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Meiotic Arrest and Germ Cell Apoptosis in Androgen-Binding Protein Transgenic Mice¹

Unitat de Recerca Biomèdica (D.M.S., O.M.T., J.R., F.M.) and the Departament d’Anatomia Patològica (N.T.), Hospital Materno-Infantil Vall d’Hebron, 08035 Barcelona, Spain; and the Department of Cell Biology, Georgetown University Medical Center (C.A.S.-Q.), Washington, D.C. 20007

Address all correspondence and requests for reprints to: Dr. Jaume Reventós, Unitat de Recerca Biomèdica, Hospital Materno-Infantil Vall d’Hebrón, Ps. Vall d’Hebrón, 119–129, 08035 Barcelona, Spain. E-mail: reventos{at}hg.vhebron.es

The fundamental role of androgen-binding protein (ABP) in spermatogenesis remains obscure after nearly 25 yr since its first characterization. In the present investigation, we used a transgenic mouse model that overexpresses rat ABP to examine the potential involvement of this protein in the regulation of processes occurring during spermatogenesis. Specifically, homozygous or heterozygous transgenic mice were analyzed in terms of spermatogenic progression, DNA fragmentation pattern, and germinal cell ploidy status.

All animals homozygous for transgenic ABP exhibited an increased accumulation of primary spermatocytes and cells at metaphase with abnormal morphology and localization within the seminiferous epithelium. Analysis of DNA fragmentation by in situ techniques and agarose gel electrophoresis provided evidence for an increased occurrence of apoptosis in the transgenic animals, principally involving pachytene spermatocytes and cells at metaphase. Flow cytometric analysis of the DNA content of isolated germ cells revealed a reduction in the number of haploid cells, an increase in the number of tetraploid cells, and the appearance of a hypotetraploid cell population, consistent with degenerating primary spermatocytes. In mice heterozygous for the transgene, the effects were less prominent, and the degree to which spermatogenesis was compromised correlated with the levels of ABP messenger RNA in individual animals. The present results are interpreted to suggest that ABP can act as a modulator of spermatogenesis by regulating completion of the first meiotic division of primary spermatocytes.

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