Mitochondrial cAMP exerts positive feedback on mitochondrial Ca 2+ uptake via the recruitment of Epac1
We have previously demonstrated in H295R adrenocortical cells that the Ca -dependent production of mitochondrial cAMP (mt-cAMP) by the matrix soluble adenylyl cyclase (sAC; encoded by ) is associated with enhanced aldosterone production. Here, we examined whether mitochondrial sAC and mt-cAMP fine t...
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Published in | Journal of cell science Vol. 131; no. 10 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
England
16.05.2018
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Subjects | |
Online Access | Get full text |
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Summary: | We have previously demonstrated in H295R adrenocortical cells that the Ca
-dependent production of mitochondrial cAMP (mt-cAMP) by the matrix soluble adenylyl cyclase (sAC; encoded by
) is associated with enhanced aldosterone production. Here, we examined whether mitochondrial sAC and mt-cAMP fine tune mitochondrial Ca
metabolism to support steroidogenesis. Reduction of mt-cAMP formation resulted in decelerated mitochondrial Ca
accumulation in intact cells during K
-induced Ca
signalling and also in permeabilized cells exposed to elevated perimitochondrial [Ca
]. By contrast, treatment with the membrane-permeable cAMP analogue 8-Br-cAMP, inhibition of phosphodiesterase 2 and overexpression of sAC in the mitochondrial matrix all intensified Ca
uptake into the organelle. Identical mt-cAMP dependence of mitochondrial Ca
uptake was also observed in HeLa cells. Importantly, the enhancing effect of mt-cAMP on Ca
uptake was independent from both the mitochondrial membrane potential and Ca
efflux, but was reduced by Epac1 (also known as RAPGEF3) blockade both in intact and in permeabilized cells. Finally, overexpression of sAC in the mitochondrial matrix potentiated aldosterone production implying that the observed positive feedback mechanism of mt-cAMP on mitochondrial Ca
accumulation may have a role in the rapid initiation of steroidogenesis.This article has an associated First Person interview with the first author of the paper. |
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ISSN: | 1477-9137 |