Immature rat seminiferous tubules reconstructed in vitro express markers of Sertoli cell maturation after xenografting into nude mouse hosts

• Published in: Molecular human reproduction 2010-02, Vol.16 (2), p.97-110
• Main Authors: Gassei, K., Ehmcke, J., Wood, M.A., Walker, W.H., Schlatt, S.
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; Cell Differentiation - genetics; Cell Differentiation - physiology; Cell Proliferation; Embryology: invertebrates and vertebrates. Teratology; Fundamental and applied biological sciences. Psychology; Male; Mice; Mice, Nude; Microscopy, Confocal; Rats; Reverse Transcriptase Polymerase Chain Reaction; Seminal Vesicles - anatomy & histology; Seminal Vesicles - cytology; Seminiferous Tubules - cytology; Seminiferous Tubules - metabolism; Sertoli cell; Sertoli Cells - cytology; Sertoli Cells - metabolism; testicular development; three-dimensional cell culture; Transplantation, Heterologous - methods; xenografting
• ISSN: 1360-9947; 1460-2407
• DOI: 10.1093/molehr/gap081

Sertoli cells undergo a maturation process during post-natal testicular development that leads to the adult-type Sertoli cell, which is required for spermatogenesis. Understanding Sertoli cell maturation is therefore necessary to gain insight into the underlying causes of impaired spermatogenesis and male infertility. The present study characterized the cellular and molecular differentiation of Sertoli cells in a xenograft model of mammalian testicular development. Immature rat Sertoli cells were cultured in a three-dimensional culture system to allow the formation of cord-like structures. The in vitro Sertoli cell cultures were then grafted into nude mice. Sertoli cell proliferation, morphological differentiation and mRNA expression of Sertoli cell maturation markers were evaluated in xenografts. Sertoli cell proliferation significantly decreased between 1 and 4 weeks (6.7 ± 0.9 versus 1.2± 0.1%, P < 0.001), and was maintained at low levels thereafter. Sertoli cell cord-like structures significantly decreased between 1 and 4 weeks (59.6 versus 21%, P < 0.05), whereas Sertoli cell tubules were more frequently observed after 4 weeks (13.3 versus 73.1%, P < 0.05). Furthermore, expression of androgen binding protein, transferrin and follicle stimulating hormone receptor, markers for mature Sertoli cells, was detected after 1 week of grafting and increased significantly thereafter. We conclude from these results that rat Sertoli cells continue maturation after xenografting to the physiological environment of a host. This model of in vitro tubule formation will be helpful in future investigations addressing testicular maturation in the mammalian testis.