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作 者:Yanni Duan Fengguang Yang Yibao Zhang Mingtao Zhang Yujun Shi Yun Lang Hongli Sun Xin Wang Hongyun Jin Xuewen Kang
机构地区:[1]Department of Orthopedics,The Second Hospital of Lanzhou University,Lanzhou,Gansu Province,China [2]The Second Clinical Medical School,Lanzhou University,Lanzhou,Gansu Province,China [3]Orthopaedics Key Laboratory of Gansu Province,The Second Hospital of Lanzhou University,Lanzhou,Gansu Province,China
出 处:《Neural Regeneration Research》2026年第2期598-611,共14页中国神经再生研究(英文版)
基 金:supported by Cuiying Scientific and Technological Innovation Program of Second Hospital of Lanzhou University,Nos.CY2023-QN-B18(to YD),2020QN-16(to YZ);the Natural Science Foundation of Gansu Province,No.22JR11RA082(to YZ);Key R&D Plan of Gansu Provincial Department of Science and Technology-Social Development Projects,No.23YFFA0043(to XK).
摘 要:Spinal cord ischemia-reperfusion injury,a severe form of spinal cord damage,can lead to sensory and motor dysfunction.This injury often occurs after traumatic events,spinal cord surgeries,or thoracoabdominal aortic surgeries.The unpredictable nature of this condition,combined with limited treatment options,poses a significant burden on patients,their families,and society.Spinal cord ischemia-reperfusion injury leads to reduced neuronal regenerative capacity and complex pathological processes.In contrast,mitophagy is crucial for degrading damaged mitochondria,thereby supporting neuronal metabolism and energy supply.However,while moderate mitophagy can be beneficial in the context of spinal cord ischemia-reperfusion injury,excessive mitophagy may be detrimental.Therefore,this review aims to investigate the potential mechanisms and regulators of mitophagy involved in the pathological processes of spinal cord ischemia-reperfusion injury.The goal is to provide a comprehensive understanding of recent advancements in mitophagy related to spinal cord ischemia-reperfusion injury and clarify its potential clinical applications.
关 键 词:BNIP3 BNIP3L/NIX FUNDC1 mechanism MITOCHONDRIA MITOPHAGY modulators PARKIN PINK1 spinal cord ischemia-reperfusion injury
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