mRNA was used for normalization of each sample. Relative expression of mRNA was calculated by the 2-ΔΔCt method, and results expressed as fold change with respect to control. The following rat primers were used: ICAM-1(NM—012967.1); Forward: 5′ CGA GTG GAC ACA ACT GGA AG 3′ (SEQ ID NO:5), Reverse: 5′ CGC TCT GGG AAC GAA TAC AC 3′ (SEQ ID NO:6).
Protein from homogenates of the ipsilateral cerebral cortex were fractionated on Bis-Tris gel and transferred to nitrocellulose membrane. Nitrocellulose blots were blocked in 5% milk in TBST (Tris-buffered saline Tween 20) and incubated overnight at 4° C. with the following rabbit polyclonal antibodies: anti-PPAR-γ (1:1000, Cayman Chemical, Ann Arbor, Mich.), anti-Bcl-2, and anti-Bax (1:500, Santa Cruz Biotechnology; Santa Cruz, Calif.). After reacting blots with HRP-labeled goat anti-rabbit IgG, protein bands were detected by chemiluminescence (GE Healthcare Biosciences, Piscataway, N.J.). The band densities were normalized by β-actin using the Bio-Rad imaging system.
6 μm paraffin sections of brain tissue were de-waxed and rehydrated, permeabilized with proteinase K, and then reacted with a green fluorescent-tagged enzyme solution (Roche Diagnostics, Indianapolis, Ind.). The slides were then washed with TBS, mounted with Vectashield medium with propidium iodide (Vector labs, Burlingame, Calif.) and examined under a fluorescence microscope (Nikon E600 microscope, Japan). Apoptotic cells appeared green fluorescent, and the nuclei which appeared red fluorescent confirmed the nuclear location of TUNEL products. Eight images were obtained from eight random visual fields in the penumbra of each slide at 200× original magnification. The average number of TUNEL positive cells for each slide was quantified by NIH ImageJ particle analysis and expressed as TUNEL positive cells per 2× high power field.
All data are expressed as means±SE and compared Student's ttest for two groups, and analysis of variance (ANOVA) and the Student-Newman-Keuls method for multiple groups. Differences in values were considered significant at p<0.05.
To determine whether permanent cerebral ischemia altered brain MFG-E8 levels, cerebral MFGE8 protein levels were measured at 24 h post-MCAO. As shown in
rhMFG-E8 Treatment Improve Neurological Function
MCAO induced sensorimotor and reflex behavioral deficits compared with baseline neurological function in sham animals. As shown as
rhMFG-E8 Decreases Infarct Size and Neuronal Necrosis
In the vehicle group, 24 hours of cerebral ischemia by MCAO caused infarction of 29.3% of the ipsilateral cerebral hemisphere. rhMFG-E8 treatment decreased the infarct size by 28.3% compared with vehicle (p<0.05,
rhMFG-E8 Suppresses Inflammation in Cerebral Ischemia
Compared with sham animals, MCAO resulted in elevations of cerebral IL-6 levels by 321% and 154% in vehicle and rhMFG-E8 treated animals respectively. Treatment with rhMFG-E8 decreased IL-6 levels by 39.6% compared with vehicle (p<0.05,
rhMFG-E8 Inhibits Apoptosis in Cerebral Ischemia
As shown in
The MFG-E8 gene, which in humans is located at the chromosomal position 15q25 (Collins et al. 1997), is ubiquitously expressed in various tissues, including the brain, in mammals (Aziz et al. 2009; Hanayama et al. 2004; Larocca et al. 1991). MFG-E8 plays physiological roles in cell-cell interaction through the binding of αvβ3/5 integrin receptors (Raymond et al. 2010). Under pathological conditions, MFG-E8 has been shown to promote clearance of apoptotic cells by binding phosphatidylserine exposed on the apoptotic cells and simultaneously engaging the αvβ3/5 integrin receptor on macrophages (Hanayama et al. 2002). Apoptotic cells undergo secondary necrosis leading to the release of damage associated molecular pattern (DAMP) molecules which promote inflammation and tissue injury (Miksa et al. 2006). Promotion of apoptotic clearance has been shown to be beneficial in various brain disease. MFG-E8 levels are reduced in Alzheimer's disease, and decreased MFG-E8 mediated clearance of apoptotic neurons and amyloid β-peptides have been shown to play pathogenetic roles in Alzheimer's disease (Boddaert et al. 2007). The macrophage scavenger receptor A (CD204), which acts similar to MFG-E8 promoting macrophage clearance of apoptotic cells, has been shown to be neuroprotective in focal cerebral ischemia (Lu et al. 2010). However, the effects of MFG-E8 on cerebral ischemia have not been previously investigated. This study has established for the first time a beneficial role of MFG-E8 in focal cerebral ischemia, attributable, at least in part, to suppression of inflammation and apoptosis.
