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SARM1 can be a potential therapeutic target for spinal cord injury.SARM1 可能成为治疗脊髓损伤的一个潜在靶点。
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2
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Axon Self-Destruction: New Links among SARM1, MAPKs, and NAD+ Metabolism.轴突自我毁灭:SARM1、丝裂原活化蛋白激酶和烟酰胺腺嘌呤二核苷酸代谢之间的新联系
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本文引用的文献

1
Constitutively active SARM1 variants that induce neuropathy are enriched in ALS patients.在 ALS 患者中富集了诱导神经病变的组成性激活的 SARM1 变体。
Mol Neurodegener. 2022 Jan 6;17(1):1. doi: 10.1186/s13024-021-00511-x.
2
The SARM1 TIR NADase: Mechanistic Similarities to Bacterial Phage Defense and Toxin-Antitoxin Systems.SARM1 TIR NADase:与细菌噬菌体防御和毒素-抗毒素系统的机制相似性。
Front Immunol. 2021 Sep 23;12:752898. doi: 10.3389/fimmu.2021.752898. eCollection 2021.
3
Nicotinic acid mononucleotide is an allosteric SARM1 inhibitor promoting axonal protection.烟酰胺单核苷酸是一种别构 SARM1 抑制剂,可促进轴突保护。
Exp Neurol. 2021 Nov;345:113842. doi: 10.1016/j.expneurol.2021.113842. Epub 2021 Aug 14.
4
Acidic pH irreversibly activates the signaling enzyme SARM1.酸性 pH 值会不可逆地激活信号酶 SARM1。
FEBS J. 2021 Dec;288(23):6783-6794. doi: 10.1111/febs.16104. Epub 2021 Jul 13.
5
A phase transition enhances the catalytic activity of SARM1, an NAD glycohydrolase involved in neurodegeneration.相变增强了 SARM1 的催化活性,SARM1 是一种参与神经退行性变的 NAD 糖基水解酶。
Elife. 2021 Jun 29;10:e66694. doi: 10.7554/eLife.66694.
6
Genetic inactivation of SARM1 axon degeneration pathway improves outcome trajectory after experimental traumatic brain injury based on pathological, radiological, and functional measures.基于病理、影像学和功能测量,SARM1 轴突退化途径的遗传失活可改善实验性创伤性脑损伤后的转归轨迹。
Acta Neuropathol Commun. 2021 May 17;9(1):89. doi: 10.1186/s40478-021-01193-8.
7
Genetic diversity of axon degenerative mechanisms in models of Parkinson's disease.帕金森病模型中轴突退行性变机制的遗传多样性。
Neurobiol Dis. 2021 Jul;155:105368. doi: 10.1016/j.nbd.2021.105368. Epub 2021 Apr 20.
8
Sarm1-mediated neurodegeneration within the enteric nervous system protects against local inflammation of the colon.Sarm1 介导的肠神经退行性变可保护结肠免受局部炎症的侵害。
Protein Cell. 2021 Aug;12(8):621-638. doi: 10.1007/s13238-021-00835-w. Epub 2021 Apr 19.
9
An NAD+/NMN balancing act by SARM1 and NMNAT2 controls axonal degeneration.SARM1 和 NMNAT2 通过调节 NAD+/NMN 平衡来控制轴突变性。
Neuron. 2021 Apr 7;109(7):1067-1069. doi: 10.1016/j.neuron.2021.03.021.
10
SARM1 promotes neuroinflammation and inhibits neural regeneration after spinal cord injury through NF-κB signaling.甾体类雄激素受体调节剂1(SARM1)通过核因子κB(NF-κB)信号通路促进脊髓损伤后的神经炎症并抑制神经再生。
Theranostics. 2021 Feb 20;11(9):4187-4206. doi: 10.7150/thno.49054. eCollection 2021.

SARM1 可能成为治疗脊髓损伤的一个潜在靶点。

SARM1 can be a potential therapeutic target for spinal cord injury.

机构信息

Department of Histology and Embryology, Medical College, Shaoxing University, Shaoxing, China.

Institute of Neuroscience, Zhejiang University School of Medicine, Hangzhou, China.

出版信息

Cell Mol Life Sci. 2022 Feb 28;79(3):161. doi: 10.1007/s00018-022-04195-4.

DOI:10.1007/s00018-022-04195-4
PMID:35224705
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11072485/
Abstract

Injury to the spinal cord is devastating. Studies have implicated Wallerian degeneration as the main cause of axonal destruction in the wake of spinal cord injury. Therefore, the suppression of Wallerian degeneration could be beneficial for spinal cord injury treatment. Sterile alpha and armadillo motif-containing protein 1 (SARM1) is a key modulator of Wallerian degeneration, and its impediment can improve spinal cord injury to a significant degree. In this report, we analyze the various signaling domains of SARM1, the recent findings on Wallerian degeneration and its relation to axonal insults, as well as its connection to SARM1, the mitogen-activated protein kinase (MAPK) signaling, and the survival factor, nicotinamide mononucleotide adenylyltransferase 2 (NMNAT2). We then elaborate on the possible role of SARM1 in spinal cord injury and explicate how its obstruction could potentially alleviate the injury.

摘要

脊髓损伤是毁灭性的。研究表明,Wallerian 变性是脊髓损伤后轴突破坏的主要原因。因此,抑制 Wallerian 变性可能有益于脊髓损伤的治疗。无菌α和装甲蛋白 1(SARM1)是 Wallerian 变性的关键调节剂,其抑制作用可显著改善脊髓损伤。在本报告中,我们分析了 SARM1 的各种信号结构域、Wallerian 变性及其与轴突损伤的关系的最新发现,以及它与丝裂原活化蛋白激酶(MAPK)信号和生存因子烟酰胺单核苷酸腺苷酰转移酶 2(NMNAT2)的关系。然后,我们详细阐述了 SARM1 在脊髓损伤中的可能作用,并解释了其阻断如何可能减轻损伤。