Patent Application
20070003483
The present invention relates to a method of evaluating organ function. More specifically, the present invention relates to a method for analyzing visually and/or for determining quantitatively multiple indices with microanatomical orientation vascular system and/or excretion pathways.
Although use of University of Wisconsin solution has improved mean preservation time for liver transplantation, the incidence of primary graft nonfunction and initial poor function still persist (1-3). The clinical incidence of such a dysfunction and the resultant loss of graft survival depend on the storage time (1-4). Reperfusion injury is the key event leading to the graft failure after prolonged cold ischemia (5-9). During the storage, hepatocytes swell and form blebbing (6-8). Upon reperfusion, however, these changes in the parenchymal cells were restored without leading to their irreversible injury (6-8). On the other hand, sinusoidal endothelial cells lose their viability and Kupffer cells are activated (6-10). According to previous studies using rat liver grafts stored in UW solution, the critical storage time when the changes in sinusoidal cells occur is longer than 16 hrs (6, 7). In these grafts, the cells were damaged to cause platelet trapping (10), fibrin deposition (11), and leukocyte margination (12). In grafts stored for shorter duration, hepatic ATP content was reported to be well recovered after reperfusion, suggesting that parenchymal cells are viable (13, 14).
Apart from these data, it has not been carefully examined if hepatocytes lose their functions without displaying irreversible injury and then interfere with the graft function as a whole. Although biliary output, clearance of taurocholate and bromosulfophtalein were measured in previous studies (13-15), they failed to demonstrate such functional alterations in hepatocytes even when the storage time was extended to 18 hrs (13). Besides these studies, little information has been available as to alterations in the ability of the post-cold ischemic grafts to excrete bile constituents. Such indices include the ability of hepatocytes to yield the osmotic driving force for bile formation, and to excrete bile salts or organic anions; thus, excretion of glutathione and bilirubin could serve as a marker detecting early hepatocellular changes in the grafts. The ability to excrete organic anions could determine the efficiency of the graft to detoxify xenobiotics and the severity of post-cold ischemic hyperbilirubinemia, a risk factor for allograft dysfunction in clinical transplantation (2, 16).
It is an object of the present invention to provide a method of evaluating organ function. Based on the above findings, the present inventor continued further investigations.
In attempt to determine such an ability of post-cold ischemic grafts, we have herein examined changes in constituents of bile samples as a function of the storage time, and revealed impaired excretion of glutathione and bilirubin as an early event on hepatocytes. This event turned out to be the result of cytoplasmic re-localization of multidrug resistance associated protein 2 (Mrp2), an ATP-dependent transporter for biliary excretion of the organic anions. Our results suggest that the function of this transporter is impaired whereas the grafts apparently maintain their overall energy charges without showing any notable hepatocellular damages. Furthermore, mechanisms for such a change in hepatocytes appear to involve thromboxane synthesis in Kupffer cells in grafts exposed to a rather short duration of cold ischemia; i.e. 8 hrs.
The present application provides the following inventions:
(1) A method of analyzing organ or tissue injury, comprising the following steps of:
(2) The method of (1), wherein the organ or tissue is at least one selected from the group consisting of liver, kidney, lung, pancreas and gastrointestinal tracts.
(3) The method of (1) or (2), where the step (b) further comprises a step of obtaining microanatomical orientation of vascular system and/or excretion pathways.
(4) The method of any one of (1) to (3), wherein the analysis is carried out visually and/or quantitatively.
(5) The method of any one of (1) to (4), wherein the cell condition is at least one selected from the group consisting of cell viability, cell injury, molecular transport, and mitochondrial function.
(6) A method of evaluating drug toxicity, comprising the following steps of:
(7) The method of (6), wherein the organ or tissue is at least one selected from the group consisting of liver, kidney, lung, pancreas and gastrointestinal tracts.
(8) The method of (6) or (7), where the step (b) further comprises a step of obtaining microanatomical orientation of vascular system and/or excretion pathways.
(9) The method of any one of (6) to (8), wherein the analysis is carried out visually and/or quantitatively.
(10) The method of any one of claims 6 to 9, wherein the cell condition is at least one selected from the group consisting of cell viability, cell injury, transport of molecules in and around cells, and generation of biologically active compounds, blood flow, and tissue oxygenation.
Hereinbelow, the present invention will be described in more detail.
