Initiation of Oligodendrocyte Progenitor Cell Migration by a PDGF-A Activated Extracellular Regulated Kinase (ERK) Signaling Pathway

被引:70
作者
Frost, Emma E. [1 ,2 ]
Zhou, ZhiCheng [1 ,2 ]
Krasnesky, Kimberley [1 ,2 ]
Armstrong, Regina C. [3 ]
机构
[1] Univ Manitoba, Dept Pathol, Winnipeg, MB R3E 3P5, Canada
[2] Manitoba Inst Child Hlth, Winnipeg, MB, Canada
[3] Uniformed Serv Univ Hlth Sci, Dept Anat & Physiol & Genet, Bethesda, MD 20814 USA
基金
美国国家卫生研究院;
关键词
Oligodendrocyte progenitors; PDGF receptor; ERK signaling; Migration; PROTEIN-KINASE; SPINAL-CORD; PRECURSOR CELLS; GROWTH; PROLIFERATION; INHIBITOR; ASTROCYTES; NETRIN-1; DYNAMICS; PATTERNS;
D O I
10.1007/s11064-008-9748-z
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
During CNS development, oligodendrocyte progenitor (OP) cells migrate from germinal zones to presumptive white matter tracts to generate myelinating oligodendrocytes. In vitro and in vivo studies indicate that platelet-derived growth factor-A (PDGF-A) is a potent chemoattractant for OP cells and important for normal distribution throughout the developing CNS. However, PDGF-A does not localize in concentration gradients corresponding to OP migratory pathways, as would be expected for a chemoattractant to direct migration. Therefore, the mechanism by which PDGF-A regulates OP distribution remains to be clarified. Here we show that PDGF-A induces OP migration and continuous exposure to PDGF-A is not required to maintain migration. Using pharmacological inhibitors, we show that a self-sustaining extracellular-regulated-kinase signaling pathway drives OP migration for up to 72 hours after the initial PDGF stimulus. These findings indicate PDGF-A may act to mobilize OP cells that then respond to distinct directional signals to distribute appropriately within the CNS.
引用
收藏
页码:169 / 181
页数:13
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