Pellegatta Marta, Taveggia Carla
Division of Neuroscience and INSPE at IRCCS San Raffaele Scientific Institute, Milan, Italy.
Front Cell Neurosci. 2019 Mar 20;13:93. doi: 10.3389/fncel.2019.00093. eCollection 2019.
After damage, axons in the peripheral nervous system (PNS) regenerate and regrow following a process termed Wallerian degeneration, but the regenerative process is often incomplete and usually the system does not reach full recovery. Key steps to the creation of a permissive environment for axonal regrowth are the trans-differentiation of Schwann cells and the remodeling of the extracellular matrix (ECM). In this review article, we will discuss how proteases and secretases promote effective regeneration and remyelination. We will detail how they control neuregulin-1 (NRG-1) activity at the post-translational level, as the concerted action of alpha, beta and gamma secretases cooperates to balance activating and inhibitory signals necessary for physiological myelination and remyelination. In addition, we will discuss the role of other proteases in nerve repair, among which A Disintegrin And Metalloproteinases (ADAMs) and gamma-secretases substrates. Moreover, we will present how matrix metalloproteinases (MMPs) and proteases of the blood coagulation cascade participate in forming newly synthetized myelin and in regulating axonal regeneration. Overall, we will highlight how a deeper comprehension of secretases and proteases mechanism of action in Wallerian degeneration might be useful to develop new therapies with the potential of readily and efficiently improve the regenerative process.
受损后,外周神经系统(PNS)中的轴突会按照沃勒变性过程进行再生和重新生长,但再生过程往往不完整,该系统通常无法完全恢复。为轴突再生创造有利环境的关键步骤是施万细胞的转分化和细胞外基质(ECM)的重塑。在这篇综述文章中,我们将讨论蛋白酶和分泌酶如何促进有效的再生和髓鞘再生。我们将详细阐述它们如何在翻译后水平控制神经调节蛋白-1(NRG-1)的活性,因为α、β和γ分泌酶的协同作用共同平衡生理髓鞘形成和髓鞘再生所需的激活信号和抑制信号。此外,我们将讨论其他蛋白酶在神经修复中的作用,其中包括解整合素和金属蛋白酶(ADAMs)以及γ分泌酶底物。此外,我们将介绍基质金属蛋白酶(MMPs)和凝血级联反应中的蛋白酶如何参与形成新合成的髓鞘以及调节轴突再生。总体而言,我们将强调深入理解分泌酶和蛋白酶在沃勒变性中的作用机制可能有助于开发新的疗法,这些疗法有可能轻松有效地改善再生过程。