Hematopoietic and eosinophil-specific LNK(SH2B3) deficiency promotes eosinophilia and arterial thrombosis.

Autor:	Dou H; Molecular Medicine, Columbia University Medical Center, New York, NY., Wang R; Molecular Medicine, Columbia University Medical Center, New York, NY., Tavallaie M; Molecular Medicine, Columbia University Medical Center, New York, NY., Xiao T; Molecular Medicine, Columbia University Medical Center, New York, NY., Olszewska M; Department of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY.; Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.; Black Family Stem Cell Institute, Icahn School of Medicine at Mount Sinai, New York, NY.; Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY.; Center for Advancement of Blood Cancer Therapies, Icahn School of Medicine at Mount Sinai, New York, NY., Papapetrou EP; Department of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY.; Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.; Black Family Stem Cell Institute, Icahn School of Medicine at Mount Sinai, New York, NY.; Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY.; Center for Advancement of Blood Cancer Therapies, Icahn School of Medicine at Mount Sinai, New York, NY., Tall AR; Molecular Medicine, Columbia University Medical Center, New York, NY., Wang N; Molecular Medicine, Columbia University Medical Center, New York, NY.
Jazyk:	angličtina
Zdroj:	Blood [Blood] 2024 Apr 25; Vol. 143 (17), pp. 1758-1772.
DOI:	10.1182/blood.2023021055
Abstrakt:	Abstract: Increased eosinophil counts are associated with cardiovascular disease and may be an independent predictor of major cardiovascular events. However, the causality and underlying mechanisms are poorly understood. Genome-wide association studies have shown an association of a common LNK variant (R262W, T allele) with eosinophilia and atherothrombotic disorders. LNK(TT) reduces LNK function, and Lnk-deficient mice display accelerated atherosclerosis and thrombosis. This study was undertaken to assess the role of eosinophils in arterial thrombosis in mice with hematopoietic Lnk deficiency. Hematopoietic Lnk deficiency increased circulating and activated eosinophils, JAK/STAT signaling in eosinophils, and carotid arterial thrombosis with increased eosinophil abundance and extracellular trap formation (EETosis) in thrombi. Depletion of eosinophils by anti-Siglec-F antibody or by the ΔdbIGata1 mutation eliminated eosinophils in thrombi and markedly reduced thrombosis in mice with hematopoietic Lnk deficiency but not in control mice. Eosinophil depletion reduced neutrophil abundance and NETosis in thrombi without altering circulating neutrophil counts. To assess the role of Lnk specifically in eosinophils, we crossed Lnkf/f mice with eoCre mice. LnkΔeos mice displayed isolated eosinophilia, increased eosinophil activation, and accelerated arterial thrombosis associated with increased EETosis and NETosis in thrombi. DNase I infusion abolished EETs and neutrophil extracellular traps (NETs) in thrombi and reversed the accelerated thrombosis. Human induced pluripotent stem cell-derived LNK(TT) eosinophils showed increased activation and EETosis relative to isogenic LNK(CC) eosinophils, demonstrating human relevance. These studies show a direct link between eosinophilia, EETosis, and atherothrombosis in hematopoietic Lnk deficiency and an essential role of eosinophil LNK in suppression of arterial thrombosis. (© 2024 American Society of Hematology. Published by Elsevier Inc. All rights are reserved, including those for text and data mining, AI training, and similar technologies.)
Databáze:	MEDLINE
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