Although Kupffer cells (KC) have been thought to play a crucial role in post-cold ischemic hepatocellular injury, their roles in non-necrotic graft dysfunction remain unknown. This study aimed to unravel such roles of KC in the post-cold ischemic liver grafts. Rat livers treated with or without liposome-encapsulated dichloromethylene diphosphonate, a KC-depleting reagent, were stored in University of Wisconsin solution at 4° C. for 8-24 hrs and reperfused under monitoring biliary output and constituents. An ability of hepatocytes to excrete bile was assessed through laser-confocal microfluorography in situ. Cold ischemia-reperfused grafts decreased their bile output significantly at 8 hrs without any notable cell injury. This event coincided with impaired excretion of glutathione and bilirubin-IXα, suggesting retarded transport of these organic anions. Mechanisms involved intracellular re-localization of multidrug resistance protein-2 (Mrp2). Kinetic analyses for biliary excretion of carboxyfluorescein, a fluoroprobe excreted through this transporter, revealed significant delay of the dye excretion from hepatocytes into bile canaliculi. The KC-depleting treatment significantly attenuated this decline in biliary anion transport mediated via Mrp2 in the 8-hr cold ischemic grafts through re-distribution of Mrp2 from the cytoplasm to the canalicular membrane. Furthermore, mechanisms appeared to involve thromboxane A2 synthase in KC, since improving effects of blocking this enzyme on CF excretion and on cytoplasmic internalization of Mrp2 disappeared in the KC-depleting grafts. In conclusion, these results suggest that KC activation is an important determinant of non-necrotic hepatocellular dysfunction, jeopardizing homeostasis of the detoxification capacity and organic anion metabolism of the post-cold ischemic grafts.
In the present specification, some abbreviations are used: BC, bile canaliculi; BR-IXα, bilirubin-IXα; CF, 5-carboxyfluorescein; CFDA, 5-carboxyfluorescein diacetate; EHBR, Eisai hyperbilirubinemia rats; GSH, reduced glutathione; KC, Kupffer cells; LDD, liposome-encapsulated dichloromethylene diphosphonate; Mrp2, multidrug resistance protein 2; TXA2, thromboxane A2.
In one embodiment of the present invention, a method of analyzing organ or tissue dysfunction and/or injury is provided. The method comprises the following steps:
(a) labeling the organ or tissue with one or two dyes;
(b) obtaining multiple indices indicating cell and/or organ functions involving molecular transport and excretion, xenobiotic metabolism and/or cell condition of said organ or tissue; and
(c) analyzing the organ or tissue injury from said indices.
In the present invention, organ or tissue injury means necrosis, apoptosis or disruption of cytoplasmic membrane.
In order to label the organ or tissue under living conditions, conventional methods using a dye (e.g. fluorescent dye, rhodamines or fluorescein salts or propidium iodide) may be employed. For example, these dyes may be loaded with intravenous injection or intraperitoneal injuection in experimental animals, or with intravascular perfusion with their controlled concentrations into the isolated perfused organ preparations in liver, kidney, pancreas, gastrointestinal tracts or lung.
Multiple indices means cell viability, mitochondrial membrane potentials, oxygen free radicals, transport of anions or cations across the cell membrane, cytoplasmic membrane potential, and cell death including apoptosis or necrosis. Examples of the mutiple indices include, but are not limited to xenobiotic metabolism and cell viability.
Xenobiotic metabolism means metabolism and/or catabolism of any types of exogenous reagents or medicines that are degraded in the body.
Cell condition means any types of functional states of living cells including molecular transport (e.g. molecular transport in and aroudnd cells), membrane potential, mitochondrial function, generation of biologically active compounds (generation of bioactive species), blood flow and tissue oxygenation, and uptake and excretion of anions and cations, and those of cells losing their viability such as necrosis or apoptosis. Examples of cell condition include, but not limited to cell viability and cell injury.
In one embodiment of the present invention, a term “microanatomical orientation” means geographic relationship between cells and their surrounding structures such as microvascular systems and the interstitial space involving lymphatic systems and/or connective tissues (e.g. bile canalicular system in the liver). Thus, examples of the microanatomical orientation include, but not limited to bile canalicular networks in liver.
A term “vascular system” means macro and microcirculatory systems involving conducting vessels, arterioles, capillaries and venules.
A term “excretion pathway” means pathways that allow intracellular molecules to be excreted into the extracellular space.
In the present invention, a monitoring of whole-organ functional parameters may be employed to investigate organ or tissue injury visually or quantitatively. A term “visually” means capture of intravital images that include quantitative information of biological activities. A term “quantitatively” means determinating values that indicate biological activities. The whole-organ functional parameters include, but not limited to bile output, determination of bile constituents such as bile acids, phospholipids, cholesterol and bicarbonate.
In another embodiment of the present invention, a method of evaluating drug toxicity is provided. In the present invention, the following steps are included:
In the present invention, a drug toxicity means any types of harmful actions of reagents or medicines on living cells involving inhibition of enzymes or transporter functions. Examples of the drug include, but not limited to inhibitor of ABC transporter (e.g. Probenecid as an inhibitor of mrp2, cyclosporine, adriamycin, cysplatinum, cimetidine, etc.).
A word “applying a test drug” means contacting a drug of interest to organ or tissue. The drug toxicity may be evaluated by analyzing the organ or tissue injury from some indices. For example, when indices for function of any ABC transporter are changed, then it is evaluated that the drug (e.g. ABC transporter) has a toxicity to the organ or tissue. When the indices are kept stable, then it is evaluated that the drug (e.g. ABC transporter) has not a toxicity to the organ or tissue.
The present invention provides evidence that the impaired ability of hepatocytes to execute the Mrp2-dependent excretion of organic anions accounts for an early event indicating the graft dysfunction caused by organ or cell injury such as cold-ischemia followed by the short duration of reperfusion. This change on hepatocytes was subtle and non-necrotic, but critical enough to cause the imbalance between the cellular generation and excretion of glutathione and bilirubin at the level of whole grafts. Extending the duration for cold ischemia up to 16 hrs induced dysfunction of bile canaliculi as characterized by disappearance and dilation of them, while their polygonal networks were kept intact unless the duration of cold storage exceeded 8 hrs. To our knowledge, it remains unknown whether such a non-necrotic dysfunction of hepatocytes exposed to a relatively short period of cold ischemia could be mediated by post-ischemic responses of sinusoidal cells involving KC. As hereby shown, the reduced ability to excrete organic anions via Mrp2 was completely restored by depleting KC, suggesting involvement of this sinusoidal cell in mechanisms for the dysfunction.
The impairment of Mrp2-mediated transport in the 8-hr post cold-ischemic grafts results from cytoplasmic re-localization of this transporter from canalicular membrane but neither from disruption of bile canalicular networks nor from oxidative modification of the transporter by itself; this is consistent with our previous observation that the 8-hr cold ischemia and reperfusion does not show any notable oxidative stress in the liver grafts (14). Alterations in cAMP, a determinant for bile canalicular sorting of Mrp2 (32, 40, 41), are unlikely to play a role in the KC-mediated dysfunction, because its content did not differ irrespective of the presence of KC. Hepatocellular content of ATP are another determinant for the transporter function, but likely to play little role, if any, in the mechanisms, since any differences were notable between the KC-depleting and control grafts having undergone 8-hr cold ischemia. Since the KC depletion did not alter the ability of Mrp2 to excrete organic anions in normal livers, such an alteration of the transporter function in the grafts appears to result from responses of KC that cannot be triggered unless the graft had undergone cold ischemia-reperfusion. Although detailed mechanisms remained unknown, the present results suggest involvement of TXA2 synthase, the enzyme responsible for TXs, a major class of prostanoids released from KC (37, 38). Observation that the preventive effect of the enzyme inhibitor was completely cancelled in the KC-depleted grafts led us to suggest that KC constitutes a major source of TXs that trigger internalization of Mrp2 into the cytoplasm of hepatocytes. Although TXA2 has been thought to exert potent biological actions on various types of cells, previous studies provided evidence that TXB2, a relatively stable metabolite of TXA2, is able to activate non-lysosomal proteinases and thereby triggers bleb formation of primary cultured hepatocytes (42). Thus, further mechanisms by which KC-derived TXs cause hepatocellular function should be necessary.
