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Regular Article |
a Department of Cell and Developmental Biology and The Laboratories for Reproductive Biology, University of North Carolina, Chapel Hill, North Carolina 27599
Transgenic mice carrying rat androgen-binding protein (ABP) genomic DNA express high amounts of testicular ABP and develop a progressive impairment of spermatogenesis. To understand the mechanism of these changes, we have studied the pattern of testicular germ cell proliferation from 7 to 360 days of age in wild-type (WT) control and transgenic homozygous (ABP-TG) mice by flow cytometry after labeling DNA in isolated germ cells with propidium iodide. At all ages studied, the body weight of the ABP-TG mice was lower than that of age-matched WT controls. Significantly reduced testicular weight and total germ cell number in the ABP-TG mice were evident from Day 30 and Day 60, respectively. Flow cytometric analysis of isolated germ cells revealed that the number of germ cells undergoing proliferation (S-phase cells) was identical in WT control and ABP-TG mice up to Day 14. Subsequently, the number of germ cells in S-phase was consistently higher in ABP-TG than in WT mice. The number of primary spermatocytes was significantly increased starting from Day 60, and the numbers of round and elongated spermatids were significantly reduced in the ABP-TG animals from Day 21 and Day 60 onwards, respectively. Immunocytometry for intracellular ABP at 90 days of age revealed that the percentage of ABP-containing germ cells was greater in ABP-TG than in WT mice. The continuous presence of ABP in mouse seminiferous tubules at greater than physiological concentrations facilitates the formation of primary spermatocytes but impairs subsequent transformation to round and elongated spermatids. Based on our observations and the analysis of the available literature, the most likely mechanism for production of these effects is sustained reduction in the bioavailability of androgens.
1 This work was supported in part by grants from The Fogarty International Center (D43 TW/HD00627 to D.A.J.) and NICHD/NIH (HD 35693 to P.P.) and through cooperative agreement U54-HD35041 as part of the Specialized Cooperative Centers Program in Reproduction Research.
2 Correspondence: Peter Petrusz, Department of Cell and Developmental Biology, University of North Carolina, CB 7090, 108 Taylor Hall, Chapel Hill, NC 27599. FAX: 919 966 1856; petrusz{at}med.unc.edu
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