Establishing the relationship between brain cellular senescence and brain structure.

TitleEstablishing the relationship between brain cellular senescence and brain structure.
Publication TypeJournal Article
Year of Publication2026
AuthorsLund AN, Kopell BH, Golestani N, Vornholt E, Thompson RC, Liharska LE, Luo Y, Cheng E, Park YJeong, Fennessy B, Wilkins L, Kaji DA, Silk H, Ziafat K, Hashemi A, Moya E, Feng C, Linares LM, Grice ABuxbaum, Xie S, Rieder M-K, Scarpa J, Kota P, Cohen V, Sullivan B, Shah P, Ma W, Johnson JS, Miller GM, Searfoss R, Chand NMahaveer, Wang P, Nadkarni GN, Narain NR, Nestler EJ, Kiebish MA, Schadt EE, Charney AW, Beckmann ND
JournalCell
Volume189
Issue2
Pagination511-527.e17
Date Published2026 Jan 22
ISSN1097-4172
KeywordsAdolescent, Adult, Aged, Aging, Atrophy, Brain, Cellular Senescence, Child, Preschool, Female, Humans, Male, Microglia, Middle Aged, Neuroimaging, Neurons, Prefrontal Cortex, Young Adult
Abstract

Cellular senescence and brain atrophy are both associated with brain aging, suggesting these processes may share underlying biological mechanisms. This study investigated these mechanisms by integrating structural neuroimaging with gene and protein expression data from prefrontal cortex tissue collected from individuals who underwent neurosurgery. Cell-type-specific gene expression signatures associated with neuroimaging features and cellular senescence were identified and replicated in several independent datasets. Significant correlations between these signatures were observed in excitatory neurons and microglia, especially for volume-related features. These associations were also observed for excitatory neurons in an independent brain gene expression dataset from individuals below 5 years of age, implying a role for senescence during brain development. Together, this study provides a deep characterization of molecular signatures linking brain structure and cellular senescence across different life stages and suggests mechanisms supporting brain development may also contribute to volume reduction observed during aging.

DOI10.1016/j.cell.2025.10.014
Alternate JournalCell
PubMed ID41576919