TGF-β Signaling Specifies Axons during Brain Development

被引:224
作者
Yi, Jason J. [1 ,2 ]
Barnes, Anthony P. [4 ]
Hand, Randal [4 ]
Polleux, Franck [4 ]
Ehlers, Michael D. [1 ,2 ,3 ]
机构
[1] Duke Univ, Med Ctr, Dept Neurobiol, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA
[3] Duke Univ, Med Ctr, Howard Hughes Med Inst, Durham, NC 27710 USA
[4] Univ N Carolina, Dept Pharmacol, Ctr Neurosci, Chapel Hill, NC 27599 USA
关键词
GROWTH-FACTOR-BETA; POLARITY PROTEIN PAR6; TRANSFORMING GROWTH-FACTOR-BETA-1; TARGETED DISRUPTION; NEUROTROPHIC FACTOR; NERVOUS-SYSTEM; CELL-POLARITY; RECEPTOR; NEURONS; EXPRESSION;
D O I
10.1016/j.cell.2010.06.010
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
In the mammalian brain, the specification of a single axon and multiple dendrites occurs early in the differentiation of most neuron types. Numerous intracellular signaling events for axon specification have been described in detail. However, the identity of the extracellular factor(s) that initiate neuronal polarity in vivo is unknown. Here, we report that transforming growth factor beta (TGF-beta) initiates signaling pathways both in vivo and in vitro to fate naive neurites into axons. Neocortical neurons lacking the type II TGF-beta receptor (T beta R2) fail to initiate axons during development. Exogenous TGF-beta is sufficient to direct the rapid growth and differentiation of an axon, and genetic enhancement of receptor activity promotes the formation of multiple axons. Finally, we show that the bulk of these TGF-beta-dependent events are mediated by site-specific phosphorylation of Par6. These results define an extrinsic cue for neuronal polarity in vivo that patterns neural circuits in the developing brain.
引用
收藏
页码:144 / 157
页数:14
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