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.