The newly developed method of the dye exclusion analyses from grafts preloaded with controlled amounts of CF revealed that re-localization of Mrp2 occurs at hepatocellular levels and results in significant deterioration of the whole-graft function. As seen in
In this context, the imbalance between endogenous generation and biliary excretion of BR-IXα in the grafts is of great interest in the current study. As seen in
KC serves as a potent generator of eicosanoids, while hepatocytes and ATP binding cassette transporters expressed on their membrane help their degradation and excretion, respectively (38, 39). On the other hand, anti-oxidant organic anions such as glutathione and bilirubin share Mrp for their excretion into bile in the post-cold ischemic grafts. Thus, the balance between KC-mediated synthesis of eicosanoids and their removal from hepatocytes could determine redistribution of the anti-oxidant anions in and around hepatocytes and thereby dictate functional outcome of liver transplantation. KC-mediated remodeling of Mrp-mediated organic anion transport deserves further studies provided that quantitative information on intra- and inter-cellular kinetics of glutathione, and BR-IXα becomes available to examine if KC-yielded thromboxanes could serve as an early alert mechanism against subsequent oxidative stress on the graft.
Hereinbelow, the present invention will be described in more detail with reference to the following Examples. It should be noted that the technical scope of the present invention is not limited by these Examples.
Materials and Methods
Animal Preparation
The experimental protocols herein described were approved by our institutional guidelines provided by the Animal Care Committee of Keio University School of Medicine. Male Wistar rats (220-260 g, CLEA Japan, Tokyo) and Eisai hyperbilirubinemia rats (EHBR) (220-260 g, Sankyo Inc., Tokyo) that had been allowed free access to laboratory chow and tap water were fasted 24 hrs before experiments. Livers of these rats were perfused ex vivo with the oxygenated Krebs-Henseleit buffer as the base-line perfusate (17, 18), and stored in the University of Wisconsin solution at 4° C. for desired lengths of time (14). When necessary, rats were pretreated with an intravenous injection of liposome-encapsulated dichloromethylene diphosphonate (LDD) at 24 hrs prior to preparation of the ex-vivo liver perfusion for the cold storage according to our previous studies (14, 19). As described previously, this procedure eliminated Kupffer cells almost completely, as judged by immunohistochemistry (20). After the cold storage, the grafts were gently rinsed with a transportal injection of 40 mL of the lactated Ringer solution and perfused with the oxygenated buffer in the presence or absence of sodium taurocholate at 30 μmol/L at a constant flow (32 mL/min) in a single-pass mode (14, 21). For some experiments, either OKY-046, an inhibitor of thromboxane A2 (TXA2) synthase, or indomethacin (IM), an inhibitor of cyclooxygenase, was added in UW solution as well as in the rinse solution at desired concentrations (22).
Determination of Bile and Tissue Constituents
Bile samples were used to determine concentrations of total bile salts, phospholipids, reduced glutathione (GSH) and bilirubin-IXα (BR-IXα) (23, 24). BR-IXα was determined by an enzyme-linked immunosorbent assay using 24G7 (24). This monoclonal antibody can recognize BR-IXα, the terminal heme-degrading product generated specifically through the HO reaction as described earlier (24, 25). Activities of lactate dehydrogenase (LDH) were measured as described earlier (17). Adenosine triphosphate (ATP) in the liver grafts was determined by the luciferrin/luciferase method as described elsewhere (14, 21). Cyclic AMP in the grafts was determined by an enzyme-linked immunosorbent assay (Biotrak™ system, Amersham Biosciences, Buckinghamshire).
Analyses of Biliary Excretion Rates of Carboxyfluorescein
Carboxyfluorescein (CF) is an organic anion which excreted from various cells through Mrp2 (26, 27). The ester precursor of this dye, CF diacetate (CFDA) was loaded transportally into the livers at 50 nmol/L for 10 min in the presence of 1.5 mmol/L probenecid, a potent inhibitor of Mrp2 (26, 28). This reagent can enter hepatocytes and is hydrolyzed by esterase into CF to be excreted into bile (14, 17, 29). After the 10-min CFDA loading, the liver was perfused with the probenecid-free buffer to trigger the excretion of CF into bile. In the cold ischemic groups, the stored grafts were loaded with the CFDA containing buffer for 10 min in the presence of probenecid, and followed by removal of probenecid and subsequent reperfusion for 50 min. Bile samples collected from these preparations were deep-frozen until the fluorescence measurements were carried out using a 96-well multi-channel fluorescence spectrophotometer. The measurements were performed under epi-illumination at 440 nm, the isosbestic wavelength of the dye which yields fluorescence at 510 nm without interference with pH values of the samples (26). The concentration of CF in samples was calibrated with known concentrations of CF dissolved in phosphate buffer saline. As seen later in Results, CF concentrations appeared to decline exponentially with time. With this assumption, biliary CF lifetimes were determined as the T1/2 of the exponential decay. Thus, this method is insensitive to the initial amounts of CF loaded into the perfused liver.
