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脊髓损伤发病机制和治疗中的程序性细胞死亡。

Programmed cell death in spinal cord injury pathogenesis and therapy.

机构信息

Department of Orthopaedics, Tianjin Medical University General Hospital, Tianjin, China.

School of Medicine, Nankai University, Tianjin, China.

出版信息

Cell Prolif. 2021 Mar;54(3):e12992. doi: 10.1111/cpr.12992. Epub 2021 Jan 27.


DOI:10.1111/cpr.12992
PMID:33506613
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7941236/
Abstract

Spinal cord injury (SCI) always leads to functional deterioration due to a series of processes including cell death. In recent years, programmed cell death (PCD) is considered to be a critical process after SCI, and various forms of PCD were discovered in recent years, including apoptosis, necroptosis, autophagy, ferroptosis, pyroptosis and paraptosis. Unlike necrosis, PCD is known as an active cell death mediated by a cascade of gene expression events, and it is crucial for elimination unnecessary and damaged cells, as well as a defence mechanism. Therefore, it would be meaningful to characterize the roles of PCD to not only enhance our understanding of the pathophysiological processes, but also improve functional recovery after SCI. This review will summarize and explore the most recent advances on how apoptosis, necroptosis, autophagy, ferroptosis, pyroptosis and paraptosis are involved in SCI. This review can help us to understand the various functions of PCD in the pathological processes of SCI, and contribute to our novel understanding of SCI of unknown aetiology in the near future.

摘要

脊髓损伤 (SCI) 总是会导致功能恶化,这是一系列过程的结果,包括细胞死亡。近年来,程序性细胞死亡 (PCD) 被认为是 SCI 后的一个关键过程,近年来发现了多种形式的 PCD,包括细胞凋亡、坏死性凋亡、自噬、铁死亡、细胞焦亡和副凋亡。与坏死不同,PCD 是一种由基因表达事件级联介导的主动细胞死亡,它对于消除不必要和受损的细胞以及作为一种防御机制至关重要。因此,描述 PCD 的作用具有重要意义,不仅可以加深我们对病理生理过程的理解,还可以改善 SCI 后的功能恢复。本综述将总结和探讨细胞凋亡、坏死性凋亡、自噬、铁死亡、细胞焦亡和副凋亡如何参与 SCI 的最新进展。这篇综述可以帮助我们理解 PCD 在 SCI 病理过程中的各种功能,并有助于我们在不久的将来对未知病因的 SCI 有新的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ede/7941236/232f08fa0e26/CPR-54-e12992-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ede/7941236/232f08fa0e26/CPR-54-e12992-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ede/7941236/232f08fa0e26/CPR-54-e12992-g001.jpg

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Programmed cell death in spinal cord injury pathogenesis and therapy.

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引用本文的文献

[1]
Microglial pyroptosis as a therapeutic target after traumatic spinal cord injury: current progress and future directions.

Front Immunol. 2025-8-22

[2]
Exosomes-Based Nanotherapeutic Strategies: An Important Approach for Spinal Cord Injury Repair.

Int J Nanomedicine. 2025-8-27

[3]
Genome-Wide Identification of Microglia-Related RNA-Binding Proteins and Regulated Alternative Splicing in Spinal Cord Injury.

ACS Omega. 2025-8-12

[4]
The Temporal and Spatial Distribution Patterns of Necrotic and Apoptotic Cells in and Around the Spinal Cord Injury Site.

Diagnostics (Basel). 2025-8-18

[5]
A Review of Pathophysiology, Molecular Mechanisms, and Omics Approaches of Spinal Cord Injury.

Int J Mol Sci. 2025-8-15

[6]
Oxidative stress and programmed cell death in diabetic wounds: A comprehensive review.

Sci Prog. 2025

[7]
Comprehensive landscape of cell death mechanisms: from molecular cross-talk to therapeutic innovation in oncology.

Front Cell Dev Biol. 2025-7-16

[8]
Quercetin targets the Ccl4-Ccr5 axis to relieve neuropathic pain after spinal cord injury.

APL Bioeng. 2025-7-24

[9]
Bacterial programmed cell death and toxin-antitoxin system in bacteria.

Arch Microbiol. 2025-7-21

[10]
Targeting ferroptosis in spinal cord injury through stem cell therapy: mechanisms and therapeutic prospects.

Front Neurosci. 2025-6-25

本文引用的文献

[1]
Therapeutic effect of metformin on inflammation and apoptosis after spinal cord injury in rats through the Wnt/β-catenin signaling pathway.

Neurosci Lett. 2020-11-20

[2]
Deficiency of the microglial Hv1 proton channel attenuates neuronal pyroptosis and inhibits inflammatory reaction after spinal cord injury.

J Neuroinflammation. 2020-9-5

[3]
Role of ABT888, a Novel Poly(ADP-Ribose) Polymerase (PARP) Inhibitor in Countering Autophagy and Apoptotic Processes Associated to Spinal Cord Injury.

Mol Neurobiol. 2020-11

[4]
Proanthocyanidin promotes functional recovery of spinal cord injury via inhibiting ferroptosis.

J Chem Neuroanat. 2020-9

[5]
Neuroprotective effect of deferoxamine on erastininduced ferroptosis in primary cortical neurons.

Neural Regen Res. 2020-8

[6]
Targeting CARD6 attenuates spinal cord injury (SCI) in mice through inhibiting apoptosis, inflammation and oxidative stress associated ROS production.

Aging (Albany NY). 2019-12-16

[7]
Progranulin deficiency exacerbates spinal cord injury by promoting neuroinflammation and cell apoptosis in mice.

J Neuroinflammation. 2019-11-27

[8]
Critical Role of p38 in Spinal Cord Injury by Regulating Inflammation and Apoptosis in a Rat Model.

Spine (Phila Pa 1976). 2020-4-1

[9]
Autophagy-dependent cell death.

Cell Death Differ. 2018-12-19

[10]
Role of pyroptosis in cardiovascular disease.

Cell Prolif. 2018-12-7

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