Associations of cortical SPP1 and ITGAX with cognition and common neuropathologies in older adults

Author:

Lopes Katia de Paiva12,Yu Lei12,Shen Xianli34,Qiu Yiguo345,Tasaki Shinya12,Iatrou Artemis126,Beeri Michal Schnaider789,Seyfried Nicholas T.10,Menon Vilas11,Wang Yanling12,Schneider Julie A.1212,Cantor Harvey34,Bennett David A.12

Affiliation:

1. Rush Alzheimer's Disease Center Rush University Medical Center Chicago Illinois USA

2. Department of Neurological Sciences Rush University Medical Center Chicago Illinois USA

3. Department of Cancer Immunology and Virology Dana‐Farber Cancer Institute Boston Massachusetts USA

4. Department of Immunology Harvard Medical School Boston Massachusetts USA

5. Chongqing International Institute for Immunology Chongqing China

6. Department of Psychiatry, McLean Hospital Harvard Medical School Belmont Massachusetts USA

7. Joseph Sagol Neuroscience Center, Sheba Medical Center Ramat Gan Israel

8. Department of Psychiatry Icahn School of Medicine at Mount Sinai New York New York USA

9. The Herbert and Jackeline Krieger Klein Alzheimer's Research Center Rutgers Biomedical and Health Sciences, Rutgers University New Jersey USA

10. Goizueta Alzheimer's Disease Research Center, Department of Neurology and Department of Biochemistry Emory University School of Medicine Atlanta Georgia USA

11. Center for Translational and Computational Neuroimmunology Department of Neurology & Taub Institute for Research on Alzheimer's disease and the Aging Brain Columbia University Irving Medical Center New York New York USA

12. Department of Pathology Rush University Medical Center Chicago Illinois USA

Abstract

AbstractINTRODUCTIONThe secreted phosphoprotein 1 (SPP1) gene expressed by CD11c+ cells is known to be associated with microglia activation and neuroinflammatory diseases. As most studies rely on mouse models, we investigated these genes and proteins in the cortical brain tissue of older adults and their role in Alzheimer's disease (AD) and related disorders.METHODSWe leveraged protein measurements, single‐nuclei, and RNASeq data from the Religious Orders Study and Rush Memory and Aging Project (ROSMAP) of over 1200 samples for association analysis.RESULTSExpression of SPP1 and its encoded protein osteopontin were associated with faster cognitive decline and greater odds of common neuropathologies. At single‐cell resolution,  integrin subunit alpha X (ITGAX) was highly expressed in microglia, where specific subpopulations were associated with AD and cerebral amyloid angiopathy.DISCUSSIONThe study provides evidence of SPP1 and ITGAX association with cognitive decline and common neuropathologies identifying a microglial subset associated with disease.

Funder

National Institute on Aging

Publisher

Wiley

Subject

Psychiatry and Mental health,Cellular and Molecular Neuroscience,Geriatrics and Gerontology,Neurology (clinical),Developmental Neuroscience,Health Policy,Epidemiology

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