Neurobiology Section, Biological Sciences Division, University of California San Diego, La Jolla, California, USA.
Nat Neurosci. 2010 Jan;13(1):29-35. doi: 10.1038/nn.2457. Epub 2009 Nov 29.
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.
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。