首页> 外文期刊>The Journal of Comparative Neurology >Involvement of sonic hedgehog and notch signaling in regenerative neurogenesis in adult zebrafish optic tectum after stab injury
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Involvement of sonic hedgehog and notch signaling in regenerative neurogenesis in adult zebrafish optic tectum after stab injury

机译:Sonic Hedgehog和Notch信号传导在刺伤后成人斑马鱼视色调中的再生神经发生中的参与

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Abstract Unlike humans and other mammals, adult zebrafish have the superior capability to recover from central nervous system (CNS) injury. We previously found that proliferation of radial glia (RG) is induced in response to stab injury in optic tectum and that new neurons are generated from RG after stab injury. However, molecular mechanisms which regulate proliferation and differentiation of RG are not well known. In the present study, we investigated Shh and Notch signaling as potential mechanisms regulating regeneration in the optic tectum of adult zebrafish. We used Shh reporter fish and confirmed that canonical Shh signaling is activated specifically in RG after stab injury. Moreover, we have shown that Shh signaling promotes RG proliferation and suppresses their differentiation into neurons after stab injury. In contrast, Notch signaling was down‐regulated after stab injury, indicated by the decrease in the expression level of her4 and her6 , a target gene of Notch signaling. We also found that inhibition of Notch signaling after stab injury induced more proliferative RG, but that inhibition of Notch signaling inhibited generation of newborn neurons from RG after stab injury. These results suggest that high level of Notch signaling keeps RG quiescent and that appropriate level of Notch signaling is required for generation of newborn neurons from RG. Under physiological condition, activation of Shh signaling or inhibition of Notch signaling also induced RG proliferation. In adult optic tectum of zebrafish, canonical Shh signaling and Notch signaling play important roles in proliferation and differentiation of RG in physiological and regenerative conditions.
机译:摘要与人类和其他哺乳动物不同,成人斑马鱼具有优异的能力,从中枢神经系统(CNS)受伤。我们以前发现桡曲胶质胶质增殖(RG)响应于视光图刺伤的抗刺伤,并且新神经元由抗损伤后的RG产生。然而,调节RG的增殖和分化的分子机制是不公知的。在本研究中,我们研究了SHH和NOTCH信号,作为调节成人斑马鱼视神经内的再生的潜在机制。我们使用SHH记者鱼并确认规范SHH信号传导在抗损伤后特别地在RG中激活。此外,我们已经表明,SHH信号传导促进RG增殖并在抗损伤后抑制它们的分化为神经元。相比之下,抗损伤后的Notch信号传导在抗损伤后下调,由HER4和HER6的表达水平降低,陷波信号传导的靶基因。我们还发现,抗损伤后缺口信号传导诱导更增殖的RG,但抑制抗损伤后缺口的Notch信号传导抑制新生神经元的产生。这些结果表明,高水平的陷波信号传导使RG静止,并且需要适当的缺口信号传导,从RG产生新生神经元。在生理条件下,SHH信号传导的激活或缺口信号传导的抑制也诱导RG增殖。在斑马鱼的成人视光图中,规范SHH信号和Notch信号传导在生理和再生条件下的增殖和分化中起重要作用。

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