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Alterations of calcium homoeostasis in cultured rat astrocytes evoked by bioactive sphingolipids
Author(s) -
Stenovec M.,
Trkov S.,
Kreft M.,
Zorec R.
Publication year - 2014
Publication title -
acta physiologica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.591
H-Index - 116
eISSN - 1748-1716
pISSN - 1748-1708
DOI - 10.1111/apha.12314
Subject(s) - microbiology and biotechnology , extracellular , sphingolipid , purinergic receptor , sphingosine , calcium , biology , exocytosis , calcium signaling , vesicle , homeostasis , chemistry , biochemistry , intracellular , receptor , secretion , organic chemistry , membrane
Aim In the brain, alterations in sphingolipid metabolism contribute to several neurological disorders; however, their effect on astrocytes is largely unknown. Here, we identified bioactive sphingolipids that affect intracellular free calcium concentration ([Ca 2+ ] i ), mobility of peptidergic secretory vesicles, signalling pathways involved in alterations of calcium homoeostasis and explored the relationship between the stimulus‐evoked increase in [Ca 2+ ] i and attenuation of vesicle mobility. Methods Confocal time‐lapse images were acquired to explore [Ca 2+ ] i signals, the mobility of fluorescently tagged peptidergic vesicles and the structural integrity of the microtubules and actin filaments before and after the addition of exogenous sphingolipids to astrocytes. Results Fingolimod ( FTY 720), a recently introduced therapeutic for multiple sclerosis, and sphingosine, a releasable constituent of membrane sphingolipids, evoked long‐lasting increases in [Ca 2+ ] i in the presence and absence of extracellular Ca 2+ ; the evoked responses were diminished in the absence of extracellular Ca 2+ . Activation of phospholipase C and inositol‐1,4,5‐triphosphate receptors was necessary and sufficient to evoke increases in [Ca 2+ ] i as revealed by the pharmacologic inhibitors; Ca 2+ flux from the extracellular space intensified these responses several fold. The lipid‐evoked increases in [Ca 2+ ] i coincided with the attenuated vesicle mobility. High and positive correlation between increase in [Ca 2+ ] i and decrease in peptidergic vesicle mobility was confirmed independently in astrocytes exposed to evoked, transient Ca 2+ signalling triggered by purinergic and glutamatergic stimulation. Conclusion Exogenously added cell‐permeable sphingosine‐like lipids exert complex, Ca 2+ ‐dependent effects on astrocytes and likely alter their homeostatic function in vivo .