Posterior cingulate cortex reveals an expression profile of resilience in cognitively intact elders

Authors

Christy M. Kelley, Department of Translational Neuroscience, Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, AZ 85013, USA.
Stephen D. Ginsberg, Center for Dementia Research, Nathan Kline Institute, Orangeburg, NY 10962, USA.
Winnie S. Liang, Translational Genomics Research Institute, Phoenix, AZ 85004, USA.
Scott E. Counts, Department of Translational Neuroscience, Michigan State University College of Human Medicine, Grand Rapids, MI 49503, USA.
Elliott J. Mufson, Department of Translational Neuroscience, Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, AZ 85013, USA.

Document Type

Article

Abstract

The posterior cingulate cortex, a key hub of the default mode network, underlies autobiographical memory retrieval and displays hypometabolic changes early in Alzheimer disease. To obtain an unbiased understanding of the molecular pathobiology of the aged posterior cingulate cortex, we performed RNA sequencing (RNA-seq) on tissue obtained from 26 participants of the Rush Religious Orders Study (11 males/15 females; aged 76-96 years) with a pre-mortem clinical diagnosis of no cognitive impairment and post-mortem neurofibrillary tangle Braak Stages I/II, III, and IV. Transcriptomic data were gathered using next-generation sequencing of RNA extracted from posterior cingulate cortex generating an average of 60 million paired reads per subject. Normalized expression of RNA-seq data was calculated using a global gene annotation and a microRNA profile. Differential expression (DESeq2, edgeR) using Braak staging as the comparison structure isolated genes for dimensional scaling, associative network building and functional clustering. Curated genes were correlated with the Mini-Mental State Examination and semantic, working and episodic memory, visuospatial ability, and a composite Global Cognitive Score. Regulatory mechanisms were determined by co-expression networks with microRNAs and an overlap of transcription factor binding sites. Analysis revealed 750 genes and 12 microRNAs significantly differentially expressed between Braak Stages I/II and III/IV and an associated six groups of transcription factor binding sites. Inputting significantly different gene/network data into a functional annotation clustering model revealed elevated presynaptic, postsynaptic and ATP-related expression in Braak Stages III and IV compared with Stages I/II, suggesting these pathways are integral for cognitive resilience seen in unimpaired elderly subjects. Principal component analysis and Kruskal-Wallis testing did not associate Braak stage with cognitive function. However, Spearman correlations between genes and cognitive test scores followed by network analysis revealed upregulation of classes of synaptic genes positively associated with performance on the visuospatial perceptual orientation domain. Upregulation of key synaptic genes suggests a role for these transcripts and associated synaptic pathways in cognitive resilience seen in elders despite Alzheimer disease pathology and dementia.

Keywords

RNA-Seq, aging, cognition, human, posterior cingulate cortex

Publication Date

1-1-2022

Publication Title

Brain communications

E-ISSN

2632-1297

Volume

4

Issue

4

First Page

fcac162

PubMed ID

35813880

Digital Object Identifier (DOI)

10.1093/braincomms/fcac162

Recommended Citation

Kelley, Christy M.; Ginsberg, Stephen D.; Liang, Winnie S.; Counts, Scott E.; and Mufson, Elliott J., "Posterior cingulate cortex reveals an expression profile of resilience in cognitively intact elders" (2022). Translational Neuroscience. 2278.
https://scholar.barrowneuro.org/neurobiology/2278