Effect of Mesenchymal Stem Cells Associated to Matrixen on the Erectile Function in the Rat Model with Bilateral Cavernous Nerve Crushing Injury

ARTICLE INFO _______________________________________________________________________________ IBJU | MESENCHYMAL STEM CELLS ASSOCIATED TO MATRIXEN ON THE ERECTILE FUNCTION AFTER CAVERNOUS NERVE CRUSHING INJURY 834 tients submitted to radical prostatectomy and it is an important reason for the decrease of the quality of life in these patients. Therefore, nerve-sparing procedures have been proposed to reduce short-term and long-term functional complications such as erectile dysfunction (3-5). However, some patients submitted to radical prostatectomy with nerve-sparing technique have been experiencing erectile dysfunction and need other treatments to improve their symptoms (6). Mesenchymal derived stem cells (MSCs) from bone marrow seems to be one of the attractive treatments for tissue regeneration and engineering due to their differentiation potentials into various adult tissues, including endothelial cell, smooth muscle and nerve (7). Therefore, there have been several studies using MSCs and the treatment effect of MSCs has been studied in the animal model of erectile dysfunction caused by cavernous nerve injury. As a result, stem cell therapy may be one of the treatment options for the patients that lost their potency after radical prostatectomy. However, some diffi culties appeared in stem cell therapy in spite of their therapeutic effect. For example, stem cells were easily spread-out to the adjacent tissue after stem cell injection into the target tissue according to the report by Lee et al. (8). This may cause unexpected, unfavorable events and moreover, we are not able to get anticipating results from the stem cell therapy, neither. To overcome this weakness, some investigators used polymers to promote the retention of stem cells in the targeted tissue (9-11). Among various biomaterials, Matrixen is a collagen based biocompatible polymer and it has been used widely as scaffolds in medical fi eld. In addition, Matrixen is easy to handle depending on the investigator’s purpose due to its characteristics of thermo-dependant sol-to-gel transition. Therefore, we used Matrixen to enhance the implantation ability of MSCs and compared the effect of MSCs and MSCs mixed with Matrixen in rats with cavernous nerve crushing injury. MATERIALS AND METHODS Animals White male Sprague-Dawley rats aged 8 weeks with weight distribution of 300-350 gm were purchased from Saemataco Inc. (Osan, Korea). Then, the rats were divided into 5 groups: the control group (n = 5), the bilateral cavernous nerve crushing group (BCNC group, n = 10), the administration of mesenchymal stem cells following the bilateral cavernous nerve crushing (BCNC with MSCs group, n = 10), the administration of Matrixen following the bilateral cavernous nerve crushing (BCNC with Matrixen group, n = 10), and the administration with MSCs mixed with Matrixen following the bilateral cavernous nerve crushing (BCNC with MSCs/Matrixen group, n = 10). The experimental protocol was approved by the Catholic University Animal Ethics Committee (CUMC-2009-0045-01). Preparation of MSCs For preparation of rat bone marrow-derived MSCs (rBM-MSCs), bone marrow cells were collected from the femurs and tibias of 3-4 week-old Sprague-Dawley rats by fl ushing the respective tissues with Hank’s balanced salt solution (HBSS, WelGENE, Korea) containing 2% fetal bovine serum (FBS; Hyclone, USA). After red blood cells were removed, bone marrow cells were fi ltered through a 40 μm cell strainer (BD Bioscience, San Jose, CA) and separated using Ficoll density gradient centrifugation. Isolated bone marrow cells were re-suspended and cultured in Dulbecco’s Modifi ed Eagle Medium (DMEM, 1000 mg/L glucose; WelGENE) with 20% FBS, 100 U/mL penicillin and 100 g/mL of streptomycin (Invitrogen, Carlsbad, CA) for about 10 days until colonies formed. Colonies were harvested and used for subsequent experiments as MSCs. For animal experiments, ex-vivo expanded MSCs (less than passage 5) were seeded into a 70 mm fl ask at an initial density of 1.4x106 cells and incubated overnight at 37 °C. Cells were then trypsinized, washed with PBS, and injected into the rats (1x106 cells/rat). Bilateral cavernous nerve crushing and administration of MSCs or MSCs mixed with Matrixen Tiletamine (Zoletil) 0.2 mL was injected intraperitoneally to anesthetize the animals. A lower midline incision was made and the prostate gland was exposed. After identifying the major pelvis ganglion (MPG) on the lateral side to biIBJU | MESENCHYMAL STEM CELLS ASSOCIATED TO MATRIXEN ON THE ERECTILE FUNCTION AFTER CAVERNOUS NERVE CRUSHING INJURY 835 lateral prostates, the cavernous nerves, tracking posterolaterally, were identifi ed and isolated. In control group (sham surgery), there was no further surgical manipulation. In the remaining groups the cavernous nerves were isolated and a crush injury was induced using a hemostat clamp for 2 min. In the BCNC group, the