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

Mol Endocrinol. 2000 May;14(5):682-99. doi: 10.1210/mend.14.5.0443.

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.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetates / pharmacology
  • Animals
  • Apoptosis Regulatory Proteins
  • Apoptosis* / drug effects
  • Apoptosis* / physiology
  • Follicle Stimulating Hormone / pharmacology
  • Gene Expression Regulation, Developmental / drug effects
  • Leydig Cells / chemistry
  • Macromolecular Substances
  • Male
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Mesylates / pharmacology
  • Mice
  • Mice, Knockout
  • Proteins / genetics
  • Proteins / metabolism*
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / metabolism*
  • Proto-Oncogene Proteins c-bcl-2*
  • RNA, Messenger / analysis
  • Rats
  • Rats, Sprague-Dawley
  • Sertoli Cells / chemistry
  • Spermatocytes / cytology*
  • Spermatocytes / metabolism
  • Spermatogonia / cytology*
  • Spermatogonia / metabolism
  • Subcellular Fractions / metabolism
  • Testis / cytology*
  • Testis / growth & development
  • Testis / metabolism
  • Testosterone / pharmacology
  • bcl-2 Homologous Antagonist-Killer Protein
  • bcl-2-Associated X Protein

Substances

  • Acetates
  • Apoptosis Regulatory Proteins
  • BCL2L2 protein, human
  • Bak1 protein, mouse
  • Bak1 protein, rat
  • Bax protein, mouse
  • Bax protein, rat
  • Bcl2l2 protein, mouse
  • Bcl2l2 protein, rat
  • Macromolecular Substances
  • Membrane Proteins
  • Mesylates
  • Proteins
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • RNA, Messenger
  • bcl-2 Homologous Antagonist-Killer Protein
  • bcl-2-Associated X Protein
  • Testosterone
  • Follicle Stimulating Hormone
  • ethylene dimethanesulfonate
  • methoxyacetic acid