Serotonin 5-HT2A receptor induces TGF-beta 1 expression in mesangial cellsvia ERK: proliferative and fibrotic signals

Citation
Js. Grewal et al., Serotonin 5-HT2A receptor induces TGF-beta 1 expression in mesangial cellsvia ERK: proliferative and fibrotic signals, AM J P-REN, 45(6), 1999, pp. F922-F930
Citations number
46
Categorie Soggetti
da verificare
Journal title
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY
ISSN journal
03636127 → ACNP
Volume
45
Issue
6
Year of publication
1999
Pages
F922 - F930
Database
ISI
SICI code
0363-6127(199906)45:6<F922:S5RIT1>2.0.ZU;2-V
Abstract
We examined the links between fibrotic and proliferative pathways for the 5 -HT2A receptor in rat mesangial cells. Serotonin (5-hydroxytryptamine, 5-MT ) induced transforming growth factor-beta 1 (TGF-beta 1) mRNA in a concentr ation-dependent (peak at 30 nM 5-MT) and time-dependent fashion. For 10 nM 5-HT, the effect was noticeable at 1 h and maximal by 6 h. Inhibition of 1) protein kinase C (PKC), 2) mitogen- and extracellular signal-regulated kin ase kinase (MEK1) with 2'-amino-3'-methoxyflavone (PD-90859), and 3) extrac ellular signal-regulated kinase (ERK) with apigenin attenuated this effect. The effect was blocked by antioxidants, N-acetyl-L-cysteine (NAC) and cr-l ipoic acid, and mimicked by direct application of H2O2. TGF-beta 1 mRNA ind uction was also blocked by diphenyleneiodonium and 4-(2-aminoethyl)-benzene sulfonyl fluoride, which inhibit NAD(P)H oxidase, a source of oxidants. 5-H T increased the amount of TGF-P 1 protein, validating the mRNA studies and demonstrating that 5-HT potently activates ERK and induces TGF-beta 1 mRNA and protein in mesangial cells. Mapping studies strongly supported relative positions of the components of the signaling cascade as follow: 5-HT2A rec eptor --> PKC --> NAD(P)H oxidase/reactive oxygen species --> MEK --> ERK - -> TGF-beta 1 mRNA. These studies demonstrate that mitogenic signaling comp onents (PKC, MEK, and oxidants) are directly linked to the regulation of TG F-beta 1, a key mediator of fibrosis. Thus a single stimulus can direct bot h proliferative and fibrotic signals in renal mesangial cells.