abdomen was closed after the bilateral cavernous nerve crushing. In the BCNC with MSCs group, MSCs (1x106 in 20 μL) were administered to the MPG, Matrixen (20 μL) was administered to the MPG, and MSC (1x106 in 20 μL) mixed with Matrixen (Bioland, Cheongwon, Chunbuk, KOREA) administered to the MPG in BCNC with MSCs/Matrixen group after bilateral cavernous nerve crushing (Figure-1). Then a bipolar electrical stimulator was placed on the ganglion to stimulate the cavernous nerve for 50 seconds at 1.5 mA, 20 Hz, pulse width 0.2 ms. The cavernous nerve stimulation was conducted at least 3 times and the interval between stimulations was maintained for over 10 minutes. At the completion of functional analysis, the MPG and penis were excised for histopathology. Immunofl uoescent staining of MSCs in MPG Immediately following ICP measurement, the ganglion was removed. The tissue was then snap frozen using 2-methylbutane pre-cooled in liquid nitrogen. Cryostat sections of the ganglion embedded in tissue-Tek OCT were obtained. From each ganglion, consecutive sections (5 μm) were collected on 4-5 slides, and thus each contained a similar collection of 10-15 serial sections from the same animal. Ganglion sections were washed three times for 5 min with PBS and to avoid nonspecific antibody binding; they were then incubated for 60 min with 2% normal goat serum (Chemicon International, Temecula, CA) containing 0.1% Triton X-100. To evaluate neuronal differentiation of MSCs, the samples were incubated with anti-beta-tublin III (Tuj1) (diluted to 1:200; Abcam, Cambridge, UK) overnight at 4 °C in a humidified chamber. Sections were incubated with the secondary antibody (Alexa Fluor 488 goat anti-rabbit IgG; Invitrogen) for 2 hours in the dark in a humidified chamber at room temperature. After a washing (3 times, 10 min. each) with PBS, the nuclei were counterstained with 4,6-diamino-2-phenylindole dihydrochloride (DAPI;vector Labs, Burlingame, CA). Immunofl uorescence was visualized using an Olympus BX51 fl uorescence microscope. eNOS and nNOS protein expression tests: Western blot The corpus cavernosum was obtained from all rats and homogenized individually in a buffer solution of 0.32M sucrose, 0.2M Hepes, (pH 7.4), 1mM ethylenediaminetetraacetic acid (EDTA), 1mM dithiothreitol (DTT), 10 μg/mL leupeptin, 2 μg/mL aprotinin, 1 μg/mL pepstatin, 10 μg/mL trypsin inhibitor and 1mM phenylmethylsulfonyl Figure 1 The gross fi nding of MSCs plus collagen based cell carrier after immediate administration into MPG. A: MPG of normal rats, B: Gel formation of collagen based cell carrier contacting of MSCs after implantation, MPG: major pelvic ganglion, MSCs: mesenchymal stem cells. Erectile functional assessment The rats were anaesthetized with an intraperitoneal injection of 0.2 mL Tiletamine (Zoletil®). With the rat in the supine position, the penis was dissected and the corpus cavernosum and crus of the penis were exposed. A low, midline abdominal incision was made to access the pelvis, and the MPG lateral to the right prostate was exposed. For the measurement of the intracavernosal pressure (ICP), a heparinized 23G butterfl y needle was inserted in the corpus cavernosum of penile proximal portion after penile skin was degloved and the corpus cavernosum identifi ed. For the measurement of mean arterial pressure (MAP), a PE-50 tube was inserted into the carotid artery. IBJU | MESENCHYMAL STEM CELLS ASSOCIATED TO MATRIXEN ON THE ERECTILE FUNCTION AFTER CAVERNOUS NERVE CRUSHING INJURY 836 fl uoride (PMSF). The homogenized buffer solution was placed on ice for 15 min and centrifuged at 4 oC for 13,000 rpm for 15 minutes. The supernatant solution was separated. The separated solution was utilized in the bovine serum albumin. 30 μg of the quantitative protein was denatured at 95 oC for 5 min. and electrophoresis was performed on a 12% discontinuous sodium dodecylsulfate (SDSPAGE)-polyacrylamide gel. The proteins were then electroblotted onto a 0.2 μm polyvinylidenedifl uoride (PVDF, Amershambioscience, USA) membrane for 150 minutes at 25V. The membranes were reacted with blocking buffer (5% skim milk in TBS-T buffer) for 30 minutes at the ambient temperature. The eNOS and nNOS (BD Biosciences, USA) antibodies were added for 2 hours, and the membrane was washed 3 times using TTBS at intervals of 10 min. The secondary antibodies, anti-mouse IgG-HRP and anti-goat IgG-HRP (1:2000 dilution) (Zymed Laboratories Laboratories, USA) were added at the ambient temperature for 1 hours and the membrane was washed again with TTBS for 6 times with an interval of 5 minutes between each washing. Chemiluminescence was detected using ECL Western blotting detection reagents. Densitometric assessment of the bands on the autoradiogram was performed using Bio1D software (version 97; Vilber Lourmat, France). Statistical analysis All measurements were expressed as mean ± standard deviation (SD). Statistical analysis was obtained via Sigma stat for Windows. An inter-group comparison was made with the use of Neuman-Keuls multiple co


