Patent Application
20050118145
The present invention relates to the use of Sertoli cells and myoid cells for creating an immunologically privileged site in a mammalian subject, thereby facilitating the transplantation of cells that produce a biological factor in the treatment of a disease that results from a deficiency of such biological factor. Pharmaceutical compositions containing Sertoli cells and myoid cells, as well as therapeutic methods relating to the use of these cells are provided by the present invention.
The testis, brain, and anterior chamber of the eye are considered immunoprivileged sites and have been investigated for their ability to protect cellular grafts [1-3]. Allogeneic and concordant xenogeneic tissues transplanted into the testis survive long term [4-10].
Moreover, parathyroid allografts in the testis restore normocalcemia in parathyroidectomized rats [8] and islets transplanted into the intra-abdominally placed testis correct hyperglycemia in diabetic rodents [9, 10]. Immune tolerance in the testis is due at least in part to Sertoli cells; because grafts are still protected after the selective destruction of the other major components of the testis, Leydig cells and germ cells [11, 12]. Furthermore, rodent Sertoli cells can survive as allografts [13, 14] and allogeneic islets or xenogeneic adrenal chromaffin cells are protected from immune-mediated rejection when co-transplanted with Sertoli cells [14-16]. Sertoli cells comprise a major component of the mammalian testis and are considered “nurse” cells because they provide numerous factors required for the orderly development and protection of spermatozoa [17]. As the germ cells mature they develop surface antigens which are recognized as foreign by the immune system making it necessary for the testis to develop a mechanism for protecting the developing germinal cells [18, 19]. It is believed that Sertoli cells protect the germ cells by creation of the blood-testis barrier [20, 21] and secretion of factors that may lead to local immune tolerance [13, 22-26]. Sertoli cells are known to produce Fas ligand (FasL) [13], transforming growth factor b (TGF β) [27], and clusterin [28], which are believed to have immunoprotective [13, 29], anti-inflammatory [30, 31], and tolerogenic properties [28, 32], respectively. It is postulated that these proteins may be responsible for the immunoprotective ability of Sertoli cells. Further study of these factors in an established model of Sertoli cell transplantation may provide clues to factors necessary for creating a local tolerogenic environment.
Recently, it has been shown that an immunoprivileged site can be created by preengrafting Sertoli cells, which site subsequently protected allogeneic islets from rejection [56]. Long-term survival of porcine islets placed in the repositioned intra-abdominal testis was reported in non-immunosuppressed beagle dogs [57]. Survival of syngeneic rat islet grafts transplanted in the omental pouch was also reported [58]. A model for studying islet development and xenotransplantation has been described [59]. Recent reports have shown the survival of Sertoli cells from 12-week-old Yorkshire pigs in the rat brain, an immunoprivileged site [33]. However, survival of discordant xenogeneic porcine Sertoli cells has not been demonstrated in a non-immunoprivileged site.
The present inventors have demonstrated a long-term survival of neonatal porcine Sertoli cells (NPSCs) in non-immunosuppressed Lewis rats when transplanted underneath the kidney capsule, a non-immunoprivileged site. The present inventors have surprisingly found that the long-term survival of Sertoli cells depends upon the presence of myoid cells.
Accordingly, one embodiment of the present invention provides a pharmaceutical composition containing Sertoli cells, myoid cells and a pharmaceutically acceptable carrier.
In a preferred embodiment, the ratio of myoid cells versus Sertoli cells in the pharmaceutical composition is at least about 0.5:99.5. Preferably, the ratio is in the range of 0.5:99.5 to 65:35.
Sertoli cells and myoid cells each can be isolated from the testis of a mammal, preferably a pig, and more preferably a neonatal pig of 60 days old or younger, and even more preferably, a neonatal pig of 5 days old or younger. Alternatively, Sertoli cells can be obtained from a cell line, which can be either an established cell line such as TM4, or a stem cell line that could be derived from human tissue.
