PMID- 14635227 OWN - NLM STAT- MEDLINE DCOM- 20040108 LR - 20101118 IS - 0360-4012 (Print) IS - 0360-4012 (Linking) VI - 74 IP - 5 DP - 2003 Dec 1 TI - Hepatocyte growth factor stimulates cell motility in cultures of the striatal progenitor cells ST14A. PG - 760-8 AB - Hepatocyte growth factor/scatter factor (HGF/SF) is a growth factor with pleiotropic effects on different cell types. It acts as a mitogen and motility factor for many epithelial cells. HGF/SF and its receptor Met are present in the developing and adult mammalian brain and control neuritogenesis of sympathetic and sensory neurons. We report that the striatal progenitor ST14A cells express the Met receptor, which is activated after binding with HGF/SF. The interaction between Met and HGF/SF triggers a signaling cascade that leads to increased levels of c-Jun, c-Fos, and Egr-1 proteins, in agreement with data reported on the signaling events evoked by HGF in other cellular types. We also studied the effects of the exposure of ST14A cells to HGF/SF. By time-lapse photography, we observed that a 24-hr treatment with 50 ng/ml HGF/SF induced modification in cell morphology, with a decrease in cell-cell interactions and increase of cell motility. In contrast, no effect on cell proliferation was observed. To investigate which intracellular pathway is primarily involved we used PD98059 and LY294002, two specific inhibitors of mitogen-activated protein kinase/extracellular signal-regulated kinase (MAP-kinase/ERK-kinase) and phosphoinositide 3-OH kinase (PI3-K), respectively. Cell motility in HGF/SF treated cultures was inhibited by LY294002 but not by PD98059, suggesting that PI3-K plays a key role in mediating the HGF/SF-induced dissociation of ST14A cells. Previous evidence of HGF stimulation of motility in nervous system has been obtained on postmitotic neurons, which have already acquired their specificity. Data reported here of a motogenic response of ST14A cell line, which displays properties of neuronal progenitors, seem of interest because they suggest that HGF could play a role in very early steps of neurogenesis. CI - Copyright 2003 Wiley-Liss, Inc. FAU - Cacci, E AU - Cacci E AD - Dipartimento di Biologia Cellulare e dello Sviluppo, Universita La Sapienza, Roma, Italy. FAU - Salani, M AU - Salani M FAU - Anastasi, S AU - Anastasi S FAU - Perroteau, I AU - Perroteau I FAU - Poiana, G AU - Poiana G FAU - Biagioni, S AU - Biagioni S FAU - Augusti-Tocco, G AU - Augusti-Tocco G LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - J Neurosci Res JT - Journal of neuroscience research JID - 7600111 RN - 67256-21-7 (Hepatocyte Growth Factor) RN - EC 2.7.1.- (Phosphatidylinositol 3-Kinases) RN - EC 2.7.10.1 (Proto-Oncogene Proteins c-met) RN - EC 2.7.12.2 (Mitogen-Activated Protein Kinase Kinases) SB - IM MH - Animals MH - Blotting, Western MH - Cell Communication/drug effects MH - Cell Division/drug effects MH - Cell Line MH - Cell Movement/*drug effects MH - Corpus Striatum/cytology/drug effects/embryology MH - Embryo, Mammalian MH - Genes, Immediate-Early/drug effects MH - Hepatocyte Growth Factor/*pharmacology MH - Immunohistochemistry MH - Mice MH - Mitogen-Activated Protein Kinase Kinases/metabolism MH - Neurons/*drug effects/physiology MH - Phosphatidylinositol 3-Kinases/metabolism MH - Precipitin Tests MH - Proto-Oncogene Proteins c-met/*physiology MH - Rats MH - Stem Cells/*drug effects/physiology EDAT- 2003/11/25 05:00 MHDA- 2004/01/09 05:00 CRDT- 2003/11/25 05:00 PHST- 2003/11/25 05:00 [pubmed] PHST- 2004/01/09 05:00 [medline] PHST- 2003/11/25 05:00 [entrez] AID - 10.1002/jnr.10799 [doi] PST - ppublish SO - J Neurosci Res. 2003 Dec 1;74(5):760-8. doi: 10.1002/jnr.10799.