INTRODUCTION
Diagnosis of prostate cancer has been elevating due to the increase in prostate-specifi c antigen (PSA) screening.In addition, this earlier diagnosis increases the number of patients pre-senting with clinically organ-confi ned disease and therefore, it has led to an increase of the number of candidates for radical prostatectomy (1,2).Radical prostatectomy has been associated with complications such as postoperative urinary incontinence and erectile dysfunction.Erectile dysfunction is a bothersome complaint among pa-tients submitted to radical prostatectomy and it is an important reason for the decrease of the quality of life in these patients.Therefore, nerve-sparing procedures have been proposed to reduce short--term and long-term functional complications such as erectile dysfunction (3)(4)(5).However, some patients submitted to radical prostatectomy with nerve-sparing technique have been experiencing erectile dysfunction and need other treatments to improve their symptoms (6).
Mesenchymal derived stem cells (MSCs) from bone marrow seems to be one of the attractive treatments for tissue regeneration and engineering due to their differentiation potentials into various adult tissues, including endothelial cell, smooth muscle and nerve (7).Therefore, there have been several studies using MSCs and the treatment effect of MSCs has been studied in the animal model of erectile dysfunction caused by cavernous nerve injury.As a result, stem cell therapy may be one of the treatment options for the patients that lost their potency after radical prostatectomy.However, some diffi culties appeared in stem cell therapy in spite of their therapeutic effect.For example, stem cells were easily spread-out to the adjacent tissue after stem cell injection into the target tissue according to the report by Lee et al. (8).This may cause unexpected, unfavorable events and moreover, we are not able to get anticipating results from the stem cell therapy, neither.To overcome this weakness, some investigators used polymers to promote the retention of stem cells in the targeted tissue (9)(10)(11).
Among various biomaterials, Matrixen is a collagen based biocompatible polymer and it has been used widely as scaffolds in medical fi eld.In addition, Matrixen is easy to handle depending on the investigator's purpose due to its characteristics of thermo-dependant sol-to-gel transition.Therefore, we used Matrixen to enhance the implantation ability of MSCs and compared the effect of MSCs and MSCs mixed with Matrixen in rats with cavernous nerve crushing injury.

Animals
White male Sprague-Dawley rats aged 8 weeks with weight distribution of 300-350 gm were purchased from Saemataco Inc. (Osan, Korea).Then, the rats were divided into 5 groups: the control group (n = 5), the bilateral cavernous nerve crushing group (BCNC group, n = 10), the administration of mesenchymal stem cells following the bilateral cavernous nerve crushing (BCNC with MSCs group, n = 10), the administration of Matrixen following the bilateral cavernous nerve crushing (BCNC with Matrixen group, n = 10), and the administration with MSCs mixed with Matrixen following the bilateral cavernous nerve crushing (BCNC with MSCs/Matrixen group, n = 10).The experimental protocol was approved by the Catholic University Animal Ethics Committee (CUMC-2009-0045-01).