The pharmaceutical composition of the present invention can also include cells that produce a biological factor. In a preferred embodiment, cells that produce a biological factor are cells of pancreatic islets. As to the relative amount of Sertoli cells versus cells of pancreatic islets in the pharmaceutical composition, it is preferred that not more than 2×106 Sertoli cells, i.e., 2×106 or fewer Sertoli cells, are used per 800 islets.
In another preferred embodiment, the pharmaceutical composition is provided in a device suitable for implantation into a mammalian subject.
In another embodiment, the present invention provides a method of creating an immunologically privileged site in a mammalian subject, preferably a human subject, by administering Sertoli-cells and myoid cells into the subject.
In a preferred embodiment, the ratio of myoid cells versus Sertoli cells administered to the subject is at least about 0.5:99.5. Preferably, the ratio is in the range of 0.5:99.5 to 65:35.
Sertoli cells and myoid cells used in the administration can each be isolated from the testis of a mammal, preferably, a pig, and more preferably, a neonatal pig of 60 days old or younger, and even more preferably, a neonatal pig of 5 days old or younger. Alternatively, Sertoli cells used in the administration can be obtained from a Sertoli cell line, either an established cell line such as TM4, or a stem cell line that could be derived from human tissue. Such Sertoli cells prepared from a cell line can be admixed with myoid cells for administration to a subject.
Preferably, Sertoli cells and myoid cells are co-cultured prior to administration under conditions, e.g., for a period of about 24-48 hours, to form Sertoli-myoid cell aggregates.
Sertoli-cells and myoid cells can be administered subcutaneously into a site in the subject or administered intramuscularly. Preferably, the site is selected from the brain, the renal subcapsular space, the liver subcapsular space, the hepatic portal vein, the omental pouch, or the subcutaneous fascia.
According to the present invention, the total amount of Sertoli-cells and myoid cells administered is in the range of 105 to 108 cells. Generally speaking, the amount of cells required to create an immunologically privileged site in a human subject is more than the amount required in a mouse, for example. For administration to a human subject, the total amount of cells administered is preferably about 107 to 108 cells.
The administration can be achieved by implantation of a device encapsulating the cells, or by transplantation. The transplantation can be either allograft or xenograft.
In still another embodiment, the present invention provides a method of treating a disease that results from a deficiency of a biological factor in a mammalian subject, preferably a human, by administering Sertoli cells, myoid cells and a therapeutically effective amount of cells that produce said biological factor to the subject.
Preferably, the ratio of myoid cells versus Sertoli cells administered to the subject is at least about 0.5:99.5 and is in the range of 0.5:99.5 to 65:35.
Sertoli cells and myoid cells administered to the subject are preferably isolated from the testis of a mammal, preferably, a pig, and more preferably, a neonatal pig of 60 days old or younger, and even more preferably, a neonatal pig of 5 days old or younger. Alternatively, Sertoli cells can be obtained from a Sertoli cell line, either an established cell line such as TM4, or a stem cell line that could be derived from human tissue. Such Sertoli cells prepared from a cell line can be admixed with myoid cells and the cells that produce the desired biological factor.
In a preferred embodiment, the biological factor is a hormone.
In another preferred embodiment, the disease is diabetes mellitus and the cells that produce a biological factor are cells of pancreatic islets. It is preferred that the ratio of Sertoli cells versus cells of pancreatic islets is such that not more than 2×106 Sertoli cells are used per 800 islets. It is also preferred that prior to administration of the cells to a subject, Sertoli cells, myoid cells and islet cells are co-cultured under conditions, e.g., for a period of about 24-48 hours, to form Sertoli-myoid-islet cell aggregates for administration.
The cells can be administered subcutaneously into a site in the subject or administered intramuscularly. Preferably, the site is selected from the brain, the renal subcapsular space, the liver subcapsular space, the hepatic portal vein, the omental pouch, or the subcutaneous fascia.
