Mitochondrial Ca uptake with and without the formation of high-Ca microdomains |
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Authors: | Gerg Szanda, P ter Koncz, P ter V rnai,Andr s Sp t |
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Affiliation: | aDepartment of Physiology, Faculty of Medicine, Semmelweis University and Laboratory of Cellular and Molecular Physiology, Hungarian Academy of Sciences, P.O. Box 259, H-1444 Budapest, Hungary |
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Abstract: | The mitochondrial Ca2+ uniporter has low affinity for Ca2+, therefore it has been assumed that submicromolar Ca2+ signals cannot induce mitochondrial Ca2+ uptake. The close apposition of the plasma membrane or the endoplamic reticulum (ER) to the mitochondria and the limited Ca2+ diffusion in the cytoplasm result in the formation of perimitochondrial high-Ca2+ microdomains (HCMDs) capable of activating mitochondrial Ca2+ uptake. The possibility of mitochondrial Ca2+ uptake at low submicromolar [Ca2+]c has not yet been generally accepted.Earlier we found in permeabilized glomerulosa, luteal and pancreatic β cells that [Ca2+]m increased when [Ca2+]c was raised from 60 nM to less than 200 nM. Here we report data obtained from H295R (adrenocortical) cells transfected with ER-targeted GFP. Cytoplasmic Ca2+ response to angiotensin II was different in mitochondrion-rich and mitochondrion-free domains. The mitochondrial Ca2+ response to angiotensin II correlated with GFP fluorescence indicating the vicinity of ER. When the cells were exposed to K+ (inducing Ca2+ influx), no correlation was found between the mitochondrial Ca2+ signal and the vicinity of the plasma membrane or the ER. The results presented here provide evidence that mitochondrial Ca2+ uptake may occur both with and without the formation of HCMDs within the same cell. |
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Keywords: | Ca2+ signal Mitochondria Endoplasmic reticulum Glomerulosa cell H295R cells Angiotensin II Potassium Microdomains |
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