A disheartening loss
Although the Y chromosome is the smallest and contains few genes, its functions are not fully understood. It has been observed, however, that mosaic loss of the Y chromosome in blood cells frequently occurs with age, and this alteration is associated with various medical conditions. Sano et al. modeled this process in mice by reconstituting their bone marrow with cells lacking the Y chromosome (see the Perspective by Zeiher and Braun). The resulting mice were prone to fibrosis and decreased cardiac function, especially in the setting of pressure overload, but they benefited from treatment with a transforming growth factor β1–neutralizing antibody. Human patients with loss of chromosome Y in their blood were also at greater risk of cardiac pathology, supporting the clinical relevance of these findings. —YN
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.
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References and Notes
1
M. A. Jobling, C. Tyler-Smith, Human Y-chromosome variation in the genome-sequencing era. Nat. Rev. Genet. 18, 485–497 (2017).
2
L. A. Forsberg, C. Rasi, N. Malmqvist, H. Davies, S. Pasupulati, G. Pakalapati, J. Sandgren, T. Diaz de Ståhl, A. Zaghlool, V. Giedraitis, L. Lannfelt, J. Score, N. C. P. Cross, D. Absher, E. T. Janson, C. M. Lindgren, A. P. Morris, E. Ingelsson, L. Lind, J. P. Dumanski, Mosaic loss of chromosome Y in peripheral blood is associated with shorter survival and higher risk of cancer. Nat. Genet. 46, 624–628 (2014).
3
J. P. Dumanski, C. Rasi, M. Lönn, H. Davies, M. Ingelsson, V. Giedraitis, L. Lannfelt, P. K. E. Magnusson, C. M. Lindgren, A. P. Morris, D. Cesarini, M. Johannesson, E. Tiensuu Janson, L. Lind, N. L. Pedersen, E. Ingelsson, L. A. Forsberg, Smoking is associated with mosaic loss of chromosome Y. Science 347, 81–83 (2015).
4
D. J. Thompson, G. Genovese, J. Halvardson, J. C. Ulirsch, D. J. Wright, C. Terao, O. B. Davidsson, F. R. Day, P. Sulem, Y. Jiang, M. Danielsson, H. Davies, J. Dennis, M. G. Dunlop, D. F. Easton, V. A. Fisher, F. Zink, R. S. Houlston, M. Ingelsson, S. Kar, N. D. Kerrison, B. Kinnersley, R. P. Kristjansson, P. J. Law, R. Li, C. Loveday, J. Mattisson, S. A. McCarroll, Y. Murakami, A. Murray, P. Olszewski, E. Rychlicka-Buniowska, R. A. Scott, U. Thorsteinsdottir, I. Tomlinson, B. T. Moghadam, C. Turnbull, N. J. Wareham, D. F. Gudbjartsson, Y. Kamatani, E. R. Hoffmann, S. P. Jackson, K. Stefansson, A. Auton, K. K. Ong, M. J. Machiela, P.-R. Loh, J. P. Dumanski, S. J. Chanock, L. A. Forsberg, J. R. B. Perry; International Lung Cancer Consortium (INTEGRAL-ILCCO); Breast Cancer Association Consortium; Consortium of Investigators of Modifiers of BRCA1/2; Endometrial Cancer Association Consortium; Ovarian Cancer Association Consortium; Prostate Cancer Association Group to Investigate Cancer Associated Alterations in the Genome (PRACTICAL) Consortium; Kidney Cancer GWAS Meta-Analysis Project; eQTLGen Consortium; Biobank-based Integrative Omics Study (BIOS) Consortium; 23andMe Research Team, Genetic predisposition to mosaic Y chromosome loss in blood. Nature 575, 652–657 (2019).
5
V. Ljungström, J. Mattisson, J. Halvardson, T. Pandzic, H. Davies, E. Rychlicka-Buniowska, M. Danielsson, P. Lacaze, L. Cavelier, J. P. Dumanski, P. Baliakas, L. A. Forsberg, Loss of Y and clonal hematopoiesis in blood-two sides of the same coin?Leukemia 36, 889–891 (2022).
6
F. Zink, S. N. Stacey, G. L. Norddahl, M. L. Frigge, O. T. Magnusson, I. Jonsdottir, T. E. Thorgeirsson, A. Sigurdsson, S. A. Gudjonsson, J. Gudmundsson, J. G. Jonasson, L. Tryggvadottir, T. Jonsson, A. Helgason, A. Gylfason, P. Sulem, T. Rafnar, U. Thorsteinsdottir, D. F. Gudbjartsson, G. Masson, A. Kong, K. Stefansson, Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly. Blood 130, 742–752 (2017).
7
L. A. Forsberg, J. Halvardson, E. Rychlicka-Buniowska, M. Danielsson, B. T. Moghadam, J. Mattisson, C. Rasi, H. Davies, L. Lind, V. Giedraitis, L. Lannfelt, L. Kilander, M. Ingelsson, J. P. Dumanski, Mosaic loss of chromosome Y in leukocytes matters. Nat. Genet. 51, 4–7 (2019).
