骨髓
血管生成
髓样
造血
医学
白细胞增多症
造血干细胞
免疫学
内皮功能障碍
动脉发生
内皮干细胞
癌症研究
生物
病理
干细胞
内科学
细胞生物学
体外
生物化学
作者
David Rohde,Katrien Vandoorne,I‐Hsiu Lee,Jana Grune,Shuang Zhang,Cameron S. McAlpine,Maximilian J. Schloss,Ribhu Nayar,Gabriel Courties,Vanessa Frodermann,Gregory R. Wojtkiewicz,Lisa Honold,Qi Chen,Stephen Schmidt,Yoshiko Iwamoto,Yuan Sun,Sebastian Cremer,Friedrich Felix Hoyer,Oriol Iborra‐Egea,Christian Muñoz-Guijosa
标识
DOI:10.1038/s44161-021-00002-8
摘要
Abnormal hematopoiesis advances cardiovascular disease by generating excess inflammatory leukocytes that attack the arteries and the heart. The bone marrow niche regulates hematopoietic stem cell proliferation and hence the systemic leukocyte pool, but whether cardiovascular disease affects the hematopoietic organ's microvasculature is unknown. Here we show that hypertension, atherosclerosis and myocardial infarction (MI) instigate endothelial dysfunction, leakage, vascular fibrosis and angiogenesis in the bone marrow, altogether leading to overproduction of inflammatory myeloid cells and systemic leukocytosis. Limiting angiogenesis with endothelial deletion of
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