| Literature DB >> 21524277 |
Yue Huang1, Xia Mao, Terry Boyce, Guo-Zhang Zhu.
Abstract
PTEN (phosphatase and tensin homologue deleted on chromosome ten) plays critical roles in multiple cellular processes, including cell proliferation, survival, migration and transformation. A role of PTEN in mammalian spermatogenesis, however, has not been explored. To address this question, we generated a mouse model with PTEN conditional knockout in postnatal male germ cells. We found that spermatogenesis was normal in PTEN-deleted male germ cells. PTEN conditional mutant males produced sperm and sired offspring as competently as wild-type littermates. Moreover, our biochemical analysis also indicated that the Akt (acutely transforming retrovirus AKT8 in rodent T cell lymphoma) signalling pathway was not affected in mutant testis. Taken together, these findings demonstrate that PTEN is dispensable in mouse spermatogenesis.Entities:
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Year: 2011 PMID: 21524277 PMCID: PMC4526189 DOI: 10.1042/CBI20110161
Source DB: PubMed Journal: Cell Biol Int ISSN: 1065-6995 Impact factor: 3.612