The total amount of Sertoli-cells, myoid cells and cells that produce a biological factor administered to the subject is in the range of 105 to 108 cells. Generally speaking, the amount of cells required to treat a human subject is more than the amount required to treat, e.g., a mouse. For administration to a human subject, the total amount of cells administered is preferably about 107 to 108 cells.
The administration can be achieved by implantation of a device encapsulating the cells, or by transplantation. The transplantation can be either allograft or xenograft.
Materials and Methods
Animals
Male Landrace-Yorkshire neonatal pigs (aged 1 to 3 days) were used as Sertoli cell donors. Male Lewis rats (RT1/1, Charles River Canada, St Constant, Quebec, Canada), aged 8 to 10 weeks, were used as recipients.
Sertoli Cell Isolation
The NPSCs were isolated using a technique similar to that previously described for rat Sertoli cells [14]. Briefly, 1 to 3-day old-male Landrace-Yorkshire neonatal pigs were anesthetized with Halothane, testicles were surgically removed and placed in 50-ml conical tubes containing cold (4° C.) Hank's balanced salt solution (HBSS) supplemented with 0.25% (w/v) bovine serum albumin (fraction V; Sigma Chemical Co., St Louis, Mo., USA). The testes were cut into 1-mm fragments with scissors, digested for 10 min at 37° C. with collagenase (2.5 mg/ml; Sigma Type V, St Louis, Mo., USA) and then washed three times with HBSS. The tissue was resuspended in calcium-free medium supplemented with 1 mM EGTA and further digested with trypsin (25 μg/ml; Boehringer Mannheim, Laval, Canada) and DNase (4 μg/ml, Boehringer) for 10 min at 37° C. The digest was passed through a 500-μm nylon mesh, washed with HBSS and cultured in non-treated Petri dishes (15 cm diameter) containing 60 to 80×106 cells and 35 ml of Ham's F10 media supplemented with 10 mmol/l D-glucose, 2 mmol/l 1-glutamine, 50 μmol/l isobutylmethylxanthine, 0.5% bovine serum albumin, 10 mmol/l nicotinamide, 100 U/ml penicillin, 100 μg/ml streptomycin, and 10% heat-inactivated neonatal porcine serum. Cells were incubated for 48 h at 37° C. to allow the formation of cellular aggregates (100 to 300 μm diameter).
Characterization and Transplantation of Sertoli Cell Grafts
After culture and immediately prior to transplantation, the purity, viability and mass of NPSCs was determined on the basis of the proportion of vimentin-positive Sertoli cells, smooth muscle alpha actin-positive peritubular myoid cells, trypan blue dye exclusion and DNA content, respectively. As it is difficult to accurately count cells in a three-dimensional structure, we assessed the number of vimentin-positive Sertoli cells and smooth muscle alpha actin-positive peritubular myoid cells in representative aliquots after dissociation of the aggregates into single cells using techniques previously described for islet dissociation [34]. The dispersed cell suspension was allowed to attach to Histobond adhesive microscope slides (F.G.R. Steinmetz Inc., Surry, BC, Canada), fixed with Bouin's solution for 30 min, washed with 70% ethanol and immunostained using the Sertoli cell marker, vimentin [14] or the myoid cell marker, smooth muscle alpha actin [35]. In each preparation a minimum of 500 single cells were counted.
Cell viability was measured at the time of transplantation using a trypan blue dye exclusion assay. This assay is based on the principle that viable cells do not take up trypan blue dye while non-viable cells will take up the dye. Cellular aggregates were dissociated as described previously [34] and incubated with 0.1% trypan blue dye (Sigma) for 5 min. Stained and nonstained cells were counted and the percentage of viable cells calculated.
