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Reelin, Rap1 and N-cadherin orient the migration of multipolar neurons in the developing neocortex
被引:266
作者:

Jossin, Yves
论文数: 0 引用数: 0
h-index: 0
机构:
Fred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98104 USA Fred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98104 USA

Cooper, Jonathan A.
论文数: 0 引用数: 0
h-index: 0
机构:
Fred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98104 USA Fred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98104 USA
机构:
[1] Fred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98104 USA
基金:
美国国家卫生研究院;
关键词:
CELL-CELL ADHESION;
CEREBRAL-CORTEX;
CORTICAL-NEURONS;
RADIAL MIGRATION;
INTERCELLULAR-JUNCTIONS;
LAMINAR ORGANIZATION;
SMALL GTPASES;
MOUSE-BRAIN;
ACTIVATION;
POLARITY;
D O I:
10.1038/nn.2816
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Projection neurons migrate from the ventricular zone to the neocortical plate during the development of the mouse brain. Their overall movement is radial, but they become multipolar and move nonradially in the intermediate zone. Here we show that Reelin, the Rap1 GTPase and N-cadherin (NCad) are important for multipolar neurons to polarize their migration toward the cortical plate. Inhibition and rescue experiments indicated that Reelin regulates migration through Rap1 and Akt, and that the Rap1-regulated GTPases RalA, RalB, Rac1 and Cdc42 are also involved. We found that Rap1 regulated the plasma membrane localization of NCad and NCad rescued radial polarization when Rap1 was inhibited. However, inhibition of Rap1 or NCad had little effect on glia-dependent locomotion. We propose a multistep mechanism in which Reelin activates Rap1, Rap1 upregulates NCad, and NCad is needed to orient cell migration.
引用
收藏
页码:697 / U289
页数:8
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