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Cloning of cDNAs Encoding G Protein-Coupled Receptor Expressed in Human Endothelial Cells Exposed to Fluid Shear Stress

https://doi.org/10.1006/bbrc.1997.7734Get rights and content

Abstract

A cDNA library of human umbilical vein endothelial cells exposed to fluid shear stress was constructed to search for functional endothelial genes expressed under flow conditions, and cDNAs encoding members of the G protein-coupled receptor (GPCR) family were cloned by a polymerase chain reaction (PCR) method using degenerate oligonucleotide primers. One of the two GPCR clones obtained was edg-1, and the other clone is a novel gene named FEG-1 that encodes a 375-amino acid protein similar to the receptors for both angiotensin II and chemokines. Reverse transcriptase-PCR showed that the FEG-1 and edg-1 mRNA levels in endothelial cells increased markedly in response to fluid flow. This suggests that FEG-1 and edg-1 may be receptor genes that play important roles in the regulation of endothelial function under physiological blood flow conditions.

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    Citation Excerpt :

    Moreover, while endothelial S1PR1 has been implicated as mechanosensitive to LSS in promoting vessel stabilization [36], our findings suggest a novel mechanosensitive role for S1PR1 in response to BFF along with S1PR2 in response to BFF and LSS in coordinating endothelial barrier function. Blood flow (i.e., LSS) enhances transcription and expression of S1PR1 [34, 36], and there is evidence of ligand independent activation of S1PR1 that leads to vessel stabilization [36]. However, there are no previous reports that address whether BFF elicits ligand independent activation of S1PR1.

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To whom correspondence should be addressed at Institute for Life Science Research, Asahi Chemical Industry Co., Ltd., 2-1, Samejima, Fuji-City, Shizuoka, 416 Japan. Fax: +81-545-62-3329. E-mail: [email protected].

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