To assess cell recovery after culture and standardize the mass of NPSCs transplanted in each experiment, three representative aliquots of the cellular aggregates were measured for total cellular DNA content using a Hoefer DyNa Quant 200 fluormetric assay (Amersham Pharmacia Biotech, San Francisco, Calif., USA). Aliquots were washed with citrate buffer [150 mmol/l NaCl, 15 mmol/l citrate, 3 mmol/l ethylene diamine tetraacetic acid (EDTA), pH 7.4], resuspended in TNE buffer (10 mM Tris, 0.2 mM NaCl, 1 mM EDTA, pH 7.4) and solicited. Aliquots of 10 ll were assayed in triplicate by diluting them in 2 ml of assay solution (0.1 μg/ml Hoechst 33258 in 1×TNE) and measuring fluorescence (365 nm excitation/460 nm emission). Samples were run in parallel with and diluted in proportion to a six-point (0-500 ng/ml) DNA standard curve generated using calf thymus DNA. When considering the mean DNA recovery in each preparation, with the DNA content of porcine Sertoli cells (6.6 pg DNA/cell), the total number of cells was subsequently calculated. For transplantation, aliquots consisting of 11×106 cells were placed in polypropylene microcentrifuge tubes, aspirated into polyethylene tubing (PE-50), pelleted by centrifugation, and gently placed under the left renal subcapsular space of Halothane-anesthetized Lewis rats [14].
Assessment of NPSC Survival Post-Transplantation
Histology
Nephrectomies were performed for morphological analysis at 4 (n=3), 20 (n=5), 30 (n=8), 40 (n=5), 60 (n=10) and 90 (n=3) days posttransplant. The graft-bearing kidneys were immersed in Z-fix and embedded in paraffin. After deparaffinization and rehydration, tissue sections were immunostained using antigen retrieval by heating for 15 min in 0.01 M sodium citrate buffer (pH 6.0), in a microwave at full power [14, 36, 37]. Consecutive sections were incubated with 10% hydrogen peroxide to quench endogenous peroxidases, blocked with non-specific serum, and incubated with either mouse monoclonal antivimentin (PCNA; 1:100; Dako, Carpinteria, Calif., USA), or mouse monoclonal anti-proliferating cell nuclear antigen (1:50; Dako) for 30 min. Sections were then incubated with biotinylated goat anti-mouse secondary antibody (1:200; Vector Laboratories, Burlingame, Calif., USA) for 20 min followed by peroxidase-streptavidin, substratechromagen (aminoethyl carbazole) and then stained with hematoxylin (Zymed Laboratories Inc., San Francisco, Calif., USA). Positive controls included sections of neonatal pig testes, whereas negative controls included omission of primary antibody. Positive controls demonstrated vimentin and PCNA immunoreactivity within Sertoli cells and negative controls had no staining.
DNA Extraction, PCR and Sequence Analysis
Nephrectomies were also performed for DNA extraction, under sterile conditions to prevent cross contamination, at 4, 20, 30, 40, 60, and 90 days post-transplant (n>3/timepoint). Tissue from grafts and non-graft-bearing kidneys were immediately frozen and stored at −80° C. for later DNA isolation. After thawing on ice, samples were resuspended in 350 μl of lysis buffer [50 mM Tris, 100 mM EDTA, 400 mM NaCl, 0.5% sodium dodecyl sulfate (SDS)] and treated with 0.2 mg/ml proteinase K (Sigma) overnight at 55° C. Following proteinase K inactivation, chloroform extraction and ethanol precipitation, DNA pellets were washed in 70% ethanol, air dried and dissolved in 100 μl of DNase/RNase free water (Sigma). DNA concentration and quality were determined by spectrophotometric analysis prior to amplification.
