Mitochondrial Localization of SARM1 in Acrylamide Intoxication Induces Mitophagy and Limits Neuropathy

• Published in: Molecular neurobiology 2022-12, Vol.59 (12), p.7337-7353
• Main Authors: Wang, Shuai, Song, Mingxue, Yong, Hui, Zhang, Cuiqin, Kang, Kang, Liu, Zhidan, Yang, Yiyu, Huang, Zhengcheng, Wang, Shu’e, Ge, Haotong, Zhao, Xiulan, Song, Fuyong
• Format: Article
• Language: English
• Subjects: Acrylamide; Adenyltransferase; Axotomy; Biomedical and Life Sciences; Biomedicine; Cell Biology; Death; Interleukin 1; Intoxication; Localization; Mitochondria; Mitophagy; Molecular modelling; Neurobiology; Neurodegeneration; Neurology; Neuropathy; Neurosciences; Nicotinamide; PTEN protein; PTEN-induced putative kinase; Rapamycin; Survival factor
• ISSN: 0893-7648; 1559-1182
• DOI: 10.1007/s12035-022-03050-8

Sterile α and toll/interleukin 1 receptor motif-containing protein 1 (SARM1) is the defining molecule and central executioner of programmed axon death, also known as Wallerian degeneration. SARM1 has a mitochondrial targeting sequence, and it can bind to and stabilize PTEN-induced putative kinase 1 (PINK1) for mitophagy induction, but the deletion of the mitochondrial localization sequence is found to disrupt the mitochondrial localization of SARM1 in neurons without altering its ability to promote axon degeneration after axotomy. The biological significance of SARM1 mitochondrial localization remains elusive. In this study, we observed that the pro-degeneration factor, SARM1, was upregulated in acrylamide (ACR) neuropathy, a slow, Wallerian-like, programmed axonal death process. The upregulated SARM1 accumulated on mitochondria, interfered with mitochondrial dynamics, and activated PINK1-mediated mitophagy. Importantly, rapamycin (RAPA) intervention eliminated mitochondrial accumulation of SARM1 and partly attenuated ACR neuropathy. Thus, mitochondrial localization of SARM1 may contribute to its clearance through the SARM1-PINK1 mitophagy pathway, which inhibits axonal degeneration through a negative feedback loop. The mitochondrial localization of SARM1 complements the coordinated activity of the pro-survival factor, nicotinamide mononucleotide adenyltransferase 2 (NMNAT2), and SARM1 and is part of the self-limiting molecular mechanisms underpinning programmed axon death in ACR neuropathy. Graphical abstract Mitophagy clearance of SARM1 is complementary to the coordinated activity of NMNAT2 and SARM1 in ACR neuropathy.