Role of necroptosis in traumatic brain and spinal cord injuries

被引:39
作者
Hu, Xinli
Xu, Yu
Zhang, Haojie
Li, Yao
Wang, Xiangyang [1 ]
Xu, Cong [1 ]
Ni, Wenfei [1 ]
Zhou, Kailiang [1 ]
机构
[1] Wenzhou Med Univ, Affiliated Hosp & Yuying Childrens Hosp 2, Dept Orthopaed, 109 West Xueyuan Rd, Wenzhou 325027, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Necroptosis; Cell death; Spinal cord injury; Traumatic brain injury; CNS trauma; ENDOPLASMIC-RETICULUM STRESS; MIXED LINEAGE KINASE; DOMAIN-LIKE PROTEIN; PROGRAMMED CELL-DEATH; MOLECULAR-MECHANISMS; RIP1; KINASE; MEDIATED APOPTOSIS; IN-VITRO; NECROSIS; PHOSPHORYLATION;
D O I
10.1016/j.jare.2021.12.002
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Traumatic brain injury (TBI) and spinal cord injury (SCI) are capable of causing severe sen-sory, motor and autonomic nervous system dysfunctions. However, effective treatments for TBI and SCI are still unavailable, mainly because the death of nerve cells is uncontrollable. Necroptosis is a type of programmed cell death and a critical mechanism in the process of neuronal cell death. However, the role of necroptosis has not been comprehensively defined in TBI and SCI.Aim of review: This review aimed to summarize the role of necroptosis in central nervous system (CNS) trauma and its therapeutic implications and present important suggestions for researchers conducting in-depth research.Key scientific concepts of review: Necroptosis is orchestrated by a complex comprising the receptor -interacting protein kinase (RIPK)1, RIPK3 and mixed lineage kinase domain-like protein (MLKL) proteins. Mechanistically, RIPK1 and RIPK3 form a necrosome with MLKL. After MLKL dissociates from the necro-some, it translocates to the plasma membrane to induce pore formation in the membrane and then induces necroptosis. In this review, the necroptosis signalling pathway and the execution of necroptosis are briefly discussed. In addition, we focus on the existing information on the mechanism by which necroptosis participates in CNS trauma, particularly in the temporal pattern of RIPKs and in different cell types. Furthermore, we describe the association of miRNAs and necroptosis and the relationship between different types of CNS trauma cell death. Finally, this study highlights agents likely capable of curtailing such a type of cell death according to results optimization and CNS trauma and presents important sug-gestions for researchers conducting in-depth research.(c) 2022 The Authors. Published by Elsevier B.V. on behalf of Cairo University. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:125 / 134
页数:10
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