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Morphological profile determines the frequency of spontaneous calcium events in astrocytic processes
Author(s) -
Wu YuWei,
Gordleeva Susan,
Tang Xiaofang,
Shih PeiYu,
Dembitskaya Yulia,
Semyanov Alexey
Publication year - 2019
Publication title -
glia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.954
H-Index - 164
eISSN - 1098-1136
pISSN - 0894-1491
DOI - 10.1002/glia.23537
Subject(s) - biology , extracellular , astrocyte , depolarization , calcium signaling , hippocampal formation , intracellular , microbiology and biotechnology , neuroscience , biophysics , inositol trisphosphate , calcium , neuroglia , receptor , inositol , biochemistry , central nervous system , chemistry , organic chemistry
Astrocytes express a complex repertoire of intracellular Ca 2+ transients (events) that represent a major form of signaling within individual cells and in astrocytic syncytium. These events have different spatiotemporal profiles, which are modulated by neuronal activity. Spontaneous Ca 2+ events appear more frequently in distal astrocytic processes and independently from each other. However, little is known about the mechanisms underlying such subcellular distribution of the Ca 2+ events. Here, we identify the initiation points of the Ca 2+ events within the territory of single astrocytes expressing genetically encoded Ca 2+ indicator GCaMP2 in culture or in hippocampal slices. We found that most of the Ca 2+ events start in an optimal range of thin distal processes. Our mathematical model demonstrated that a high surface‐to‐volume of the thin processes leads to increased amplitude of baseline Ca 2+ fluctuations caused by a stochastic opening of Ca 2+ channels in the plasma membrane. Suprathreshold fluctuations trigger Ca 2+ ‐induced Ca 2+ release from the Ca 2+ stores by activating inositol 1,4,5‐trisphosphate (IP 3 ) receptors. In agreement with the model prediction, the spontaneous Ca 2+ events frequency depended on the extracellular Ca 2+ concentration. Astrocytic depolarization by high extracellular K + increased the frequency of the Ca 2+ events through activation of voltage‐gated Ca 2+ channels in cultured astrocytes. Our results suggest that the morphological profile of the astrocytic processes is responsible for tuning of the Ca 2+ events frequency. Therefore, structural plasticity of astrocytic processes can be directly translated into changes in astrocytic Ca 2+ signaling. This may be important for both physiological and pathological astrocyte remodeling.