Hypergravity affects cell cycle progression and caveolin-1 expression of in vitro cultured human primary endothelial cells

Santi, S.; Bianco, M.C.; Blasi, F.; Spisni, E.; Riccio, M.; Toni, M.; Griffoni, C.; Tomasi, V.

Journal of Gravitational Physiology a Journal of the International Society for Gravitational Physiology 9(1): P283-P284

2002


ISSN/ISBN: 1077-9248
PMID: 15002582
Document Number: 551958
In hypogravity conditions unloading of skeletal muscle fibres causes alterations in skeletal muscle structure and functions including growth, gene expression, cell differentiation, cytoskeletal organization, contractility and plasticity. Recent studies have identified sphingosine I -phosphate (SPP) as a lipid mediator capable of eliciting intracellular Ca2+ transients, cell proliferation, differentiation, suppression of apoptosis, as well as cell injury repair. The aim of this research is to evaluate a possible involvement of SPP in skeletal muscle cells differentiation and repair from space-flight damage. Particularly, we investigated the Ca2+ sources and the changes on the cytoskeletal rearrangement induced by SPP in a mouse skeletal (C2C12) myoblastic cell line. Confocal fluorescence imaging revealed that SPP elicited Ca2+ transients which propagated throughout the cytosol and nucleus. This response required extracellular and intracellular Ca2+ mobilization. SPP also induced cell contraction through a Ca2(+)- independent/Rho-dependent pathway. The nuclear Ca2+ transients are suggestive for an action of SPP in the differentiation program and damage repair.

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