Hematopoietic loss of Y chromosome leads to cardiac fibrosis and heart failure mortality

Author:

Sano Soichi12ORCID,Horitani Keita1,Ogawa Hayato1ORCID,Halvardson Jonatan3ORCID,Chavkin Nicholas W.14ORCID,Wang Ying1ORCID,Sano Miho1,Mattisson Jonas3ORCID,Hata Atsushi5ORCID,Danielsson Marcus3ORCID,Miura-Yura Emiri1ORCID,Zaghlool Ammar3,Evans Megan A.1,Fall Tove6ORCID,De Hoyos Henry N.1ORCID,Sundström Johan7ORCID,Yura Yoshimitsu1ORCID,Kour Anupreet1,Arai Yohei1,Thel Mark C.1,Arai Yuka1,Mychaleckyj Josyf C.8ORCID,Hirschi Karen K.4ORCID,Forsberg Lars A.39ORCID,Walsh Kenneth1ORCID

Affiliation:

1. Hematovascular Biology Center, Robert M. Berne Cardiovascular Research Center, University of Virginia School of Medicine, Charlottesville, VA 22908, USA.

2. Department of Cardiovascular Medicine, Osaka Metropolitan University Graduate School of Medicine, Osaka 545-8585, Japan.

3. Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, 75108 Uppsala, Sweden.

4. Department of Cell Biology, University of Virginia School of Medicine, Charlottesville, VA 22908, USA.

5. Chiba University Graduate School of Medicine, Department of General Thoracic Surgery, Chiba 260-8670, Japan.

6. Department of Medical Sciences, Molecular Epidemiology and Science for Life Laboratory, Uppsala University, 75185 Uppsala, Sweden.

7. Department of Medical Sciences, Uppsala University, Sweden, and Uppsala Clinical Research Center, 78185 Uppsala, Sweden.

8. Center for Public Health Genomics, University of Virginia, Charlottesville, VA 22908, USA.

9. The Beijer Laboratory, Uppsala University, 75185 Uppsala, Sweden.

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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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