Kim G H, Wright W W
Department of Population Dynamics, School of Hygiene and Public Health, The Johns Hopkins University, Baltimore, Maryland 21205, USA.
Biol Reprod. 1997 Dec;57(6):1467-77. doi: 10.1095/biolreprod57.6.1467.
We have examined the effects of maturation and aging on expression of cyclic protein-2 (CP-2)/cathepsin L mRNA by rat Sertoli cells. During maturation (25-68 days of age) there was a significant, 7.6-fold increase in CP-2/cathepsin L mRNA. There was a significant, 2.9-fold increase in SGP-2 mRNA during the same period. In situ hybridization analysis demonstrated that stage-specific expression of CP-2/cathepsin L mRNA developed between 30 and 35 days. By 64 days of age, this transcript was only detectable in Sertoli cells within stage VI-VII tubules. Northern blot analysis of 23-mo-old testes revealed statistically significant decreases in total testis contents of CP-2/cathepsin L and SGP-2 mRNAs (4- and 3-fold, respectively) in testes that lacked germ cells but not in aged testes with a full complement of germ cells. In situ hybridization analysis revealed high amounts of CP-2/cathepsin L mRNA in all aged tubules that were losing germ cells via apoptosis, regardless of the stage of the cycle. Immunocytochemical analysis demonstrated that in these aged, regressing tubules, CP-2/cathepsin L protein became concentrated in dying or dead germ cells.