Preparation of MSCs
For preparation of rat bone marrow--derived MSCs (rBM-MSCs), bone marrow cells were collected from the femurs and tibias of 3-4 week-old Sprague-Dawley rats by fl ushing the respective tissues with Hank's balanced salt solution (HBSS, WelGENE, Korea) containing 2% fetal bovine serum (FBS; Hyclone, USA).After red blood cells were removed, bone marrow cells were fi ltered through a 40 µm cell strainer (BD Bioscience, San Jose, CA) and separated using Ficoll density gradient centrifugation.Isolated bone marrow cells were re-suspended and cultured in Dulbecco's Modifi ed Eagle Medium (DMEM, 1000 mg/L glucose; WelGENE) with 20% FBS, 100 U/mL penicillin and 100 g/mL of streptomycin (Invitrogen, Carlsbad, CA) for about 10 days until colonies formed.Colonies were harvested and used for subsequent experiments as MSCs.For animal experiments, ex-vivo expanded MSCs (less than passage 5) were seeded into a 70 mm fl ask at an initial density of 1.4x106 cells and incubated overnight at 37 °C.Cells were then trypsinized, washed with PBS, and injected into the rats (1x106 cells/rat).

Bilateral cavernous nerve crushing and administration of MSCs or MSCs mixed with Matrixen
Tiletamine (Zoletil) 0.2 mL was injected intraperitoneally to anesthetize the animals.A lower midline incision was made and the prostate gland was exposed.After identifying the major pelvis ganglion (MPG) on the lateral side to bi-lateral prostates, the cavernous nerves, tracking posterolaterally, were identifi ed and isolated.In control group (sham surgery), there was no further surgical manipulation.In the remaining groups the cavernous nerves were isolated and a crush injury was induced using a hemostat clamp for 2 min.In the BCNC group, the abdomen was closed after the bilateral cavernous nerve crushing.In the BCNC with MSCs group, MSCs (1x106 in 20 µL) were administered to the MPG, Matrixen (20 µL) was administered to the MPG, and MSC (1x106 in 20 µL) mixed with Matrixen (Bioland, Cheongwon, Chunbuk, KOREA) administered to the MPG in BCNC with MSCs/Matrixen group after bilateral cavernous nerve crushing (Figure -1).
Then a bipolar electrical stimulator was placed on the ganglion to stimulate the cavernous nerve for 50 seconds at 1.5 mA, 20 Hz, pulse width 0.2 ms.The cavernous nerve stimulation was conducted at least 3 times and the interval between stimulations was maintained for over 10 minutes.At the completion of functional analysis, the MPG and penis were excised for histopathology.

Immunofl uoescent staining of MSCs in MPG
Immediately following ICP measurement, the ganglion was removed.The tissue was then snap frozen using 2-methylbutane pre-cooled in liquid nitrogen.Cryostat sections of the ganglion embedded in tissue-Tek OCT were obtained.From each ganglion, consecutive sections (5 µm) were collected on 4-5 slides, and thus each contained a similar collection of 10-15 serial sections from the same animal.
Ganglion sections were washed three times for 5 min with PBS and to avoid nonspecific antibody binding; they were then incubated for 60 min with 2% normal goat serum (Chemicon International, Temecula, CA) containing 0.1% Triton X-100.To evaluate neuronal differentiation of MSCs, the samples were incubated with anti--beta-tublin III (Tuj1) (diluted to 1:200; Abcam, Cambridge, UK) overnight at 4 °C in a humidified chamber.Sections were incubated with the secondary antibody (Alexa Fluor 488 goat anti-rabbit IgG; Invitrogen) for 2 hours in the dark in a humidified chamber at room temperature.After a washing (3 times, 10 min.each) with PBS, the nuclei were counterstained with 4,6-diamino-2--phenylindole dihydrochloride (DAPI;vector Labs, Burlingame, CA).Immunofl uorescence was visualized using an Olympus BX51 fl uorescence microscope.