To confirm the presence of porcine DNA, primers specific to the porcine mitochondrial gene encoding COII [38] and to the housekeeping gene, mouse glyceraldehyde-3-phosphate dehydrogenase (GAPDH) were used. The COII PCR was two stage (nested) while GAPDH was single stage. The starting template in the first amplification of the nested and single stage PCR was 0.5 to 1 μg of DNA in a 50-μl volume containing 1×PCR buffer, 2 mM MgCl2, 300 nM of each primer, 200 μM dNTP and 1.5 U Taq DNA Polymerase (Invitrogen Carlsbad, Calif., USA). In the nested PCR, 2 to 3% of the first reaction served as the template in the second round of amplification. All amplifications were performed using the Gene Amp PCR System 9700 (Applied Biosystems, Foster City, Calif., USA) with the following cycling conditions:94° C. 3-min denaturation followed by either 25 cycles (first PCR) or 30 cycles (second PCR) of 94° C. for 30 s, 56° C. for 30 s, 72° C. for 30 s, and final extension of 72° C. for 10 min. PCR products were electrophoresed through an ethidium bromide stained agarose gel (1.5%) and photographed. COII PCR products of the expected size were ligated into the pCR4-TOPO vector (TOPO TA Cloning Kit for Sequencing, Invitrogen) and sequenced. Unknown sequences were analyzed using BLAST (NCBI) and compared with known GenBank sequences. The sequenced band was identical to the region of porcine COII DNA from 7112 to 7426 bp (GENBANK accession number AF304202) verifying the specificity of the PCR product. Primers for COII were:first PCR FORGCT TAC CCT TTC CAA CTA GGC TTC and REV- TTC GAA GTA CTT TAA TGG GAC AAG, second PCR FOR- CAC ACA CTA GCA CAA TGG ATG CC and REV- GAG GAT ACT AAT ATT CGG ATT GTT AT. Primers for GAPDH were:FOR- AAT CCC ATC ACC ATC TTC CA and REV- GGC AGT GAT GGC ATG GAC TG.
Results
NPSC Aggregate Characterization
Porcine Sertoli cells were isolated from neonatal testes and cultured for 2 days to allow for formation of cellular aggregates. Prior to transplantation, the composition of these cellular aggregates was determined by assessing the proportion of immunoreactive vimentin-positive Sertoli cells and smooth muscle alpha actin positive myoid cells [14, 35]. From a total of four independent preparations, these aggregates were shown to contain 92.2±5.1% Sertoli cells and 2.2±0.7% myoid cells. The remaining cell population (i.e. <6%) is likely composed of germ cells, Leydig cells and fibroblasts.
On the basis of the total DNA content of each NPSC preparation and the observation that single NPSCs contain 6.6 pg DNA/cell (data not shown), it was calculated that 52.5±13.3×106 cells were obtained per testis and each implant contained 11×106 cells. In view of the percentage of vimentin-positive Sertoli cells, the number of Sertoli cells within each graft should therefore be approximately 10.1×106. In addition, the cell viability was measured by trypan blue dye exclusion and the cellular preparation at the time of transplantation was shown to consist of 98.6±1.7% viable cells.
Survival of Porcine Sertoli Cells
The NPSCs were implanted under the kidney capsule of immunocompetent Lewis rats to ascertain whether they could survive as discordant xenografts. Macroscopically at 4, 20, 30, 40, 60 and 90 days post-transplant, Sertoli cell grafts were easily identifiable with extensive neovascularization (
To further confirm the survival of Sertoli cells in the xenografts, PCR for a porcine-specific gene was performed. After 4, 20, 30, 40, 60 and 90 days posttransplant grafts were removed and the DNA extracted for porcine mitochondrial COII PCR. COII is a marker for porcine tissue [38] and was used in the present study to confirm the presence of NPSCs in the recipients. Negative controls consisting of rat tissue from the untransplanted kidney were performed for each graft to verify the specificity of the primers for porcine DNA. No positive signal was detected in the non-transplanted kidneys (
aGrafts were used for both immunostaining and PCR.
