Bcl-w forms complexes with Bax and Bak, and elevated ratios of Bax/Bcl-w and Bak/Bcl-w correspond to spermatogonial and spermatocyte apoptosis in the testis
- PMID: 10809232
- DOI: 10.1210/mend.14.5.0443
Bcl-w forms complexes with Bax and Bak, and elevated ratios of Bax/Bcl-w and Bak/Bcl-w correspond to spermatogonial and spermatocyte apoptosis in the testis
Abstract
Bcl-w, a prosurvival member of the Bcl-2 family, is essential for spermatogenesis. However, the mechanisms by which Bcl-w participates in the regulation of apoptosis in the testis are largely unknown. To explore the potential role of Bcl-w in the regulation of apoptosis in the testis, the expression of Bcl-w mRNA and protein during testicular development and spermatogenesis, the dimerization with the proapoptosis members of the Bcl-2 family, and the responses to hormonal stimulation in vitro and apoptosis-inducing signals in vivo were investigated. Both Bcl-w mRNA and protein were detected in Sertoli cells, spermatogonia, and spermatocytes, as well as in Leydig cells. The steady-state levels of Bcl-w mRNA and protein were much higher in Sertoli cells than in spermatogonia and spermatocytes. In the adult rat testis, both Bcl-w mRNA and protein in Sertoli cells displayed a stage-specific expression pattern. Bcl-w could form complexes with Bax and Bak but not with Bad. Bax and Bak were immunohistochemically localized to the same cell types as Bcl-w, but with higher expression levels in spermatocytes and spermatogonia than in Sertoli cells. FSH could up-regulate Bcl-w mRNA levels in the seminiferous tubules cultured in vitro, whereas no effect was observed when testosterone was applied. Three animal models that display spermatogonial apoptosis induced by blockade of stem cell factor/c-kit interaction by a function-blocking anti-c-kit antibody, spermatocyte apoptosis induced by methoxyacetic acid, and apoptosis of spermatogonia, spermatocytes, and spermatids induced by testosterone withdrawal after ethylene dimethane sulfonate treatment were employed to check the changes of Bcl-w, Bax, and Bak protein levels during apoptosis of specific germ cells. In all three models, the ratios of Bax/Bcl-w and Bak/Bcl-w were significantly elevated. The present study suggests that Bcl-w is an important prosurvival factor of Sertoli cells, spermatogonia, and spermatocytes and participates in the regulation of apoptosis by binding proapoptotic factors Bax and Bak. The ratios of Bax/Bcl-w and Bak/Bcl-w may be decisive for the survival of Sertoli cells, spermatogonia, and spermatocytes.
Similar articles
-
Bax-dependent spermatogonia apoptosis is required for testicular development and spermatogenesis.Biol Reprod. 2002 Apr;66(4):950-8. doi: 10.1095/biolreprod66.4.950. Biol Reprod. 2002. PMID: 11906913
-
Involvement of Bcl-2 family proteins in germ cell apoptosis during testicular development in the rat and pro-survival effect of stem cell factor on germ cells in vitro.Mol Cell Endocrinol. 2000 Jul 25;165(1-2):115-29. doi: 10.1016/s0303-7207(00)00257-4. Mol Cell Endocrinol. 2000. PMID: 10940490
-
Germ cell apoptosis and expression of Bcl-2 and Bax in porcine testis under normal and heat stress conditions.Acta Histochem. 2017 Apr;119(3):198-204. doi: 10.1016/j.acthis.2016.09.003. Epub 2017 Mar 6. Acta Histochem. 2017. PMID: 28279507
-
Cell proliferation in the mammalian testis: biology of the seminiferous growth factor (SGF).Recent Prog Horm Res. 1984;40:531-67. doi: 10.1016/b978-0-12-571140-1.50017-7. Recent Prog Horm Res. 1984. PMID: 6435219 Review. No abstract available.
-
Spermatogenesis by Sisyphus: proliferating stem germ cells fail to repopulate the testis after 'irreversible' injury.Adv Exp Med Biol. 2001;500:421-8. doi: 10.1007/978-1-4615-0667-6_64. Adv Exp Med Biol. 2001. PMID: 11764975 Review.
Cited by
-
Testicular germ cell tumours: predisposition genes and the male germ cell niche.Nat Rev Cancer. 2011 Apr;11(4):278-88. doi: 10.1038/nrc3021. Epub 2011 Mar 17. Nat Rev Cancer. 2011. PMID: 21412254 Review.
-
Spermatogenesis in Bclw-deficient mice.Biol Reprod. 2001 Jul;65(1):318-32. doi: 10.1095/biolreprod65.1.318. Biol Reprod. 2001. PMID: 11420255 Free PMC article.
-
The genomic landscape of testicular germ cell tumours: from susceptibility to treatment.Nat Rev Urol. 2016 Jul;13(7):409-19. doi: 10.1038/nrurol.2016.107. Epub 2016 Jun 14. Nat Rev Urol. 2016. PMID: 27296647 Review.
-
Exploring the molecular aspects associated with testicular germ cell tumors: a review.Oncotarget. 2017 Nov 3;9(1):1365-1379. doi: 10.18632/oncotarget.22373. eCollection 2018 Jan 2. Oncotarget. 2017. PMID: 29416701 Free PMC article. Review.
-
Molecular biology of testicular germ cell tumors.Clin Transl Oncol. 2016 Jun;18(6):550-6. doi: 10.1007/s12094-015-1423-7. Epub 2015 Oct 19. Clin Transl Oncol. 2016. PMID: 26482724 Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials