| Literature DB >> 35857592 |
Soichi Sano1,2, Keita Horitani1, Hayato Ogawa1, Jonatan Halvardson3, Nicholas W Chavkin1,4, Ying Wang1, Miho Sano1, Jonas Mattisson3, Atsushi Hata5, Marcus Danielsson3, Emiri Miura-Yura1, Ammar Zaghlool3, Megan A Evans1, Tove Fall6, Henry N De Hoyos1, Johan Sundström7, Yoshimitsu Yura1, Anupreet Kour1, Yohei Arai1, Mark C Thel1, Yuka Arai1, Josyf C Mychaleckyj8, Karen K Hirschi4, Lars A Forsberg3,9, Kenneth Walsh1.
Abstract
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.Entities:
Keywords: clonal hematopoiesis
Mesh:
Substances:
Year: 2022 PMID: 35857592 PMCID: PMC9437978 DOI: 10.1126/science.abn3100
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 63.714