Abstract

Large-conductance calcium and voltage-dependent potassium (BK Ca) channel is an important determinant of vascular tone. It is activated by hydrogen peroxide (H 2O 2) which occurs in various physiological and pathological processes. However, the regulation mechanism is not fully understood. In the present study, the mSlo in the presence or absence of hβ1 were cotransfected with the PTEN wt, PTEN C124S, PTEN G129E in HEK 293 cells. Typical BK Ca channel currents could be recorded in cell-attached configurations. We found that PTEN wt reduced the H 2O 2-induced BK Ca channel activation during the initial 10 min treatment. In contrast, coexpression with catalytically inactive PTEN C124S/PTEN G129E mutants that lack lipid phosphatase activity produced no regulation on the H 2O 2-induced BK Ca channel activation. These results demonstrated that PTEN regulated the H 2O 2-induced BK Ca channel activation through phosphatidylinositol 3-phosphatse. However, the inhibitory effect of PTEN on the H 2O 2-induced BK Ca channel activation was attenuated when cells were treated with H 2O 2 at concentrations higher than 100 μM or at 100 μM for long-term treatment. In addition, the p-AKT expression level in PTEN wt overexpressing cells was lower than that in control cells, and the increase of cytoplasmic free calcium concentration ([Ca 2+] i) induced by H 2O 2 was also inhibited. These findings may elucidate a new mechanism for H 2O 2-induced BK Ca channel activation and provide some evidences for the role of PTEN on vasodilation induced by H 2O 2.

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