A new gene set identifies senescent cells and predicts senescence-associated pathways across tissues
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Published:2022-08-16
Issue:1
Volume:13
Page:
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ISSN:2041-1723
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Container-title:Nature Communications
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language:en
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Short-container-title:Nat Commun
Author:
Saul DominikORCID, Kosinsky Robyn LauraORCID, Atkinson Elizabeth J., Doolittle Madison L., Zhang XuORCID, LeBrasseur Nathan K.ORCID, Pignolo Robert J., Robbins Paul D.ORCID, Niedernhofer Laura J.ORCID, Ikeno Yuji, Jurk DianaORCID, Passos João F.ORCID, Hickson LaTonya J., Xue Ailing, Monroe David G.ORCID, Tchkonia TamaraORCID, Kirkland James L.ORCID, Farr Joshua N.ORCID, Khosla SundeepORCID
Abstract
AbstractAlthough cellular senescence drives multiple age-related co-morbidities through the senescence-associated secretory phenotype, in vivo senescent cell identification remains challenging. Here, we generate a gene set (SenMayo) and validate its enrichment in bone biopsies from two aged human cohorts. We further demonstrate reductions in SenMayo in bone following genetic clearance of senescent cells in mice and in adipose tissue from humans following pharmacological senescent cell clearance. We next use SenMayo to identify senescent hematopoietic or mesenchymal cells at the single cell level from human and murine bone marrow/bone scRNA-seq data. Thus, SenMayo identifies senescent cells across tissues and species with high fidelity. Using this senescence panel, we are able to characterize senescent cells at the single cell level and identify key intercellular signaling pathways. SenMayo also represents a potentially clinically applicable panel for monitoring senescent cell burden with aging and other conditions as well as in studies of senolytic drugs.
Funder
Dr. Mildred Scheel Stiftung für Krebsforschung Foundation for the National Institutes of Health
Publisher
Springer Science and Business Media LLC
Subject
General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry,Multidisciplinary
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