ASK1 activation in glial cells in post‐mortem multiple sclerosis tissue

Author:

Seki Erika1ORCID,Guo Xiaoli2ORCID,Namekata Kazuhiko2,Komori Takashi3,Hayashi Hiroyuki4,Arai Nobutaka3,Harada Takayuki2

Affiliation:

1. Laboratory of Molecular Pathology and Histology Tokyo Metropolitan Institute of Medical Science Tokyo Japan

2. Visual Research Project Tokyo Metropolitan Institute of Medical Science Tokyo Japan

3. Department of Laboratory Medicine and Pathology (Neuropathology) Tokyo Metropolitan Neurological Hospital Tokyo Japan

4. Department of Pathology Yokohama Municipal Citizen's Hospital Kanagawa Japan

Abstract

Multiple sclerosis (MS), the leading cause of disability in young adults, is an inflammatory disease of the central nervous system characterized by localized areas of demyelination. Apoptosis signal‐regulating kinase 1 (ASK1) is a mitogen‐activated protein kinase kinase kinase that has been shown to be implicated in the pathogenesis of experimental autoimmune encephalomyelitis (EAE), a mouse model of MS. Interestingly, ASK1 signaling regulates glial cell interactions and drives neuroinflammation in EAE mice. To further investigate its clinical significance, in the present study, we examined the activation of ASK1 in the post‐mortem brain of MS patients. ASK1 activation was found in active lesions of the corpus callosum in both microglia/macrophages and astrocytes. Moreover, ASK1 activation in astrocytes was higher than that in microglia/macrophages, which was in line with our findings in EAE mice. Our results suggest an important role of ASK1 in glial cells, indicating that ASK1 might be a good therapeutic target for MS.

Publisher

Wiley

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Asking one mechanism in glial cells during neuroinflammation;Neural Regeneration Research;2024-06-03

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