Affiliation:
1. Genetics and Genome Biology Program, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada
2. Department of Molecular Genetics, University of Toronto, Toronto, ON M5S 1A1, Canada
Abstract
Microglial and astrocytic reactivity is a prominent feature of amyotrophic lateral sclerosis (ALS). Microglia and astrocytes have been increasingly appreciated to play pivotal roles in disease pathogenesis. These cells can adopt distinct states characterized by a specific molecular profile or function depending on the different contexts of development, health, aging, and disease. Accumulating evidence from ALS rodent and cell models has demonstrated neuroprotective and neurotoxic functions from microglia and astrocytes. In this review, we focused on the recent advancements of knowledge in microglial and astrocytic states and nomenclature, the landmark discoveries demonstrating a clear contribution of microglia and astrocytes to ALS pathogenesis, and novel therapeutic candidates leveraging these cells that are currently undergoing clinical trials.
Funder
ALS Society of Canada, Brain Canada, ALS Association, and Canadian Institutes of Health Research
David Dime Family Catalyst Initiative in Molecular Genetics at the University of Toronto
Canada Graduate Scholarship-Master’s Program
University of Toronto-Fellowship
Restracomp from The Hospital of Sick Children
Subject
General Agricultural and Biological Sciences,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology
Cited by
10 articles.
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