Hematopoietic loss of Y chromosome leads to cardiac fibrosis and heart failure mortality.
clonal hematopoiesis
Journal
Science (New York, N.Y.)
ISSN: 1095-9203
Titre abrégé: Science
Pays: United States
ID NLM: 0404511
Informations de publication
Date de publication:
15 07 2022
15 07 2022
Historique:
entrez:
20
7
2022
pubmed:
21
7
2022
medline:
23
7
2022
Statut:
ppublish
Résumé
Hematopoietic mosaic loss of Y chromosome (mLOY) is associated with increased risk of mortality and age-related diseases in men, but the causal and mechanistic relationships have yet to be established. Here, we show that male mice reconstituted with bone marrow cells lacking the Y chromosome display increased mortality and age-related profibrotic pathologies including reduced cardiac function. Cardiac macrophages lacking the Y chromosome exhibited polarization toward a more fibrotic phenotype, and treatment with a transforming growth factor β1-neutralizing antibody ameliorated cardiac dysfunction in mLOY mice. A prospective study revealed that mLOY in blood is associated with an increased risk for cardiovascular disease and heart failure-associated mortality. Together, these results indicate that hematopoietic mLOY causally contributes to fibrosis, cardiac dysfunction, and mortality in men.
Identifiants
pubmed: 35857592
doi: 10.1126/science.abn3100
pmc: PMC9437978
mid: NIHMS1830716
doi:
Substances chimiques
Antibodies, Neutralizing
0
Transforming Growth Factor beta
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
292-297Subventions
Organisme : NIGMS NIH HHS
ID : T32 GM007267
Pays : United States
Organisme : Medical Research Council
ID : MC_PC_17228
Pays : United Kingdom
Organisme : NHLBI NIH HHS
ID : R01 HL142650
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL141256
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL146056
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL139819
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL152174
Pays : United States
Organisme : Medical Research Council
ID : MC_QA137853
Pays : United Kingdom
Organisme : NIA NIH HHS
ID : R01 AG073249
Pays : United States
Organisme : NIA NIH HHS
ID : R21 AG072095
Pays : United States
Commentaires et corrections
Type : CommentIn
Type : CommentIn
Type : CommentIn
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