Erectile functional assessment
The rats were anaesthetized with an intraperitoneal injection of 0.2 mL Tiletamine (Zole-til®).With the rat in the supine position, the penis was dissected and the corpus cavernosum and crus of the penis were exposed.A low, midline abdominal incision was made to access the pelvis, and the MPG lateral to the right prostate was exposed.For the measurement of the intracavernosal pressure (ICP), a heparinized 23G butterfl y needle was inserted in the corpus cavernosum of penile proximal portion after penile skin was degloved and the corpus cavernosum identifi ed.For the measurement of mean arterial pressure (MAP), a PE-50 tube was inserted into the carotid artery.fl uoride (PMSF).The homogenized buffer solution was placed on ice for 15 min and centrifuged at 4 ºC for 13,000 rpm for 15 minutes.The supernatant solution was separated.The separated solution was utilized in the bovine serum albumin.30 µg of the quantitative protein was denatured at 95 ºC for 5 min.and electrophoresis was performed on a 12% discontinuous sodium dodecylsulfate (SDSPAGE)--polyacrylamide gel.The proteins were then electroblotted onto a 0.2 µm polyvinylidenedifl uoride (PVDF, Amershambioscience, USA) membrane for 150 minutes at 25V.The membranes were reacted with blocking buffer (5% skim milk in TBS-T buffer) for 30 minutes at the ambient temperature.The eNOS and nNOS (BD Biosciences, USA) antibodies were added for 2 hours, and the membrane was washed 3 times using TTBS at intervals of 10 min.The secondary antibodies, anti-mouse IgG-HRP and anti-goat IgG-HRP (1:2000 dilution) (Zymed Laboratories Laboratories, USA) were added at the ambient temperature for 1 hours and the membrane was washed again with TTBS for 6 times with an interval of 5 minutes between each washing.Chemiluminescence was detected using ECL Western blotting detection reagents.Densitometric assessment of the bands on the autoradiogram was performed using Bio1D software (version 97; Vilber Lourmat, France).

Statistical analysis
All measurements were expressed as mean ± standard deviation (SD).Statistical analysis was obtained via Sigma stat for Windows.An inter--group comparison was made with the use of Neuman-Keuls multiple comparison test.The cut-off value of statistical signifi cance was P < 0.05.

Expression of MSCs in MPG using immunofl uoescent staining
MPG in BCNC group showed decreased expression of neuronal cells compared with that of control group.The expression of neuronal cells was increased in BCNC with MSCs and BCNC with MSC/Matrixen groups compared with BCNC group.In the MCSs/Matrixen group, increased implantation of MSCs was observed in MPGs compared with BCNC with MSCs group (Figure -3).

Quantifi cation of eNOS and nNOS proteins
Decreased expressions of eNOS and nNOS were observed in the BCNC and BCNC with Matrixen groups than the control group (P < 0.05).The increase expressions of the eNOS and nNOS was observed in the BCNC with MSC and BCNC with MSCs/Matrixen groups compared with BCNC group (P < 0.05).The signifi cant increase expression of the eNOS and nNOS was observed in BCNC with MSC/Matrixen group compared with BCNC with MSCs group (P < 0.05) (Figure -4).

