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Sonic hedgehog 诱导连合纤维在中线穿越过程中对 Semaphorin 排斥的反应。

Sonic hedgehog induces response of commissural axons to Semaphorin repulsion during midline crossing.

机构信息

Neurobiology Section, Biological Sciences Division, University of California San Diego, La Jolla, California, USA.

出版信息

Nat Neurosci. 2010 Jan;13(1):29-35. doi: 10.1038/nn.2457. Epub 2009 Nov 29.

Abstract

Pathfinding axons change responses to guidance cues at intermediate targets. During midline crossing, spinal cord commissural axons acquire responsiveness to class 3 Semaphorins and Slits, which regulate their floor plate exit and restrict their post-crossing trajectory into a longitudinal pathway. We found that Sonic Hedgehog (Shh) could activate the repulsive response of pre-crossing axons to Semaphorins. Blocking Shh function with a monoclonal antibody to Shh, 5E1, in 'open-book' explants or by expressing a dominant-negative form of Patched-1, Ptch1(Delta loop2), or a Smoothened (Smo) shRNA construct in commissural neurons resulted in severe guidance defects, including stalling and knotting inside the floor plate, recrossing, randomized anterior-posterior projection and overshooting after crossing, reminiscent of Neuropilin-2 mutant embryos. Enhancing protein kinase A activity in pre-crossing axons diminished Shh-induced Semaphorin repulsion and caused profound midline stalling and overshooting/wandering of post-crossing axons. Therefore, a morphogen, Shh, can act as a switch of axon guidance responses.

摘要

轴突在中间靶点改变对导向线索的反应。在中线穿越过程中,脊髓连合轴突获得对 3 类 Semaforins 和 Slits 的反应性,这调节它们离开基板,并限制它们在穿越后进入纵向途径的轨迹。我们发现 Sonic Hedgehog (Shh) 可以激活穿越前轴突对 Semaforins 的排斥反应。用 Shh 的单克隆抗体 5E1 在“开书”外植体中阻断 Shh 功能,或在连合神经元中表达显性负形式的 Patched-1、Ptch1(Delta loop2)或 Smoothened (Smo) shRNA 构建体,导致严重的导向缺陷,包括在基板内停滞和打结、重新穿越、穿越后前后投射随机化和过度穿越,类似于 Neuropilin-2 突变体胚胎。增强穿越前轴突中的蛋白激酶 A 活性会减弱 Shh 诱导的 Semaforin 排斥反应,并导致穿越后轴突严重的中线停滞和过度穿越/漫游。因此,形态发生素 Shh 可以作为轴突导向反应的开关。

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