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Red fluorescent CEPIA indicators for visualization of Ca2+ dynamics in mitochondria.


ABSTRACT: Mitochondrial Ca2+ dynamics are involved in the regulation of multifarious cellular processes, including intracellular Ca2+ signalling, cell metabolism and cell death. Use of mitochondria-targeted genetically encoded Ca2+ indicators has revealed intercellular and subcellular heterogeneity of mitochondrial Ca2+ dynamics, which are assumed to be determined by distinct thresholds of Ca2+ increases at each subcellular mitochondrial domain. The balance between Ca2+ influx through the mitochondrial calcium uniporter and extrusion by cation exchangers across the inner mitochondrial membrane may define the threshold; however, the precise mechanisms remain to be further explored. We here report the new red fluorescent genetically encoded Ca2+ indicators, R-CEPIA3mt and R-CEPIA4mt, which are targeted to mitochondria and their Ca2+ affinities are engineered to match the intramitochondrial Ca2+ concentrations. They enable visualization of mitochondrial Ca2+ dynamics with high spatiotemporal resolution in parallel with the use of green fluorescent probes and optogenetic tools. Thus, R-CEPIA3mt and R-CEPIA4mt are expected to be a useful tool for elucidating the mechanisms of the complex mitochondrial Ca2+ dynamics and their functions.

SUBMITTER: Kanemaru K 

PROVIDER: S-EPMC7029041 | biostudies-literature | 2020 Feb

REPOSITORIES: biostudies-literature

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Red fluorescent CEPIA indicators for visualization of Ca<sup>2+</sup> dynamics in mitochondria.

Kanemaru Kazunori K   Suzuki Junji J   Taiko Isamu I   Iino Masamitsu M  

Scientific reports 20200218 1


Mitochondrial Ca<sup>2+</sup> dynamics are involved in the regulation of multifarious cellular processes, including intracellular Ca<sup>2+</sup> signalling, cell metabolism and cell death. Use of mitochondria-targeted genetically encoded Ca<sup>2+</sup> indicators has revealed intercellular and subcellular heterogeneity of mitochondrial Ca<sup>2+</sup> dynamics, which are assumed to be determined by distinct thresholds of Ca<sup>2+</sup> increases at each subcellular mitochondrial domain. The b  ...[more]

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