Benzo[a]pyrene‐decreased gap junctional intercellular communication via calcium/calmodulin signaling increases apoptosis in TM4 cells |
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| Authors: | Xiaoli Ji Xin Chou Zehe Ge Fan Ding Hui Gao Qing Wu |
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| Affiliation: | School of Public Health, Fudan University and Key Laboratory of Public Health Safety, Ministry of Education, Shanghai, China |
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| Abstract: | The mechanism of male reproductive toxicity induced by benzo[a]pyrene (BaP) is poorly understood. Gap junctional intercellular communication (GJIC) is known to play a critical role in maintaining spermatogenesis. The aim of the present study was to determine the toxic effects of BaP in Sertoli cells, and to explore the possibility and potential mechanisms of BaP‐induced changes in the level of GJIC, and the relationship between GJIC and BaP‐induced apoptosis. We treated mouse Sertoli cell lines (TM4) with different concentrations (0.1–100 μm ) of BaP for 1–48 hours, and found that GJIC exhibited a dose‐ and time‐dependent downregulation. Treatment with 10 μm BaP increased apoptosis, intracellular Ca2+ level ([Ca2+]i) and calmodulin (CaM) protein expression, and decreased the protein level of connexin 43 (Cx43) (also known as gap junction α‐1 protein [GJA1]) in TM4 cells. However, BaP had no effect on the phosphorylation of Cx43 at Ser279/282, Ser255, Ser368 or Ser262. Downregulation of [Ca2+]i by BAPTA‐AM significantly attenuated the BaP‐induced GJIC suppression, Cx43 protein decrease and CaM protein increase. Interestingly, inhibition of CaM expression by W7 partially recovered BaP‐induced GJIC inhibition, but had no effect on BaP‐induced Cx43 protein decrease. Pretreatment with the GJIC activator retinoic acid significantly mitigated BaP‐induced apoptosis. In conclusion, these results suggest that BaP can decrease GJIC via Ca2+/CaM signaling, and that BaP‐induced GJIC suppression increases apoptosis in TM4 cells. |
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| Keywords: | apoptosis benzo[a]pyrene gap junctional intercellular communication intracellular Ca2+ homeostasis Sertoli cells |
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