Lysophosphatidylcholine enhances NGF‐induced MAPK and Akt signals through the extracellular domain of TrkA in PC12 cells. Issue 1 (30th May 2013)

• Record Type: Journal Article
• Authors: Wuhanqimuge, ; Itakura, Asako; Matsuki, Yuri; Tanaka, Masato; Arioka, Manabu
• Is Part Of: FEBS open bio. Volume 3:Issue 1(2013)
• Page Start: 243
• Page End: 251
• Publication Date: 2013-05-30
• Subjects: Akt -- Lysophosphatidylcholine -- Mitogen-activated protein kinase (MAPK) -- Nerve growth factor -- TrkA; Molecular biology -- Periodicals; Cytology -- Periodicals; Life sciences -- Periodicals; Biological Science Disciplines -- Periodicals; Molecular Biology -- Periodicals; Cell Biology -- Periodicals; Cytology; Life sciences; Molecular biology; Periodicals; 572.805
• DOI: 10.1016/j.fob.2013.05.003
• Languages: English
• ISSNs: 2211-5463

Abstract

Abstract : Lysophosphatidylcholine (LPC) is one of the major lysophospholipids mainly generated by phospholipase A2 (PLA2 )‐mediated hydrolysis of phosphatidylcholine (PC). We previously found that LPC displays neurotrophin‐like activity in the rat pheochromocytoma PC12 cells and in cerebellar granule neurons, but the molecular mechanism remains unclear. We report here that LPC specifically enhances nerve growth factor (NGF)‐induced signals in PC12 cells. When PC12 cells were treated with NGF, MAPK was phosphorylated, but this phosphorylation was significantly elevated when LPC was added together. In accordance, NGF‐induced expression of immediate early genes, c‐ fos and NGF‐IA, was upregulated by LPC. Phosphorylation of the upstream components, MEK and NGF receptor TrkA, was also promoted by LPC, which was in line with increased phosphorylation of Akt. In contrast, LPC did not enhance epidermal growth factor (EGF)‐, basic fibroblast growth factor‐, or insulin‐like growth factor‐1‐induced signals. Studies using TrkA/EGF receptor chimeras demonstrated that the extracellular domain, but not the transmembrane or intracellular domains, of TrkA is responsible for the effect of LPC. Exogenously‐added secretory PLA2 (sPLA2 ) enhanced NGF‐induced MAPK phosphorylation at a comparable level to LPC, suggesting that LPC generated in situ by sPLA2 ‐mediated hydrolysis of membrane PC stimulated NGF‐TrkA signal. Taken together, these results indicate a specific role and function of LPC on NGF‐TrkA signaling pathway. Abstract : LPC potentiates NGF‐induced MAPK and Akt phosphorylation in PC12 cells. LPC enhances NGF‐induced MEK and TrkA phosphorylation. LPC does not affect the signals of EGF, FGF, and IGF‐1. The effect of LPC requires the extracellular domain of TrkA. sPLA2 also potentiates NGF‐induced MAPK phosphorylation.