Endothelin‐1 increases the expression of VEGF‐R1/Flt‐1 receptors in rat cultured astrocytes through ETB receptors. (8th July 2014)

• Record Type: Journal Article
• Authors: Koyama, Yutaka; Hayashi, Mio; Nagae, Ryuji; Tokuyama, Shogo; Konishi, Tomohiro
• Is Part Of: Journal of neurochemistry. Volume 130:Number 6(2014:Sep.)
• Page Start: 759
• Page End: 769
• Publication Date: 2014-07-08
• Subjects: Neurochemistry -- Periodicals; 616.8042
• DOI: 10.1111/jnc.12770
• Languages: English
• ISSNs: 0022-3042

Abstract

<abstract abstract-type="main" id="jnc12770-abs-0001"> <title>Abstract</title> <p>Expressions of vascular endothelial growth factor (VEGF) receptors in astrocytes are increased in damaged brains. To clarify the regulatory mechanisms of VEGF receptors, the effects of endothelin‐1 (ET‐1) were examined in rat cultured astrocytes. Expressions of VEGF‐R1 and ‐R2 receptor mRNA were at similar levels, whereas the mRNA expressions of VEGF‐R3 and Tie‐2, a receptor for angiopoietins, were lower. Placenta growth factor, a selective agonist of the VEGF‐R1 receptor, induced phosphorylation of focal adhesion kinase (FAK) and extracellular signal regulated kinase 1/2 (ERK1/2). Phosphorylations of FAK and ERK 1/2 were also stimulated by VEGF‐E, a selective VEGF‐R2 agonist. Increased phosphorylations of FAK and ERK1/2 by VEGF<sub>165</sub> were reduced by selective antagonists for VEGF‐R1 and ‐R2. Treatment with ET‐1 increased VEGF‐R1 mRNA and protein levels. The effects of ET‐1 on VEGF‐R1 mRNA were mimicked by Ala<sup>1, 3, 11, 15</sup>‐ET‐1, a selective agonist for ET<sub>B</sub> receptors, and inhibited by BQ788, an ET<sub>B</sub> antagonist. ET‐1 did not affect the mRNA levels of VEGF‐R2, ‐R3, and Tie‐2. Pre‐treatment with ET‐1 potentiated the effects of placenta growth factor on phosphorylations of FAK and ERK1/2. These findings suggest that ET‐1 induces up‐regulation of VEGF‐R1 receptors in astrocytes, and potentiates VEGF signals in damaged nerve tissues.</p> <p> <boxed-text content-type="graphic" id="jnc12770-blkfxd-1001" position="anchor" orientation="portrait"> <graphic position="anchor" mimetype="image" xlink:href="ark:/27927/pgh177kn9gc" orientation="portrait" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink" /> </boxed-text> To clarify the regulatory mechanisms of vascular endothelial growth factor (VEGF) receptors, the effects of endothelin‐1 (ET‐1) were examined in rat cultured astrocytes. Effects of selective VEGF‐R1 and R2 agonist showed that these receptors were linked to focal adhesion kinase (FAK) and extracellular signal regulated kinase 1/2 (ERK1/2). Treatment with ET‐1 increased expression of VEGF‐R1, which was mediated by ET<sub>B</sub> receptors. Pre‐treatment with ET‐1 potentiated the VEGF‐R1‐mediated activations of FAK and ERK1/2. These findings suggest that ET‐1 induces up‐regulation of VEGF‐R1 receptors in astrocytes.</p> </abstract>