Aydın Mehmet Şerif, Bay Sadık, Yiğit Esra Nur, Özgül Cemil, Oğuz Elif Kaval, Konuk Elçin Yenidünya, Ayşit Neşe, Cengiz Nureddin, Erdoğan Ender, Him Aydın, Koçak Mehmet, Eroglu Emrah, Öztürk Gürkan
Regenerative and Restorative Medicine Research Center (REMER), Research Institute for Health Sciences and Technologies (SABITA), Istanbul Medipol University, Istanbul 34810, Türkiye.
Department of Science Education, Faculty of Education, Yüzüncü Yıl University, Van 65080, Türkiye.
iScience. 2023 Aug 25;26(10):107715. doi: 10.1016/j.isci.2023.107715. eCollection 2023 Oct 20.
Trauma, vascular events, or neurodegenerative processes can lead to axonal injury and eventual transection (axotomy). Neurons can survive axotomy, yet the underlying mechanisms are not fully understood. Excessive water entry into injured neurons poses a particular risk due to swelling and subsequent death. Using and neurotrauma model systems based on laser transection and surgical nerve cut, we demonstrated that axotomy triggers actomyosin contraction coupled with calpain activity. As a consequence, neurons shrink acutely to force water out through aquaporin channels preventing swelling and bursting. Inhibiting shrinkage increased the probability of neuronal cell death by about 3-fold. These studies reveal a previously unrecognized cytoprotective response mechanism to neurotrauma and offer a fresh perspective on pathophysiological processes in the nervous system.
创伤、血管事件或神经退行性过程可导致轴突损伤及最终横断(轴突切断术)。神经元能够在轴突切断术后存活,但其潜在机制尚未完全明确。由于肿胀及随后的死亡,过多水分进入受损神经元会带来特别的风险。利用基于激光横断和外科神经切断的神经创伤模型系统,我们证明轴突切断术会引发肌动球蛋白收缩并伴有钙蛋白酶活性。结果,神经元会急剧收缩,迫使水分通过水通道蛋白通道排出,从而防止肿胀和破裂。抑制收缩会使神经元细胞死亡的概率增加约3倍。这些研究揭示了一种此前未被认识到的针对神经创伤的细胞保护反应机制,并为神经系统的病理生理过程提供了新的视角。