| Literature DB >> 32086246 |
Sienna Drake1, Alyson Fournier2.
Abstract
The protein Nogo-A has been widely studied for its role in inhibiting axonal regeneration following injury to the central nervous system, but the mechanism by which the membrane-bound Nogo-A is presented intercellularly is not fully understood. New research suggests that a highly inhibitory fragment of Nogo-A is generated by the amyloid precursor protein protease BACE1 and presented on the membranes of exosomes following spinal cord injury. This finding represents a new mode through which Nogo-A may exert its effects in the central nervous system.Entities:
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Year: 2020 PMID: 32086246 PMCID: PMC7039564 DOI: 10.1074/jbc.H120.012745
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157