DISCUSSION
We observed that the administration of MSCs into major pelvic ganglion (MPG) showed the preservation of erectile function after bilateral cavernous nerve crushing injury.Moreover, the implantation of MSCs was enhanced in the MPG with the help of collagen based cell carrier, Matrixen, and the improvements of functional and histological results were noted in this study.
Animal model induced by bilateral cavernous nerve crushing injury has been widely used because this type of injury was designed to mimic the partial nerve damage that occurs during nerve-sparing radical prostatectomy through mechanical nerve stretch (11).And several studies were performed about the periodic changes of MPG in response to the cavernous nerve injury in the animals with erectile dysfunction induced by cavernous nerve injury (12,13).For example, Palma et al. (12) observed the sprouting of injured postganglionic axons in MPG of adult male rats at the fi rst week after unilateral cavernous nerve transaction or crushing.And the recovery of cavernous nerve probably partly depends on sprouting of the remaining neural tissue after adverse manipulation.However, clinically, the recovery of erectile function cannot be observed in all patients who are supposed to experience the partial nerve damage that occurs during nerve-sparing radical prostatectomy (6).As a result, stem cell therapy has been introduced as one of therapeutic options to help the preservation and restoration of erectile function in these patients (4).Therefore, we administered MSCs to MPG to evaluate the infl uence on the recovery of neurogenic erectile dysfunction by bilateral cavernous crushing injury.Moreover, we evaluated the role of Matrixen as a stem cell carrier to promote the implantation ability of MSCs in MPG by administration of MSCs mixed with Matrixen.At 4 weeks after injury, ICP/MAP ratios in BCNC with MSCs and BCNC with MSCs mixed with Matrixen were signifi cantly elevated compared with BCNC group.Even more elevated ICP/ MAP ratio was observed in the BCNC with MSCs/ Matrixen group than in the BCNC with MSCs group.This result supposed that more implantation of MSCs was possible in MPG, since Matrixen prevented the spread-out of MSCs to the adjacent, unexpected area form the MPG.And this result was identifi ed with increased expression of stem cell in MPG in the BCNC with MSCs/Matrixen group compared with the BCNC with MSCs group from the immunofl uorescent staining results.
Currently, MSCs suspended in cell culture medium are administered and therefore, there may be a limitation in the cell retention and transplant survival (15,16).There have been several studies to promote cell survival and retention, for example, the use of biomaterial scaffolds, which provide a microporous framework to improve cell survival (16,17).Xu et al. (9) reported treatment effect of the muscle derived stem cell (MDSC) mixed with fi brin glue on the restoration of urethral sphincter function resulted from the pudendal nerve transaction rat model.They observed an obvious increase of the thickness of muscle mass and of the muscle/collagen ratio, as well as a higher neovasculature density after MDSC mixed with fi brin glue injection.There is another study about the effect of MDSC mixed with polymer such as alginate (Alg)/polycaprolactone (PCL) in the same urethral sphincter dysfunction animal model (10).It also observed signifi cant functional improvement compared with injection with MDSCs, alone and suggested that the polymer may promote the stem cell viability and bulking effect.To be clinically useful cell transplant carriers, there are several required conditions.They need to be biocompatible without toxic side effects and biodegradable.And the ideal preparation must be liquid because liquid would be shaped and administered more easily.
We used Matrixen as stem cell carrier because it is collagen based biocompatible polymer and also shows thermosensitive character.It has easily sol-to-gel transition character that depends on the temperature.Matrixen remains as a sol state at the low temperature; therefore, it can be easily mixed with MSCs.After implantation into MPG with MSCs mixed with Matrixen, we could observe the immediate sol-to-gel transition and the gel formed three-dimensional shape at the body temperature.This means that the gel formation rate is fast.If the process of gel formation is slow Matrixen spreads to form a sheet like structure (19,20) and it may disturb the retention and localization of MSCs in MPG.Therefore, the better preservation of eNOS and nNOS levels in BCNC with MSCs/Matrixen group may be due to the stable immobilization of MSCs by Matrixen in MPG compared with BCNC with MSCs group.In addition, there was a study that suggested the necessity of a cell transplant carrier in other aspect.They observed that relatively large amount of MDSCs was needed for the functional improvement in the rats of intrinsic sphincter defi ciency due to the spread-out of MDSCs (21).Practically, it is impossible to use a large number of MSCs for the regeneration of damaged tissue because the acceptable capacity may be limited according to the size of damaged tissue.However, the administration with Matrixen after BCNC did not show functional and molecular improvement compared with BCNC with MSC/Matrixen group.From this fi nding, we consider that Matrixen does not have a role in the restoration of damaged nerve tissue and its ability seems to be a simple cell carrier to enhance cell implantation.
The safety of MSCs has been well demonstrated (22,23), however, there is a probable chance to occur unexpected adverse events after MSCs treatment.Thus it is important to make MSCs act on the targeted damage tissue as possible and we expect the better treatment outcome of MSCs with the help of transplant cell carrier such as Matrixen.As a result, Matrixen is supposed to enhance the implantation of MSCs and differentiate to neural cells in MPG.

CONCLUSIONS
After administration with MSCs, alone, functional and histological restoration was observed in the rats with bilateral cavernous nerve crushing injury.In addition, the effect of MSCs on recovery of erectile function might be improved by using the cell carrier such as Matrixen.The reason of this result seemed that Matrixen might prevent spread-out of MSCs after administration.Therefore, we considered that the use of transplant cell carrier such as Matrixen may help the implantation of MSCs and improve the therapeutic effect of MSCs.

Figure 1 -
Figure 1 -The gross fi nding of MSCs plus collagen based cell carrier after immediate administration into MPG.A: MPG of normal rats, B: Gel formation of collagen based cell carrier contacting of MSCs after implantation, MPG: major pelvic ganglion, MSCs: mesenchymal stem cells.