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PMID: 2372294 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Shear stress increases inositol trisphosphate levels in human endothelial cells.

Biochemical and biophysical research communications ·Vol. 170 ·No. 1 ·1990-07-16 ·Pages 281-7

Nollert MU, Eskin SG, McIntire LV

Abstract

To elucidate some of the early mechanisms underlying the response of primary human endothelial cells to the initiation of flow, we investigated the changes in inositol lipid metabolism in cells exposed to arterial and venous levels of shear stress. We used a radioimmunoassay specific for inositol-1,4,5-trisphosphate (Ins1,4,5P3) to demonstrate that initiation of an arterial shear stress caused a rapid rise in Ins1,4,5P3 levels which peaked after approximately 30 seconds of flow (2.1 +/- 0.2 fold stimulation) and remained elevated for at least 6 minutes after the initiation of flow. This increased Ins1,4,5P3 concentration is similar in magnitude to the increase caused by 10 microM histamine (2.8 +/- 0.3 fold stimulation). Thus these cells may detect the presence of mechanical stress by a signal transduction pathway involving inositol lipid metabolism.

MeSH Terms
Cells, Cultured Endothelium, Vascular/drug effects,metabolism Histamine/pharmacology Humans Inositol 1,4,5-Trisphosphate/metabolism Second Messenger Systems Signal Transduction/physiology Stimulation, Chemical Stress, Mechanical
Chemicals
Histamine Inositol 1,4,5-Trisphosphate
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Nollert M U
Biomedical Engineering Laboratory, Rice University, Houston, TX 77251.
Eskin S G
McIntire L V
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
1990-07-16
Pages
281-7
Language
English
Region
United States
NLM ID
0372516
Subset
IM
Grants
NHLBI NIH HHS · HL-17437 · United States
NHLBI NIH HHS · HL-18762 · United States
NINDS NIH HHS · NS-18494 · United States
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