PMID:16270031

Citation	Coultas, L, Bouillet, P, Loveland, KL, Meachem, S, Perlman, H, Adams, JM and Strasser, A (2005) Concomitant loss of proapoptotic BH3-only Bcl-2 antagonists Bik and Bim arrests spermatogenesis. EMBO J. 24:3963-73
Abstract	The BH3-only proteins of the Bcl-2 family initiate apoptosis through the activation of Bax-like relatives. Loss of individual BH3-only proteins can lead either to no phenotype, as in mice lacking Bik, or to marked cell excess, as in the hematopoietic compartment of animals lacking Bim. To investigate whether functional redundancy with Bim might obscure a significant role for Bik, we generated mice lacking both genes. The hematopoietic compartments of bik-/-bim-/- and bim-/- mice were indistinguishable. However, although testes develop normally in mice lacking either Bik or Bim, adult bik-/-bim-/- males were infertile, with reduced testicular cellularity and no spermatozoa. The testis of young bik-/-bim-/- males, like those lacking Bax, exhibited increased numbers of spermatogonia and spermatocytes, although loss of Bik plus Bim blocked spermatogenesis somewhat later than Bax deficiency. The initial excess of early germ cells suggests that spermatogenesis fails because supporting Sertoli cells are overwhelmed. Thus, Bik and Bim share, upstream of Bax, the role of eliminating supernumerary germ cells during the first wave of spermatogenesis, a process vital for normal testicular development.
Links	PubMed PMC1283956 Online version:10.1038/sj.emboj.7600857
Keywords	Adaptor Proteins, Signal Transducing/genetics; Adaptor Proteins, Signal Transducing/metabolism; Animals; Apoptosis/physiology; Apoptosis Regulatory Proteins/genetics; Apoptosis Regulatory Proteins/metabolism; Fertility; Germ Cells/cytology; Germ Cells/metabolism; Hematopoietic Stem Cells/cytology; Hematopoietic Stem Cells/metabolism; Male; Membrane Proteins/genetics; Membrane Proteins/metabolism; Mice; Mice, Inbred C57BL; Mice, Knockout; Mitochondrial Proteins/genetics; Mitochondrial Proteins/metabolism; Organ Size; Phenotype; Proto-Oncogene Proteins/genetics; Proto-Oncogene Proteins/metabolism; Proto-Oncogene Proteins c-bcl-2/genetics; Proto-Oncogene Proteins c-bcl-2/metabolism; Proto-Oncogene Proteins c-kit/metabolism; Spermatogenesis/physiology; Spermatozoa/cytology; Spermatozoa/metabolism; Testis/cytology; Testis/metabolism
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