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Biology of Reproduction 59, 1371-1377 (1998)
©Copyright 1998 Society for the Study of Reproduction, Inc.

Germ Cell Genotype Controls Cell Cycle during Spermatogenesis in the Rat1

Luiz R. Françaa, Takehiko Ogawab, Mary R. Avarbockb, Ralph L. Brinsterb, and Lonnie D. Russell2,c

a Department of Morphology, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil 31270-901 CP 486 b School of Veterinary Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104 c Department of Physiology, Southern Illinois University School of Medicine, Carbondale, Illinois 62901-6512

Spermatogenesis is one of the most productive self-renewing systems in the body: on the order of 107 spermatozoa are produced daily per gram of testis tissue. In each mammalian species, the time required for completion of the process is unique and unalterable. Because the process is supported by somatic Sertoli cells, it has generally been thought that cell-cell interaction between germ and Sertoli cells controls the duration of cell cycles and cellular organization. We have used the newly developed technique of spermatogonial transplantation to examine which cell type(s) determines the rate at which germ cells proceed through spermatogenesis. Rat germ cells were transplanted into a mouse testis, and the mouse was killed 12.9–13 days after administration of a single dose of [3H]thymidine. The most advanced rat cell type labeled was the pachytene spermatocyte at stages VI–VIII of the spermatogenic cycle. In animals given only rat cells, some endogenous spermatogenesis of the mouse recovered. The most advanced labeled mouse cell types in recipients killed 12.9–13 days after administration of a single dose of [3H]thymidine were meiotic cells or young spermatids, which is consistent with a spermatogenic cycle length comparable to the 8.6 days reported for the mouse. The same results were obtained if a mixture of rat and mouse cells were transplanted. There existed two separate timing regimens for germ cell development in the recipient mouse testis; one of rat and one of mouse duration. Rat germ cells that were supported by mouse Sertoli cells always differentiated with cell cycle timing characteristic of the rat and generated the spermatogenic structural pattern of the rat, demonstrating that the cell differentiation process of spermatogenesis is regulated by germ cells alone.

1 Editor's Note: The research results described in this paper and its companion (Biol Reprod 1998; 59:1360–1370) were presented, in part, as a State-of-the-Art Lecture at the 31st Annual Meeting of the Society for the Study of Reproduction held at Texas A&M University, College Station, Texas, August 8–11, 1998. Both papers represent original research and have undergone stringent peer review.Support of the Brazilian Research Foundation (CNPq) and the State Research Foundation of Minas Gerais (FAPEMIG) are gratefully acknowledged. Financial support was also received from the National Institutes of Health (HD 36504 and HD35494), USDA/NRI Competitive Grants Program, Commonwealth and General Assembly of Pennsylvania, and the Robert J. Kleberg, Jr. and Helen C. Kleberg Foundation.

2 Correspondence. FAX: 618 453 1517; lrussell{at}som.siu.edu




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Copyright © 1998 by the Society for the Study of Reproduction.