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Cytosolic inositol 1,4,5-trisphosphate dynamics during intracellular calcium oscillations in living cells.


ABSTRACT: We developed genetically encoded fluorescent inositol 1,4,5-trisphosphate (IP3) sensors that do not severely interfere with intracellular Ca2+ dynamics and used them to monitor the spatiotemporal dynamics of both cytosolic IP3 and Ca2+ in single HeLa cells after stimulation of exogenously expressed metabotropic glutamate receptor 5a or endogenous histamine receptors. IP3 started to increase at a relatively constant rate before the pacemaker Ca2+ rise, and the subsequent abrupt Ca2+ rise was not accompanied by any acceleration in the rate of increase in IP3. Cytosolic [IP3] did not return to its basal level during the intervals between Ca2+ spikes, and IP3 gradually accumulated in the cytosol with a little or no fluctuations during cytosolic Ca2+ oscillations. These results indicate that the Ca2+ -induced regenerative IP3 production is not a driving force of the upstroke of Ca2+ spikes and that the apparent IP3 sensitivity for Ca2+ spike generation progressively decreases during Ca2+ oscillations.

SUBMITTER: Matsu-ura T 

PROVIDER: S-EPMC2063891 | biostudies-other | 2006 Jun

REPOSITORIES: biostudies-other

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Cytosolic inositol 1,4,5-trisphosphate dynamics during intracellular calcium oscillations in living cells.

Matsu-ura Toru T   Michikawa Takayuki T   Inoue Takafumi T   Miyawaki Atsushi A   Yoshida Manabu M   Mikoshiba Katsuhiko K  

The Journal of cell biology 20060601 5


We developed genetically encoded fluorescent inositol 1,4,5-trisphosphate (IP3) sensors that do not severely interfere with intracellular Ca2+ dynamics and used them to monitor the spatiotemporal dynamics of both cytosolic IP3 and Ca2+ in single HeLa cells after stimulation of exogenously expressed metabotropic glutamate receptor 5a or endogenous histamine receptors. IP3 started to increase at a relatively constant rate before the pacemaker Ca2+ rise, and the subsequent abrupt Ca2+ rise was not  ...[more]

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