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PMID: 17596297 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Requirement of Ca2+ influx- and phosphatidylinositol 3-kinase-mediated m-calpain activity for shear stress-induced endothelial cell polarity.

American journal of physiology. Cell physiology ·Vol. 293 ·No. 4 ·2007-10-00 ·Pages C1216-25

Miyazaki T, Honda K, Ohata H

Abstract

Proteolytic activity in sheared human umbilical vein endothelial cells (HUVECs) was measured using a fluorogenic substrate and laser scanning confocal microscopy to clarify the key role of an intracellular Ca(2+)-sensitive protease, calpain, in these cells in response to shear stress. Within physiological shear range, activity in the cells was enhanced in shear-dependent fashion. Short interfering RNA-induced silencing of m-calpain, but not of micro-calpain, suppressed the activity. Either removal of extracellular Ca(2+) or application of an intracellular Ca(2+) chelator (BAPTA/AM) or nonselective cation channel blocker (Gd(3+)) reduced proteolytic activity. Furthermore, activity was suppressed by phosphatidylinositol bisphosphate (PIP(2)) chelator (neomycin) or phosphatidylinositol 3-kinase (PI3K) inhibitor (LY294002); in contrast, activity, which was partially inhibited by ERK kinase inhibitor (U0126, PD98059), was unaffected by PLC inhibitor (U73122). Moreover, Akt phosphorylation downstream of PI3K, which was elicited by shear, was attenuated by neomycin but not by calpain inhibitor (calpeptin). Following assessment of shear stress-induced focal adhesion (FA) and cytoskeletal dynamics using interference reflection/green fluorescence protein-actin microscopy, we found that either calpain or PI3K inhibition impaired shear stress-induced polarization of FAs via stabilization of FA structures. Additionally, HUVEC alignment and cytoskeletal remodeling, which was accompanied by calpain-mediated cleavage of vinculin and talin, were also elicited by prolonged application of shear and impaired by m-calpain knockdown. Thus, these results revealed that physiological shear stress elicits Ca(2+) influx-sensitive activation of m-calpain in HUVECs. This activity is facilitated primarily through the PI3K pathway; furthermore, it is essential for subsequent FA reorganization and cell alignment under shear conditions.

MeSH Terms
Actins/metabolism Calcium/metabolism Calpain/antagonists & inhibitors,genetics,metabolism Cell Polarity/physiology Cells, Cultured Chromones/pharmacology Cytoskeleton/drug effects,metabolism Dipeptides/pharmacology Endothelial Cells/cytology,drug effects,metabolism Flavonoids/pharmacology Focal Adhesions/drug effects,metabolism Gadolinium/pharmacology Humans Microscopy, Confocal Morpholines/pharmacology Neomycin/pharmacology Phosphatidylinositol 3-Kinases/metabolism Phosphoinositide-3 Kinase Inhibitors Phosphorylation/drug effects Protein Kinase Inhibitors/pharmacology Proto-Oncogene Proteins c-akt/metabolism Pseudopodia/drug effects,metabolism RNA, Small Interfering/genetics Stress, Mechanical Talin/metabolism Vinculin/metabolism
Chemicals
Actins Chromones Dipeptides Flavonoids Morpholines Phosphoinositide-3 Kinase Inhibitors Protein Kinase Inhibitors RNA, Small Interfering Talin Vinculin calpeptin 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one Gadolinium Proto-Oncogene Proteins c-akt Calpain m-calpain Neomycin 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one Calcium
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Miyazaki Takuro
Department of Pharmacology, School of Pharmaceutical Sciences, Showa University, Tokyo, Japan. taku@pharm.showa-u.ac.jp
Honda Kazuo
Ohata Hisayuki
Article Info
Journal
American journal of physiology. Cell physiology
Abbr.
Am J Physiol Cell Physiol
ISSN
0363-6143
Published
2007-10-00
Epub
2007-00-27
Pages
C1216-25
Language
English
Region
United States
NLM ID
100901225
Subset
IM
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