Involvement of CaM-CaMKII-ERK in bisphenol A-induced Sertoli cell apoptosis

Toxicology. 2014 Oct 3:324:27-34. doi: 10.1016/j.tox.2014.06.001. Epub 2014 Jun 4.

Abstract

Bisphenol A (BPA), one of the most prevalent chemicals for daily use, has been reported as a xenoestrogen to induce reproductive toxicity, but its mechanism is poorly understood. In the present study, we aimed to explore whether CaM-CaMKII-ERK1/2 signaling pathway was involved in BPA-induced Sertoli cells injury via the mitochondrial apoptotic pathway. TM4 cells were cultured with 0, 0.02, 0.2, 2.0, 20μM BPA, and cell viability, mitochondrial function and CaM-CaMKII-ERK1/2 signal pathway were examined. With the MTT assay, BPA was found to suppress cell viability in a dose- and time-dependent manner. Moreover, mitochondrial mass loss, membrane potential decrease, cytochrome c release, Bcl-2 family members down-regulation and caspases-3 up-regulation were obviously observed when the TM4 cells were exposed to BPA. Additionally, the expression of calmodulin (CaM) and phosphorylation of calcium/calmodulin dependent kinase II (CaMKII) significantly increased, and pretreatment with 10μM antagonist of CaM (W-7) or CaMKII (KN62) prevented cell damage through mitochondrial apoptotic pathway. In parallel, ERK1/2 pathway was proved to participate in BPA-induced cell damage, since W-7 and KN62 partially suppressed ERK1/2 activation, and PD98059, the ERK1/2 antagonist, significantly attenuated BPA-induced cell damage. These data, taken together, indicated that CaM-CaMKII-ERK axis might transmit apoptotic signals to the mitochondria during BPA-induced cell apoptosis. By exploring the mechanisms of the Ca(2+) homeostasis and the corresponding proteins, our study provides new insight into BPA-induced reproductive toxicity.

Keywords: Apoptosis; Bisphenol A; Calcium/calmodulin dependent protein kinase II; Calmodulin; ERK1/2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects*
  • Benzhydryl Compounds / toxicity*
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2 / antagonists & inhibitors
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2 / metabolism*
  • Calmodulin / metabolism*
  • Caspase 3 / metabolism
  • Cell Line
  • Cell Survival / drug effects
  • Cytochromes c / metabolism
  • Dose-Response Relationship, Drug
  • Endocrine Disruptors / toxicity*
  • Enzyme Activation
  • Male
  • Membrane Potential, Mitochondrial / drug effects
  • Mice
  • Mitochondria / drug effects
  • Mitochondria / enzymology
  • Mitochondria / pathology
  • Mitogen-Activated Protein Kinase 1 / antagonists & inhibitors
  • Mitogen-Activated Protein Kinase 1 / metabolism*
  • Mitogen-Activated Protein Kinase 3 / antagonists & inhibitors
  • Mitogen-Activated Protein Kinase 3 / metabolism*
  • Phenols / toxicity*
  • Phosphorylation
  • Protein Kinase Inhibitors / pharmacology
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Sertoli Cells / drug effects*
  • Sertoli Cells / enzymology
  • Sertoli Cells / pathology
  • Signal Transduction / drug effects
  • Time Factors

Substances

  • Benzhydryl Compounds
  • Calmodulin
  • Endocrine Disruptors
  • Phenols
  • Protein Kinase Inhibitors
  • Proto-Oncogene Proteins c-bcl-2
  • Cytochromes c
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2
  • Mapk1 protein, mouse
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3
  • Casp3 protein, mouse
  • Caspase 3
  • bisphenol A