Macroscopically, extensive growth of the Sertoli cell grafts was observed at 20 days post-transplant. Due to the apparent growth of the grafts as well as the potential for unregulated proliferation of the grafted cells, tissue sections were immunostained for PCNA to identify dividing cells. PCNA is involved in DNA replication and is localized to proliferating cells [40-42]. When consecutive sections were immunostained for vimentin (
Discussion
Our results indicate that NPSCs survive long term following xenogeneic transplantation in non-immunosuppressed Lewis rats. Survival was determined histologically by vimentin immunostaining and further verified by COII PCR. Although other studies have reported survival of discordant [pig-to-rat; 33] and concordant [rat-to mouse; 43] Sertoli cells transplanted in rodents, these grafts were either implanted in the brain [33] which is considered an immunoprivileged site [3], or they were placed in an immunoprotective alginate microcapsule [43]. To our knowledge, the present study is the first to report survival of a discordant xenograft without using immunosuppression or any other immune-modulating intervention. The ability of NPSCs to survive in xenogeneic recipients indicates that they likely synthesize and secrete immune-modulating factor(s) that prevent their rejection. Further study of these factors may provide a model to examine the immunology of tolerance. For example, Sertoli cells are known to produce FasL [13], TGF β [27] and clusterin [28] which are all suggested to play a role in graft protection. Sertoli cells also secrete unidentified factors that decrease IL-2 production [24] and T cell proliferation [24-26]. Previous data indicate that FasL secreted by Sertoli cells may play a role in the survival of mouse testicular tissue fragments transplanted under the kidney capsule of allogeneic recipients [13]. In particular, testicular tissue isolated from grid mice (lacking functional FasL) transplanted as allografts were no longer present after 7 days while grafts from wild type mice (producing functional FasL) survived for 28 days [13]. However, more recent papers suggest that the immunoprotective effect Sertoli cells exhibited when co-transplanted with non-obese diabetic (NOD) mouse islets in diabetic NOD mice is not associated with FasL [22, 23], but that FasL is rather detrimental and correlates with neutrophil recruitment and subsequent graft destruction [22]. On the other hand, our previous study using the NOD mouse Sertoli cell/islet co-transplant model indicates that TGF β plays a protective role in preventing islet destruction [23].
It is likely that a combination of immunomodulating factors, as opposed to a single protein produced by NPSCs, permits their survival in xenogeneic recipients. One example is a report by Chen et al. [44] demonstrating that a colon carcinoma cell line transfected to express FasL and injected subcutaneously was rapidly rejected by neutrophil recruitment and activation [44]. However, when these cells were engineered to express both FasL and TGF β the grafts survived [44]. The authors suggest the combined protection is most likely due to the inhibition of p38 mitogen-activated protein kinase (MAPK) function by TGF β preventing the FasL-induced neutrophil cytotoxicity that is dependent on p38 MAPK [44]. Thus, TGF β and FasL may act synergistically to promote NPSC survival by reducing inflammation and increasing clonal deletion of lymphocytes. Clusterin, an amphipathic glycoprotein and one of the most abundant proteins secreted by Sertoli cells, is also known to have many immune-modulating functions. In particular, clusterin has been shown to:exhibit anti-inflammatory properties [28], be up-regulated and provide a local protective effect for undamaged cells after cell injury or death [28], play a role in tolerance induction for rat liver allografts [45], and inhibit activation of the complement cascade [28, 32]. As hyperacute rejection of discordant xenografts requires activation of the complement system [46], preventing this destructive process would clearly be an important mechanism to prevent rejection. It is therefore possible that TGF β and clusterin, and potentially FasL, are some of the factors secreted by NPSCs that allow them to survive xenogeneic transplantation. Further study of the mechanism for xenogeneic survival of porcine Sertoli cells may provide information on the induction of tolerance and inhibition of complement activation.
