ARF6 and Rab11 as intrinsic regulators of axon regeneration.

Q2 Biochemistry, Genetics and Molecular Biology Small GTPases Pub Date : 2020-11-01 Epub Date: 2018-05-17 DOI:10.1080/21541248.2018.1457914
Bart Nieuwenhuis, Richard Eva
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Abstract

Adult central nervous system (CNS) axons do not regenerate after injury because of extrinsic inhibitory factors, and a low intrinsic capacity for axon growth. Developing CNS neurons have a better regenerative ability, but lose this with maturity. This mini-review summarises recent findings which suggest one reason for regenerative failure is the selective distribution of growth machinery away from axons as CNS neurons mature. These studies demonstrate roles for the small GTPases ARF6 and Rab11 as intrinsic regulators of polarised transport and axon regeneration. ARF6 activation prevents the axonal transport of integrins in Rab11 endosomes in mature CNS axons. Decreasing ARF6 activation permits axonal transport, and increases regenerative ability. The findings suggest new targets for promoting axon regeneration after CNS injury.

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ARF6和Rab11作为轴突再生的内在调节因子。
成人中枢神经系统(CNS)轴突在损伤后由于外源性抑制因素而不能再生,并且轴突生长的内在能力较低。发育中的中枢神经系统神经元具有较好的再生能力,但随着成熟而失去这种能力。这篇小型综述总结了最近的发现,这些发现表明再生失败的一个原因是随着中枢神经系统神经元成熟,生长机制选择性地分布在远离轴突的地方。这些研究证明了小GTPases ARF6和Rab11作为极化运输和轴突再生的内在调节因子的作用。ARF6激活可阻止成熟中枢神经系统轴突中Rab11内体整合素的轴突运输。ARF6激活的减少允许轴突运输,并增加再生能力。这一发现提示了促进中枢神经系统损伤后轴突再生的新靶点。
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来源期刊
Small GTPases
Small GTPases Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
6.10
自引率
0.00%
发文量
6
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