8
E. Loftfield, W. Zhou, B. I. Graubard, M. Yeager, S. J. Chanock, N. D. Freedman, M. J. Machiela, Predictors of mosaic chromosome Y loss and associations with mortality in the UK Biobank. Sci. Rep. 8, 12316 (2018).
9
J. P. Dumanski, J.-C. Lambert, C. Rasi, V. Giedraitis, H. Davies, B. Grenier-Boley, C. M. Lindgren, D. Campion, C. Dufouil, F. Pasquier, P. Amouyel, L. Lannfelt, M. Ingelsson, L. Kilander, L. Lind, L. A. Forsberg; European Alzheimer’s Disease Initiative Investigators, Mosaic loss of chromosome Y in blood is associated with Alzheimer Disease. Am. J. Hum. Genet. 98, 1208–1219 (2016).
10
S. Haitjema, D. Kofink, J. van Setten, S. W. van der Laan, A. H. Schoneveld, J. Eales, M. Tomaszewski, S. C. A. de Jager, G. Pasterkamp, F. W. Asselbergs, H. M. den Ruijter, Loss of Y chromosome in blood is associated with major cardiovascular events during follow-up in men after carotid endarterectomy. Circ. Cardiovasc. Genet. 10, e001544 (2017).
11
S. Sano, Y. Wang, M. A. Evans, Y. Yura, M. Sano, H. Ogawa, K. Horitani, H. Doviak, K. Walsh, Lentiviral CRISPR/Cas9-mediated genome editing for the study of hematopoietic cells in disease models. J. Vis. Exp. ( 152): (2019).
12
J. P. Dumanski, J. Halvardson, H. Davies, E. Rychlicka-Buniowska, J. Mattisson, B. T. Moghadam, N. Nagy, K. Węglarczyk, K. Bukowska-Strakova, M. Danielsson, P. Olszewski, A. Piotrowski, E. Oerton, A. Ambicka, M. Przewoźnik, Ł. Bełch, T. Grodzicki, P. L. Chłosta, S. Imreh, V. Giedraitis, L. Kilander, J. Nordlund, A. Ameur, U. Gyllensten, Å. Johansson, A. Józkowicz, M. Siedlar, A. Klich-Rączka, J. Jaszczyński, S. Enroth, J. Baran, M. Ingelsson, J. R. B. Perry, J. Ryś, L. A. Forsberg, Immune cells lacking Y chromosome show dysregulation of autosomal gene expression. Cell. Mol. Life Sci. 78, 4019–4033 (2021).
13
D. C. Rockey, P. D. Bell, J. A. Hill, Fibrosis—A common pathway to organ injury and failure. N. Engl. J. Med. 372, 1138–1149 (2015).
14
J. M. Daley, A. A. Thomay, M. D. Connolly, J. S. Reichner, J. E. Albina, Use of Ly6G-specific monoclonal antibody to deplete neutrophils in mice. J. Leukoc. Biol. 83, 64–70 (2008).
15
A. J. Rhee, K. J. Lavine, New approaches to target inflammation in heart failure: Harnessing insights from studies of immune cell diversity. Annu. Rev. Physiol. 82, 1–20 (2020).
16
Y. Wang, S. Sano, Y. Yura, Z. Ke, M. Sano, K. Oshima, H. Ogawa, K. Horitani, K.-D. Min, E. Miura-Yura, A. Kour, M. A. Evans, M. A. Zuriaga, K. K. Hirschi, J. J. Fuster, E. M. Pietras, K. Walsh, Tet2-mediated clonal hematopoiesis in nonconditioned mice accelerates age-associated cardiac dysfunction. JCI Insight 5, e135204 (2020).
17
L. Dorsheimer, B. Assmus, T. Rasper, C. A. Ortmann, A. Ecke, K. Abou-El-Ardat, T. Schmid, B. Brüne, S. Wagner, H. Serve, J. Hoffmann, F. Seeger, S. Dimmeler, A. M. Zeiher, M. A. Rieger, Association of mutations contributing to clonal hematopoiesis with prognosis in chronic ischemic heart failure. JAMA Cardiol. 4, 25–33 (2019).
18
B. Yu, M. B. Roberts, L. M. Raffield, S. M. Zekavat, N. Q. H. Nguyen, M. L. Biggs, M. R. Brown, G. Griffin, P. Desai, A. Correa, A. C. Morrison, A. M. Shah, A. Niroula, M. M. Uddin, M. C. Honigberg, B. L. Ebert, B. M. Psaty, E. A. Whitsel, J. E. Manson, C. Kooperberg, A. G. Bick, C. M. Ballantyne, A. P. Reiner, P. Natarajan, C. B. Eaton; National Heart, Lung, and Blood Institute TOPMed Consortium, Supplemental association of clonal hematopoiesis with incident heart failure. J. Am. Coll. Cardiol. 78, 42–52 (2021).