The survival of xenogeneic porcine Sertoli cells also has potential clinical applications in co-transplantation of cellular grafts for genetic engineering. The recent success of clinical islet transplantation using immunosuppressive therapy [47] provides the basis for further islet transplantation in humans. In order for this approach to become a reality for young juvenile type 1 diabetic patients, the immunosuppressive regimen would have to be replaced with an alternative strategy. Due to the ability of Sertoli cells to immunoprotect allogeneic [14,15] and NOD mouse [22, 23] islet grafts in rodents, the creation of an immunoprivileged site with Sertoli cells may be a solution. However, humans are not a practical source of Sertoli cells due to the lack of available human donor tissue and data in a recent paper indicating the inability of human testicular cells to survive transplantation in mice [48]. Pigs are relatively abundant and we have shown that NPSCs are easily isolated and survive as xenografts in rodents. This implies that pigs are an ideal source of Sertoli cells for creation of an immunoprivileged site for islets. In addition to islet grafts, creation of an immunoprivileged ectopic site with NPSCs may also be useful for cellular grafts such as neuronal cells [16, 33]. Otherwise, Sertoli cells could be engineered to produce therapeutic proteins such as dopamine or factor VIII to potentially treat diseases such as Parkinsonism or hemophilia.
Prior to the use of porcine Sertoli cells in a clinical situation the potential for tumor formation must be addressed. Therefore, we examined the proliferation of the NPSCs after transplantation into Lewis rats by immunostaining for PCNA and found little if any proliferation in the long-term grafts. Many PCNA-positive cells were detected at 20 days, however, this number decreased by 40 days and almost no positive cells were present at 60 and 90 days. Sertoli cells in the native testis have been shown to proliferate during post-natal testicular development until puberty at which time they cease to divide [49-51 ]. This growth is regulated by many factors including follicle-stimulating hormone, epidermal growth factor, nerve growth factor, neurotropin-3, and transforming growth factor-a [52-55]. Most likely the Sertoli cells at the time of transplantation to 20 days are relatively immature and so proliferate. As the time post-transplant increases the Sertoli cells likely mature and therefore the number of dividing cells decreases. This suggests that cell division of the transplanted Sertoli cells may be controlled, thereby decreasing the chances of forming tumors.
In conclusion, we have demonstrated long-term survival of xenogeneic NPSCs in rodents without immunosuppression. The survival was verified by mmunohistochemistry and PCR which suggests that Sertoli cells cannot only survive as allografts but also as discordant xenografts. Further study of this model may provide clues to the mechanism of xenograft survival and immune tolerance.
Sertoli cells are normal constituents of the testes where they nurse and immunologically protect the developing germ cells. Isolated Sertoli cells can ectopically create an immunoprivileged site enabling the survival of co-transplanted allogeneic or xenogeneic cells by secreting potent immunosuppressive and survival-enhancing molecules. By harnessing the natural functions of Sertoli cells it may be possible to overcome the major limitations associated with cell transplantation:the shortage of suitable donor tissue and the need for life-long immunosuppression. In pre-clinical animal models, isolated Sertoli cells (1) engraft and self-protect when transplanted into allogeneic and xenogeneic environments, (2) protect co-grafted allogeneic and xenogeneic cells from immune destruction, and (3) enable long term survival of islet co-grafts and reversal of hyperglycemia in animals with diabetes due to pancreatectomy or to autoimmune disease (non obese diabetic model).
Recent efforts to more fully characterize the cellular composition of the Sertoli cell-enriched grafts prior to transplant have revealed that a percentage of myoid cells are also contained within the preparation of successful Sertoli cell transplants. This observation is important because it suggests that the inclusion of myoid cells might play an important role in optimizing the grafts ability to confer the local immunoprotection seen in transplant studies performed by STI. There are several lines of evidence suggesting that myoid cells and Sertoli cells do indeed interact in several important ways. First, in the native testes, myoid cells are found in close proximity to Sertoli cells where they form part of the basement of the seminiferous tubule and provide a major role in the movement of intratubular fluid and the propulsion of released spermatozoa. Secondly, myoid cells play a role in regulating the function and activity of Sertoli cells by producing factors (such as PmodS) that modulate the cytodifferentiation and function of the Sertoli cell. Finally, myoid cells themselves produce growth factors and cytokines such as TGF that are believed to be immunoprotective and could add to the already potent cocktail of growth factors and cytokines produced by Sertoli cells.
