Department of Physiology, Mitochondria Hub Regulation Center, College of Medicine, Dong-A University, Busan 602-714, South Korea.
J Neurosci. 2011 Feb 9;31(6):2009-15. doi: 10.1523/JNEUROSCI.4537-10.2011.
The mechanisms that trigger Wallerian degeneration (WD) of peripheral nerves after injury are not well understood. During the early period of WD, fragmentation of myelin into ovoid structures occurs near the Schmidt-Lantermann incisures (SLI), a noncompact region of the myelin sheath containing autotypical adherens junction. In this study, we found that new filamentous actin polymerization occurs in the SLI of mouse sciatic nerves after injury and that its inhibition prevented not only the degradation of E-cadherin in the SLI but also myelin ovoid formation. However, the inhibition of actin polymerization could not block Schwann cell dedifferentiation. The activation of Rac GTPase was observed in the distal stump of the injured nerves, and a specific Rac inhibitor, a dominant-negative Rac, and Rac1-RNA interference blocked myelin ovoid formation. Together, these findings suggest that dynamic changes in actin in the SLI are essential for initiation of demyelination after peripheral nerve injury.
神经损伤后引发 Wallerian 变性(WD)的机制尚不清楚。在 WD 的早期阶段,髓鞘在施密特-兰登曼切迹(SLI)附近碎裂成卵圆形结构,SLI 是髓鞘的非致密区,包含典型的黏着连接。在这项研究中,我们发现小鼠坐骨神经损伤后 SLI 中出现新的丝状肌动蛋白聚合,其抑制不仅防止了 SLI 中 E-钙黏蛋白的降解,也阻止了髓鞘卵圆形的形成。然而,肌动蛋白聚合的抑制并不能阻止施万细胞去分化。在损伤神经的远端残端观察到 Rac GTPase 的激活,而一种特异性 Rac 抑制剂、显性失活 Rac 和 Rac1-RNA 干扰则阻断了髓鞘卵圆形的形成。总之,这些发现表明 SLI 中肌动蛋白的动态变化对于周围神经损伤后脱髓鞘的起始是必不可少的。