Title

Rac1b increases with progressive tau pathology within cholinergic nucleus basalis neurons in alzheimer's disease

Document Type

Article

Abstract

Cholinergic basal forebrain (CBF) nucleus basalis (NB) neurons display neurofibrillary tangles (NFTs) during Alzheimer's disease (AD) progression, yet the mechanisms underlying this selective vulnerability are currently unclear. Rac1, a member of the Rho family of GTPases, may interact with the proapoptotic pan-neurotrophin receptor p75 NTR to induce neuronal cytoskeletal abnormalities in AD NB neurons. Herein, we examined the expression of Rac1b, a constitutively active splice variant of Rac1, in NB cholinergic neurons during AD progression. CBF tissues harvested from people who died with a clinical diagnosis of no cognitive impairment (NCI), mild cognitive impairment, or AD were immunolabeled for both p75 NTR and Rac1b. Rac1b appeared as cytoplasmic diffuse granules, loosely aggregated filaments, or compact spheres in p75 NTR-positive NB neurons. Although Rac1b colocalized with tau cytoskeletal markers, the percentage of p75 NTR-immunoreactive neurons expressing Rac1b was significantly increased only in AD compared with both mild cognitive impairment and NCI. Furthermore, single-cell gene expression profiling with custom-designed microarrays showed down-regulation of caveolin 2, GNB4, and lipase A in AD Rac1b-positive/p75 NTR-labeled NB neurons compared with Rac1b-negative/p75 NTR-positive perikarya in NCI. These proteins are involved in Rac1 pathway/cell cycle progression and lipid metabolism. These data suggest that Rac1b expression acts as a modulator or transducer of various signaling pathways that lead to NFT formation and membrane dysfunction in a subgroup of CBF NB neurons in AD. © 2012 American Society for Investigative Pathology.

Publication Date

2-1-2012

Publication Title

American Journal of Pathology

ISSN

00029440

E-ISSN

15252191

Volume

180

Issue

2

First Page

526

Last Page

540

PubMed ID

22142809

Digital Object Identifier (DOI)

10.1016/j.ajpath.2011.10.027

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