Spermatogenesis following male germ-cell transplantation (spermatogonia/stem cells/testes/transgenic mice)

Spermatogenesis following male germ-cell transplantation (spermatogonia/stem cells/testes/transgenic mice)

Vol. 91, pp. 11298–11302, November 1994 | RALPH L. BRINSTER* AND JAMES W. ZIMMERMANN†
The study by Ralph L. Brinster and James W. Zimmermann reports the successful transplantation of stem cells from donor male mice into the seminiferous tubules of recipient testes, leading to the establishment of normal spermatogenesis and the production of mature spermatozoa. The researchers isolated stem cells from the testes of donor mice and injected them into the seminiferous tubules of recipient testes. The transplanted donor cells demonstrated normal morphological characteristics and produced mature spermatozoa, indicating that the stem cell population can self-renew and differentiate into sperm cells in a new environment. This technique not only opens new avenues for basic research on spermatogenesis and stem-cell self-renewal but also has potential applications in biomedical science and biotechnology. The study used two protocols: one involving C57BL/6 donor mice and W/W recipient mice, and another using busulfan-treated C57BL/6 × SJL mice as recipients. Both protocols showed successful colonization of recipient testes by donor cells, with up to 10% of the tubules demonstrating some degree of spermatogenesis. The findings suggest that stem cell spermatogonia can be harvested, maintained, and transferred to create new sources of genetic material for further research and applications.The study by Ralph L. Brinster and James W. Zimmermann reports the successful transplantation of stem cells from donor male mice into the seminiferous tubules of recipient testes, leading to the establishment of normal spermatogenesis and the production of mature spermatozoa. The researchers isolated stem cells from the testes of donor mice and injected them into the seminiferous tubules of recipient testes. The transplanted donor cells demonstrated normal morphological characteristics and produced mature spermatozoa, indicating that the stem cell population can self-renew and differentiate into sperm cells in a new environment. This technique not only opens new avenues for basic research on spermatogenesis and stem-cell self-renewal but also has potential applications in biomedical science and biotechnology. The study used two protocols: one involving C57BL/6 donor mice and W/W recipient mice, and another using busulfan-treated C57BL/6 × SJL mice as recipients. Both protocols showed successful colonization of recipient testes by donor cells, with up to 10% of the tubules demonstrating some degree of spermatogenesis. The findings suggest that stem cell spermatogonia can be harvested, maintained, and transferred to create new sources of genetic material for further research and applications.
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