Transplantation of Autologous Bone Marrow Mesenchymal Stem Cells into the Testes of Infertile Male Rats and New Germ Cell Formation.
- Author:
Mohammad GHASEMZADEH-HASANKOLAEI
1
;
Roozali BATAVANI
;
Mohamadreza Baghaban ESLAMINEJAD
;
Foroughazam SAYAHPOUR
Author Information
- Publication Type:Original Article
- Keywords: Autologous; Bone marrow mesenchymal stem cells; Infertile male rats; Transplantation; Testis; Germ cells
- MeSH: Anesthesia; Animals; Basement Membrane; Bone Marrow*; Epithelium; Germ Cells*; Humans; Infertility, Male; Male*; Mesenchymal Stromal Cells*; Rats*; Regeneration; Seminiferous Tubules; Sertoli Cells; Spermatogenesis; Spermatogonia; Stem Cells; Testis*; Tibia; Transplantation; Vimentin
- From:International Journal of Stem Cells 2016;9(2):250-263
- CountryRepublic of Korea
- Language:English
- Abstract: BACKGROUND: Mesenchymal stem cells (MSCs), have been suggested as a potential choice for treatment of male infertility. Yet, the effects of MSCs on regeneration of germinal epithelium of seminiferous tubules and recovery of spermatogenesis have remained controversial. In this research, we have evaluated and compared the fate of autologous bone marrow (BM)-MSCs during three different periods of time- 4, 6 and 8 weeks after transplantation into the testes of busulfan-induced infertile male rats. METHODS: Rats BM samples were collected from tibia bone under anesthesia. The samples were directly cultured in culture medium. Isolated, characterized and purified BM-MSCs were labeled with PKH26, and transplanted into the testes of infertile rats. After 4, 6 and 8 weeks, the testes were removed and underwent histological evaluations. RESULTS: Immunohistochemical analysis showed that transplanted BM-MSCs survived in all three groups. Some of the cells homed at the germinal epithelium and expressed spermatogonia markers (Dazl and Stella). The number of homed spermatogonia-like cells in 4-week testes, was more than the 6-week testes. The 8-week testes had the least numbers of homed cells (p<0.05). Immunostaining for vimentin showed that BM-MSCs did not differentiate into the sertoli cells in the testes. CONCLUSIONS: From our results, it could be concluded that, autologous BM-MSCs could survive in the testis, migrate onto the seminiferous tubules basement membrane and differentiate into spermatogonia. Although, no more differentiation was observed in the produced spermatogonia, generation of such endogenous GCs would be a really promising achievement for treatment of male infertility using autologous stem cells.
