Journal
JOURNAL OF NEUROSCIENCE RESEARCH
Volume 76, Issue 1, Pages 35-50Publisher
WILEY
DOI: 10.1002/jnr.20045
Keywords
neural progenitor cell; neurogenesis; SDF-1 alpha; CXCR4; intracellular signaling
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Funding
- NCRR NIH HHS [P20 RR15635-01] Funding Source: Medline
- NINDS NIH HHS [R01 NS41858-01, NS043958] Funding Source: Medline
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Stromal cell-derived factor 1 (SDF-1) and the chemokine receptor CXCR4 are highly expressed in the nervous system. Knockout studies have suggested that both SDF-1 and CXCR4 play essential roles in cerebellar, hippocampal, and neocortical neural cell migration during embryogenesis. To extend these observations, CXCR4 signaling events in rat and human neural progenitor cells (NPCs) were examined. Our results show that CXCR4 is expressed in abundance on rat and human NPCs. Moreover, SDF-1alpha induced increased NPCs levels of inositol 1,4,5-triphosphate, extracellular signal-regulated kinases 1/2, Akt, c-Jun N-terminal kinase, and intracellular calcium whereas it diminished cyclic adenosine monophosphate. Finally, SDF-1alpha can induce human NPC chemotaxis in vitro, suggesting that CXCR4 plays a functional role in NPC migration. Both T140, a CXCR4 antagonist, and pertussis toxin (PTX), an inactivator of G protein-coupled receptors, abrogated these events. Ultimately, this study suggested that SDF-1alpha can influence NPC function through CXCR4 and that CXCR4 is functional on NPC. (C) 2004 Wiley-Liss, Inc.
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