Establishment of in vitro spermatogenesis from spermatocytes in the medaka, Oryzias latipes

• Published in: Development, growth & differentiation Vol. 39; no. 3; pp. 337 - 344
• Main Authors: Saiki, Atsusi, Tamura, Masaru, Matsumoto, Masami, Katowgi, Jun, Watanabe, Akihiko, Onitake, Kazuo
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Science Pty 01-06-1997
• Subjects: Animals; cell culture; Cell Differentiation; Cells, Cultured; Female; Fertility; fertilization; Haploidy; In Vitro Techniques; Male; Marine; medaka; Meiosis; Microscopy, Electron, Scanning; Oryzias - genetics; Oryzias - growth & development; Oryzias - metabolism; Oryzias latipes; protamine; Protamines - genetics; RNA, Messenger - genetics; RNA, Messenger - metabolism; Spermatocytes - cytology; Spermatocytes - metabolism; spermatogenesis; Spermatogenesis - genetics
• ISSN: 0012-1592; 1440-169X
• DOI: 10.1046/j.1440-169X.1997.t01-2-00009.x

Spermatocytes of the teleost, Oryzias latipes, at meiotic prophase were cultured without contact with somatic cells. They began to divide, progressing through the meiotic divisions and differentiating into round spermatids within 48 h. The chromosome number in both the primary and secondary spermatocytes at metaphase was n= 24. In spermatids, a single flagellum was formed and the release of residual bodies was observed in vitro. The size and shape of the flagellum were the same as those seen in vivo. The expression of protamine mRNA was detected in round spermatids. This result suggests that gene expression, as well as morphological change, is regulated by the progression of spermatogenesis in cell culture. Furthermore, when the eggs of O. latipes were inseminated with germ cells cultured for 10 days, normal embryos developed and hatched out. These results suggest that the spermatocytes of O. latipes develop into fertile sperm in cell culture.