19
J. J. Fuster, S. MacLauchlan, M. A. Zuriaga, M. N. Polackal, A. C. Ostriker, R. Chakraborty, C.-L. Wu, S. Sano, S. Muralidharan, C. Rius, J. Vuong, S. Jacob, V. Muralidhar, A. A. B. Robertson, M. A. Cooper, V. Andrés, K. K. Hirschi, K. A. Martin, K. Walsh, Clonal hematopoiesis associated with TET2 deficiency accelerates atherosclerosis development in mice. Science 355, 842–847 (2017).
20
S. Sano, K. Oshima, Y. Wang, Y. Katanasaka, M. Sano, K. Walsh, CRISPR-mediated gene editing to assess the roles of Tet2 and Dnmt3a in clonal hematopoiesis and cardiovascular disease. Circ. Res. 123, 335–341 (2018).
21
S. Sano, K. Oshima, Y. Wang, S. MacLauchlan, Y. Katanasaka, M. Sano, M. A. Zuriaga, M. Yoshiyama, D. Goukassian, M. A. Cooper, J. J. Fuster, K. Walsh, Tet2-mediated clonal hematopoiesis accelerates heart failure through a mechanism involving the IL-1beta/NLRP3 inflammasome. J. Am. Coll. Cardiol. 71, 875–886 (2018).
22
Y. Yura, E. Miura-Yura, Y. Katanasaka, K.-D. Min, N. Chavkin, A. H. Polizio, H. Ogawa, K. Horitani, H. Doviak, M. A. Evans, M. Sano, Y. Wang, K. Boroviak, G. Philippos, A. F. Domingues, G. Vassiliou, S. Sano, K. Walsh, The cancer therapy-related clonal hematopoiesis driver gene Ppm1d promotes inflammation and non-ischemic heart failure in mice. Circ. Res. 129, 684–698 (2021).
23
M. Wijsenbeek, V. Cottin, Spectrum of fibrotic lung diseases. N. Engl. J. Med. 383, 958–968 (2020).
24
T. E. King Jr., W. Z. Bradford, S. Castro-Bernardini, E. A. Fagan, I. Glaspole, M. K. Glassberg, E. Gorina, P. M. Hopkins, D. Kardatzke, L. Lancaster, D. J. Lederer, S. D. Nathan, C. A. Pereira, S. A. Sahn, R. Sussman, J. J. Swigris, P. W. Noble; ASCEND Study Group, A phase 3 trial of pirfenidone in patients with idiopathic pulmonary fibrosis. N. Engl. J. Med. 370, 2083–2092 (2014).
25
G. A. Lewis, S. Dodd, D. Clayton, E. Bedson, H. Eccleson, E. B. Schelbert, J. H. Naish, B. D. Jimenez, S. G. Williams, C. Cunnington, F. Z. Ahmed, A. Cooper, S. Rajavarma Viswesvaraiah, S. Russell, T. McDonagh, P. R. Williamson, C. A. Miller, Pirfenidone in heart failure with preserved ejection fraction: A randomized phase 2 trial. Nat. Med. 27, 1477–1482 (2021).
26
A. Fujiwara, S. Funaki, E. Fukui, K. Kimura, T. Kanou, N. Ose, M. Minami, Y. Shintani, Effects of pirfenidone targeting the tumor microenvironment and tumor-stroma interaction as a novel treatment for non-small cell lung cancer. Sci. Rep. 10, 10900 (2020).
27
H. Aghajanian, T. Kimura, J. G. Rurik, A. S. Hancock, M. S. Leibowitz, L. Li, J. Scholler, J. Monslow, A. Lo, W. Han, T. Wang, K. Bedi, M. P. Morley, R. A. Linares Saldana, N. A. Bolar, K. McDaid, C.-A. Assenmacher, C. L. Smith, D. Wirth, C. H. June, K. B. Margulies, R. Jain, E. Puré, S. M. Albelda, J. A. Epstein, Targeting cardiac fibrosis with engineered T cells. Nature 573, 430–433 (2019).
28
F. Adikusuma, N. Williams, F. Grutzner, J. Hughes, P. Thomas, Targeted deletion of an entire chromosome using CRISPR/Cas9. Mol. Ther. 25, 1736–1738 (2017).
29
M. Riaz, J. Mattisson, G. Polekhina, A. Bakshi, J. Halvardson, M. Danielsson, A. Ameur, J. McNeil, L. A. Forsberg, P. Lacaze, A polygenic risk score predicts mosaic loss of chromosome Y in circulating blood cells. Cell Biosci. 11, 205 (2021).
30
M. Danielsson, J. Halvardson, H. Davies, B. Torabi Moghadam, J. Mattisson, E. Rychlicka-Buniowska, J. Jaszczyński, J. Heintz, L. Lannfelt, V. Giedraitis, M. Ingelsson, J. P. Dumanski, L. A. Forsberg, Longitudinal changes in the frequency of mosaic chromosome Y loss in peripheral blood cells of aging men varies profoundly between individuals. Eur. J. Hum. Genet. 28, 349–357 (2020).