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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Journal of Cellular ...arrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Journal of Cellular Physiology
Article . 2002 . Peer-reviewed
License: Wiley Online Library User Agreement
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Puromycin insensitive leucyl‐specific aminopeptidase (PILSAP) is involved in the activation of endothelial integrins

Authors: Tetsuya, Akada; Tohru, Yamazaki; Hiroki, Miyashita; Osamu, Niizeki; Mayumi, Abe; Akira, Sato; Susumu, Satomi; +1 Authors

Puromycin insensitive leucyl‐specific aminopeptidase (PILSAP) is involved in the activation of endothelial integrins

Abstract

AbstractWe previously reported that mouse orthologue of puromycin insensitive leucyl‐specific aminopeptidase (mPILSAP) played an important role in angiogenesis by regulating the proliferation and migration of endothelial cells (ECs) (Miyashita et al., 2002. Blood 99:3241–3249). Here, we examined the mechanism as to how mPILSAP regulates the migration of ECs. Cell adhesion through integrins plays a crucial role in cell migration, and ECs use at least type‐1 collagen receptor integrin α2β1, fibronectin receptor α5β1, and vitronectin receptors αvβ3 and αvβ5. mPILSAP antisense oligodeoxynucleotide (AS‐ODN) or leucinethiol (LT), a leucyl‐aminopeptidase inhibitor, did not affect the attachment but did significantly inhibit the spreading of cells of the murine endothelial cell line MSS31 when they were plated on vitronectin‐, fibronectin‐, or type‐1 collagen, although they did not affect the expression of integrin α2, α5, αv, β1, β3, and β5 subunits on the cell surface. AS‐ODN and LT also inhibited the tyrosine phosphorylation of FAK when cells were plated on vitronectin, fibronectin, or type‐1 collagen. This inhibition of cell spreading and of tyrosine phosphorylation of FAK could be negated by Mg2+. These results suggest that mPILSAP is involved in the activation of endothelial integrins. © 2002 Wiley‐Liss, Inc.

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Keywords

Protein Synthesis Inhibitors, Integrins, Oligonucleotides, Antisense, Extracellular Matrix, Androstadienes, Leucyl Aminopeptidase, Mice, Cell Movement, Leucine, Focal Adhesion Kinase 1, Focal Adhesion Protein-Tyrosine Kinases, Animals, Magnesium, Endothelium, Vascular, Enzyme Inhibitors, Phosphorylation, Cell Adhesion Molecules, Cells, Cultured, Cell Line, Transformed, Phosphoinositide-3 Kinase Inhibitors

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
35
Average
Top 10%
Top 10%
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