The contribution of myoid cells to the immunoprotection produced by Sertoli cell-enriched transplants can be tested by the experiments as listed below:
(1) Experiments were designed to determine whether xenogeneic neonatal porcine Sertoli cells survive transplantation in rats without the use of immunosuppression. Sertoli cells were isolated, cultured and then transplanted under the kidney capsule of non-immunosuppressed Lewis rats. Using immunocytochemical techniques, the cultured cell preparations were found to contain 92±5.1% Sertoli cells (Vimentin staining) and 2.2±0.7% myoid cells (smooth muscle alpha actin staining). To assess survival, grafts were removed after 4, 20, 30, 40, 60, and 90 days post-transplant and immunostained for the Sertoli cell marker vimentin. Survival was confirmed by PCR for the porcine mitochondrial cytochrome oxidase II subunit gene (COII), a marker for porcine tissue. By both methods, Sertoli cells were detected in the grafts for at least 90 days. Histologically, Sertoli cells were clustered in small aggregates or organized in tubule-like structures. Staining of adjacent sections also revealed that viable myoid cells were present within the Sertoli cell transplant sites (
(2) Histological studies confirm that viable co-grafted Sertoli cells and islet transplants contain abundant surviving myoid cells as well. Eleven million Lewis Sertoli cells and 2000 Lewis islets were transplanted underneath the kidney capsule of diabetic Wistar-Furth rats. The grafts were removed one month later and stained immunocytochernically for Sertoli cells using GATA-4 and myoid cells using smooth muscle alpha actin. Viable Sertoli cells were found throughout the transplant site and frequently re-organized in tubule-like structures. Using adjacent tissue sections it was found that the re-formed tubular structures were lined by abundant viable myoid cells in a manner reminiscent of the native testes (
(3) One additional way of determining the relative contribution of myoid cells to the local immunoprotection described above is to transplant pure Sertoli cells without any myoid cells. Sertoli cell lines, by definition, do not contain myoid cells. By transplanting such a cell line together with islet cells it is possible to gain further insight into the contributory role of other cells including myoid cells in our earlier studies. Toward this end, 500 Balb/c islets were transplanted together with varying numbers of the cell line MSC-1 (a mouse-derived Sertoli cells line) under the kidney capsule of diabetic C3H mice. Histological analysis using T-antigen staining revealed that even though the MSC-1 cells are a tumorigenic cell line they survived poorly and were distributed in small clusters one month after transplantation. Staining of the same or adjacent sections for insulin revealed that the MSC- 1 cells did not protect the co-grafted islets (
The above experiments demonstrate the presence of myoid cells in successful immunomodulating Sertoli cell rich grafts. A percentage of myoid cells between 0.5% and 65% appears to be found in successful grafts. In the next months we will attempt to identify a method to ablate the myoid cells in Sertoli cell rich grafts and to selectively vary the percentage of myoid cells in the Sertoli cell rich transplants to determine if there is a dose effect associated with survival of the graft in a foreign recipient. The Sertoli cell line data suggest that one of the reasons the MSC-1 grafts failed prematurely is the absence of a supporting population of myoid cells. To determine that the premature destruction of the graft is not due to a reduction in the cell's immunomodulating ability caused by the immortalization or proliferation process, in the next months we will attempt to transplant MSC-1 grafts with varying levels of murine myoid cells and evaluate the survival against the current baseline data.
References
This application claims priority from U. S. Provisional Application No. 60/484,960, filed on Jul. 3, 2003.
| Number | Date | Country | |
|---|---|---|---|
| 60484960 | Jul 2003 | US |