Cerebral ischemia downregulated cerebral MFG-E8 expression at 24 hours after onset of ischemia. Intravenous administration of exogenous rhMFG-E8 one hour after the ischemia reduced infarct size and improved neurological function. Histopathological examination also showed that rhMFG-E8 treatment protected neurons in the penumbra against necrosis. Inflammation (Schilling et al. 2003) and apoptosis (Broughton et al. 2009) play crucial roles in tissue damage during cerebral ischemia. The anti-inflammatory effects of rhMFG-E8 treatment in cerebral ischemia included suppression of cytokine (IL-6 and TNF-α) release, ICAM-1 expression, and cerebral neutrophil infiltration. Upregulation of the ligand-inducible transcription factor, PPAR-γ, may be responsible for the inhibition of cytokine release following treatment with rhMFG-E8. Focal cerebral ischemia by MCAO suppressed PPAR-γ levels. Treatment with rhMFG-E8 attenuated the ischemia-induced downregulation of PPAR-γ compared with vehicle. PPAR-γ is known to suppress NF-κB mediated cytokine production through a variety of mechanisms collectively termed transrepression (Ricote and Glass 2007). PPAR-γ agonists such as the thiazolidinediones have shown neuroprotection in cerebral ischemia (Wang et al. 2009). The finding that rhMFG-E8 mediated upregulation of PPAR-γ together with suppression of cytokine release is consistent with the work of Zhang et al who showed that the PPAR-γ agonist, pioglitazone, suppresses NF-κB signaling in permanent focal cerebral ischemia, resulting in neuroprotection (Zhang et al. 2011).
rhMFG-E8 treatment was also demonstrated to inhibit apoptosis in cerebral ischemia, rhMFG-E8 treatment decreased TUNEL staining in the penumbra and also increased Bcl-2/Bax ratio. Upregulation of the Bcl-2/Bax ratio may be an integrinmediated effect of rhMFG-E8 treatment. The MFG-E8 receptor, αvβ3, has been shown to increase Bcl-2 transcription through a focal adhesion kinase (FAK)-dependent activation of the PI3K-Akt pathway (Matter and Ruoslahti 2001). The anti-apoptotic effect of rhMFG-E8 may further be explained by the upregulation of PPAR-γ. Wu et al showed that PPAR-γ overexpression inhibited apoptosis in cerebral ischemia. Knockdown of PPAR-γ using small interfering RNA abrogated the anti-apoptotic effects of PPAR-γ (Wu et al. 2009a).
The CX3X chemokine, fractalkine, stimulates the release of MFG-E8 from microglial cells (Leonardi-Essmann et al. 2005). The neuroprotective effects of MFG-E8 under conditions of hypoxia/ischemia are further supported by in vitro studies by other investigators using fractalkine. Noda et al showed that fractalkine decreased excitotoxicity by stimulating microglial clearance of apoptotic neurons. Treatment of the microglial cells with anti-MFG-E8 neutralizing antibodies abolished the microglial clearance of necrotic neurons and diminished the neuroprotection (Noda et al. 2011). Similarly, Kranich et al also showed that MFG-E8 protects against neurotoxicity in a model of prion disease (Kranich et al. 2010).
In summary, this first assessment of the role of rhMFG-E8 in cerebral ischemia has shown that rhMFG-E8 suppresses inflammation and apoptosis in a permanent focal cerebral ischemia model and that rhMFG-E8 is a novel neuroprotective agent for cerebral ischemia.
This application claims the benefit of PCT Application No. PCT/US2012/35362, filed Apr. 27, 2012, which claims the benefit of U.S. Provisional Patent Application No. 61/480,031, filed Apr. 28, 2011, the content of which is herein incorporated by reference in its entirety.
This invention was made with government support under grant number GM057468 awarded by the National Institutes of Health. The government has certain rights in the invention.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/US2012/035362 | 4/27/2012 | WO | 00 | 12/17/2013 |
| Number | Date | Country | |
|---|---|---|---|
| 61480031 | Apr 2011 | US |