In situ Visualization of Hepatocellular CF Exclusion.
Liver grafts loaded with CF using the aforementioned protocols were observed through intravital laser confocal microfluorography as described previously (14, 20, 30). As shown later in Results, CF was notably loaded into hepatocytes in the presence of probenecid. Upon removal of the reagent, the dye was immediately excluded from hepatocytes, excreted into bile canaliculi (BC) to display honeycomb networks, and finally disappeared from the parenchyma. To examine if the dye exclusion depends on function of Mrp2, some grafts were reperfused with the buffer containing 1.5 mmol/L probenecid. The laser confocal microfluorographs were captured by an inverted-type microscope (Diaphot 300, Nikon/Sankei) equipped with intensified CCD camera (C5810, Hamamatsu Photonics) and multi-pinhole laser confocal processor (CSU-10, Yokogawa Electric Co.). All microfluorographs were digitally processed into 8-bit gray level images. To calibrate the fluorescence intensities, known concentrations of CF were prepared in vitro and the images were captured under the identical optical parameters of the camera. Gray levels in hepatocytes were measured by variable square window (2×2 μm2) using digital image processor (18, 31). At least 10 different hepatocytes in the microscopic fields of interests were analyzed in a single experiment. Assuming that fluorescence intensities measured at the liver surface is identical to those measured in the solution, gray levels were converted to apparent CF concentrations using the calibration line, being designated as CFapp.
We also conducted morphometry to examine structural changes in BC networks as an index of hepatocellular damages. As shown later in Results, normally functioning hepatocytes were characterized by polygonal CF filling in surrounding BC, while those damaged were judged by partial disappearance of the surrounding BC network. The number of such intact hepatocytes surrounded by complete BC filling by CF was counted in the area of interests. Approximately 0.05 mm2 of the liver surface was analyzed in a single experiment for such evaluations.
Immunohistochemical Analyses of Subcellular Mrp2 Distribution
To evaluate Mrp2 in hepatocytes of the grafts, the liver samples were fixed, sliced, and stained with a monoclonal antibody M2III-6, according to previous study (32). The antigen on the sections was visualized by phycoerythrin-conjugated anti-mouse IgG and observed through laser confocal microfluorography at 488 nm as described elsewhere (20, 30). In order to examine BC localization and hepatocellular internalization of Mrp2, the sections were double immunostained with a monoclonal antibody against ZO-1, another marker expressed in hepatocellular junction (33). To determine changes in the protein distribution in a semi-quantitative manner, single-stained microfluorographs of Mrp2 were converted as monochrome 8-bit images (14). The gray levels (1-256) were measured at both cytoplasmic and canalicular domains in a single hepatocytes. At least 5 different sites for each domain were chosen in a single cell to calculate the relative values of cytoplasmic intensities versus the corresponding canalicular intensities. Such a measurement was carried out in 40-60 hepatocytes in 4 different grafts to construct histograms of the percentage cytoplasmic intensities of Mrp2-associated immunoreactivities, being defined as % I-Mrp2(cyt/bc). The elevation of this index represented an increase in the Mtp2 internalization. The histograms were compared among the control grafts and those exposed to cold ischemia with and without the KC-depleting procedure in the presence or absence of the TXA2 synthase inhibitor.
In order to examine differences in Mrp2 expression in the whole liver grafts among the groups, Western blot analyses were carried out using the same monoclonal antibody. We also investigated alterations in oxidative modification of Mrp2 by immunoprecipitating the protein by the antibody M2III-6 to follow Western analyses by an anti-acrolein monoclonal antibody (5F6) (34, 35).
Statistical Analyses
The statistical significance of data among different experimental groups was determined by one-way ANOVA and Fischer's multiple comparison test. P<0.05 was considered significant.
Results
Storage Time-Dependent Reduction of Bile Output in Liver Grafts.
To test the viability of liver grafts, the release of lactate dehydrogenase in the venous perfusate was measured as an index of cell lysis. As seen in Table 1, the grafts exposed to cold ischemia for less than 24 hrs did not display any notable elevation of lactate dehydrogenase.
