| Literature DB >> 19841538 |
Charles T Esmon1, Jonathan D Glass.
Abstract
Mutations in the enzyme superoxide dismutase 1 (SOD1) have been linked to the neurodegenerative disease amyotrophic lateral sclerosis (ALS). In this issue of the JCI, Zhong et al. report that the endogenous anticoagulant activated protein C (APC) is able to cross the blood-spinal cord barrier in mice and signal to both neuronal and non-neuronal cells (see the related article beginning on page 3437). This signaling resulted in the suppression of mutant SOD1 synthesis and retarded disease progression in a murine model of ALS. Here we discuss the potential importance of these data and possible relevance to human neurodegenerative diseases.Entities:
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Year: 2009 PMID: 19841538 PMCID: PMC2769189 DOI: 10.1172/JCI40682
Source DB: PubMed Journal: J Clin Invest ISSN: 0021-9738 Impact factor: 14.808