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Open AccessJournal ArticleDOI

Transplantation of testis germinal cells into mouse seminiferous tubules.

TLDR
Results indicate that microinjection of cell suspensions into the seminiferous tubules, efferent ducts or rete testis are equally effective in generating donor cell-derived spermatogenesis in recipients.
Abstract
In the adult male, germ cell differentiation takes place in the seminiferous tubules of the testis by a complex, highly organized and very efficient process. A population of diploid stem-cell spermatogonia that lie on the basement membrane of the tubule continuously undergoes self-renewal and produces progeny cells, which initiate the process of cellular differentiation to generate mature spermatozoa. Each testis contains many seminiferous tubules, which are connected at both ends to a collecting system called the rete testis. The mature spermatozoa pass from the tubules into the rete and are then carried through efferent ducts to the epididymis for final maturation before they are ready to fertilize an egg. In previous studies, we have demonstrated that donor testis cells collected from a fertile mouse are able to generate spermatogenesis when transplanted to the seminiferous tubules of an infertile male. The spermatozoa produced by the recipient from the donor-derived spermatogonial stem cells are able to fertilize eggs and produce progeny carrying the donor male haplotype. Furthermore, donor testis stem cells from a rat will generate normal rat spermatozoa following transplantation to a mouse testis. The spermatogonial transplantation technique is clearly valuable and applicable to many species, but it is difficult. Therefore, several procedures to introduce donor cells into the seminiferous tubules of a recipient have been developed using the mouse as a model, and they are described here in detail. The results indicate that microinjection of cell suspensions into the seminiferous tubules, efferent ducts or rete testis are equally effective in generating donor cell-derived spermatogenesis in recipients. Each approach is likely to be useful for different experimental purposes in a variety of species.

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Journal ArticleDOI

Reconstitution of the Mouse Germ Cell Specification Pathway in Culture by Pluripotent Stem Cells

TL;DR: The generation of primordial germ cell-like cells (PGCLCs) in mice with robust capacity for spermatogenesis is demonstrated and provided a paradigm for the first step of in vitro gametogenesis.
Journal ArticleDOI

Long-Term Proliferation in Culture and Germline Transmission of Mouse Male Germline Stem Cells

TL;DR: In vitro culture of spermatogonial stem cells that proliferate for long periods of time are reported, and gonocytes isolated from neonatal mouse testis proliferated over a 5-month period and restored fertility to congenitally infertile recipient mice following transplantation into seminiferous tubules.
Journal ArticleDOI

β1- and α6-integrin are surface markers on mouse spermatogonial stem cells

TL;DR: Spermatogonial stem cell-associated antigens are demonstrated by using an assay system based on biological function and suggest that these cells share elements of a common molecular machinery with stem cells in other tissues.
Journal ArticleDOI

Spermatogonial Stem Cells

TL;DR: It has become abundantly clear that at least mouse SSCs can become multipotent embryonic stem–like cells again, capable of differentiation into many other cell lineages and whether the latter is also possible for human SSC.
Journal ArticleDOI

Spermatogonial stem cells share some, but not all, phenotypic and functional characteristics with other stem cells.

TL;DR: The identification of a surface phenotype that allows production of a highly enriched SSC population will facilitate functional and genomic studies and enable further comparison with other stem cells.
References
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Journal ArticleDOI

Spermatogenesis following male germ-cell transplantation

TL;DR: It is reported here that stem cells isolated from testes of donor male mice will repopulate sterile testes when injected into seminiferous tubules and may prove useful as a tool for biomedical science and biotechnology.
Journal ArticleDOI

Spermatogenic cells of the prepuberal mouse. Isolation and morphological characterization.

TL;DR: The successful isolation of these prepuberal cell types was accomplished by defining distinctive morphological characteristics of the cells and assessing the identity and purity of the isolated cell types by microscopy.
Journal ArticleDOI

Kinetics of spermatogenesis in mammals: seminiferous epithelium cycle and spermatogonial renewal.

Y Clermont
TL;DR: The kinetics of sperMatogenesis in mammals are reviewed with special emphasis on the seminiferous epithelium cycle and spermatogonial renewal .
Journal ArticleDOI

A role for CD95 ligand in preventing graft rejection.

TL;DR: CD95 ligand expression in the testis probably acts by inducing apoptotic cell death of CD95-expressing, recipient T cells activated in response to graft antigens, and indicates that CD 95 ligand could be used to create immune-privileged tissue for a variety of transplant uses.
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