Data represent means ± SE of measurements (mIU/min/g liver) from the grafts at the onset (0 min) and 60 min after the start of reperfusion (0-24 hrs; n = 5, 48 hrs; n = 3).
*P < 0.05 as compared with the value in other groups.
At 48 hrs, the lactate dehydrogenase release became evident at being and end of the 60 min reperfusion, showing that necrotic cell death was undetectable in cold ischemic grafts exposed to less than 24 hrs under the current experimental conditions.
Alterations in Biliary Excretion of Glutathione and Bilirubin in Post-Cold Ischemic Livers
Observation of a significant decrease in bile flow in the grafts undergoing 16- and 24-hr cold ischemia led us to determine bile constituents responsible for cholestatic changes.
We next examined biliary excretion of GSH under monitoring its tissue content (
Global and Local Assessment of Mrp2 Function by Carboxyfluorescein Exclusion.
Alteration in biliary excretion of GSH and BR-IXα raised a possibility that the ability of Mrp2 to eliminate these organic anions from hepatocytes could be impaired in grafts exposed to prolonged cold ischemia. However, since initial amounts of glutathione and BR-IXα were different among groups, measuring biliary excretion of these endogenous anions did not allow us to make a fair comparison of the organic anion-excreting ability of the grafts. To overcome this difficulty, the grafts were loaded with CF, an exogenous organic anion, and its elimination from hepatocytes into bile was examined. As seen in the left panels of
Careful scanning at the site of bile canaliculi in these microfluorographs captured at 10 min showed minimal but notable changes in structure of the canalicular networks. As seen in
The retardation of the CF exclusion was further examined in a quantitative manner by monitoring temporal alterations in the fluorescence in hepatocytes of the grafts (
Effects of KC Depletion on Biliary CF Excretion in 8-hr Cold Ischemic Grafts.
We then attempted to evaluate the ability of the 8-hr cold ischemic grafts as a whole to excrete CF. To this end, the T1/2 values for the dye exclusion were determined (
To reveal mechanisms by which KC in the 8-hr cold ischemic grafts caused prolonged CF excretion through mrp2, we examined involvement of thromboxanes, a major prostanoid released from activated KCs under post-cold-ischemic conditions (37, 38). To this end, effects of OKY-046, an inhibitor of TXA2 synthase, were examined. As seen in
Intracellular Re-Localization of Mrp2 by 8-hr Cold Ischemia and its Attenuation by KC Depletion.
Since KC is known to down-regulate Mrp2 in endotoxin-treated livers (39), we examined if such a change could be involved in the mechanisms for the dysfunction of the transporter. As shown by Western blot analyses, amounts of Mrp2 protein was unchanged in the 8-hr cold ischemic grafts (
We determined differences in hepatic contents of ATP and cAMP in the KC(+) and KC(−) grafts after the 8-hr cold ischemia-reperfusion, but without any notable significance between the two groups (3.4±0.9 vs 2.9±1.1 μmol/g liver in ATP content, and 8.9±1.0 vs 9.2±0.5 pmol/g liver in cAMP content, respectively). These results suggest that amelioration of intracellular retrieval of this ATP-binding protein by the KC depletion did not result from alterations in tissue contents of ATP and cAMP.
The present invention is useful for a revival of preclinical reagents that were previously dropped off for its organ toxicity. Overall, detailed mechanisms for the toxicity of compounds indicating hepatotoxicity upon routine clinical chemistry remain largely unknown. If such compounds are examined in detail through the present intervension and turn out to block only transporter function without affecting cell viability, minor modification of the chemical structure would be effective to be applied for clinical use. (2) Application of the present method to immunodeficient mice implanted with human cancer cells allows us to examine specificity of any types of drug delivery and accumulation to tumor cell aggregates in vivo or to intact tissues. Such an application is extremely useful to examine the delivery and elimination of anti-cancer reagents in in-vivo implanted cancers, since function of transporters such as mrp2 is an important determinant of the drug resistance of tumors. Application of preclinical experiments for screening potentials of anti-cancer and anti-thrombotic reagents.
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All documents are hereby incorporated by reference for all purposes.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP04/14566 | 9/28/2004 | WO | 3/21/2006 |
| Number | Date | Country | |
|---|---|---|---|
| 60506506 | Sep 2003 | US |
