
Collapsin Response Mediator Proteins: Novel Targets for Alzheimer’s Disease
Author(s) -
Tam Quach,
Aubin Moutal,
Rajesh Khanna,
Nicholas P. Deems,
AnneMarie Duchemin,
Ruth M. Barrientos
Publication year - 2020
Publication title -
journal of alzheimer's disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.677
H-Index - 139
eISSN - 1875-8908
pISSN - 1387-2877
DOI - 10.3233/jad-200721
Subject(s) - mediator , neuroscience , dendritic spine , neurite , biology , disease , hippocampus , axon guidance , axon , psychology , microbiology and biotechnology , medicine , pathology , hippocampal formation , biochemistry , in vitro
Numerous experimental and postmortem studies have increasingly reported dystrophic axons and dendrites, and alterations of dendritic spine morphology and density in the hippocampus as prominent changes in the early stages of Alzheimer's disease (AD). Furthermore, these alterations tend to correlate well with the progressive cognitive decline observed in AD. For these reasons, and because these neurite structures have a capacity to re-grow, re-establish lost connections, and are critical for learning and memory, there is compelling evidence to suggest that therapeutic interventions aimed at preventing their degradation or promoting their regrowth may hold tremendous promise in preventing the progression of AD. In this regard, collapsin response mediator proteins (CRMPs), a family of phosphoproteins playing a major role in axon guidance and dendritic growth, are especially interesting. The roles these proteins play in neurons and immune cells are reviewed here.