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Ca2+ Entry is Required for Mechanical Stimulation-induced ATP Release from Astrocyte

Authors
Lee, JaekwangChun, Ye-EunHan, Kyung-SeokLee, JungmooWoo, Dong HoLee, C. Justin
Issue Date
Mar-2015
Publisher
KOREAN SOC BRAIN & NEURAL SCIENCE, KOREAN SOC NEURODEGENERATIVE DISEASE
Keywords
Astrocytes; ATP; Mechanical stimulation; Ca2+
Citation
EXPERIMENTAL NEUROBIOLOGY, v.24, no.1, pp.17 - 23
Indexed
KCI
Journal Title
EXPERIMENTAL NEUROBIOLOGY
Volume
24
Number
1
Start Page
17
End Page
23
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/94186
DOI
10.5607/en.2015.24.1.17
ISSN
1226-2560
Abstract
Astrocytes and neurons are inseparable partners in the brain. Neurotransmitters released from neurons activate corresponding G protein-coupled receptors (GPCR) expressed in astrocytes, resulting in release of gliotransmitters such as glutamate, D-serine, and ATP. These gliotransmitters in turn influence neuronal excitability and synaptic activities. Among these gliotransmitters, ATP regulates the level of network excitability and is critically involved in sleep homeostasis and astrocytic Ca2+ oscillations. ATP is known to be released from astrocytes by Ca2+- dependent manner. However, the precise source of Ca2+, whether it is Ca2+ entry from outside of cell or from the intracellular store, is still not clear yet. Here, we performed sniffer patch to detect ATP release from astrocyte by using various stimulation. We found that ATP was not released from astrocyte when Ca2+ was released from intracellular stores by activation of G alpha(q)- coupled GPCR including PAR1, P2YR, and B2R. More importantly, mechanical stimulation (MS)induced ATP release from astrocyte was eliminated when external Ca2+ was omitted. Our results suggest that Ca2+ entry, but not release from intracellular Ca2+ store, is critical for MS-induced ATP release from astrocyte.
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