Department of Pharmacological and Biomolecular Sciences, The University of Milan, Italy.
Medical Biochemistry, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Pharmacol Res. 2021 Jul;169:105663. doi: 10.1016/j.phrs.2021.105663. Epub 2021 May 9.
Recruitment of innate immune cells and their accumulation in the arterial wall and infarcted myocardium has been recognized as a central feature of atherosclerosis and cardiac ischemic injury, respectively. In both, steady state and under pathological conditions, majority of these cells have a finite life span and are continuously replenished from haematopoietic stem/progenitor cell pool residing in the bone marrow and extramedullary sites. While having a crucial role in the cardiovascular disease development, proliferation and differentiation of innate immune cells within haematopoietic compartments is greatly affected by the ongoing cardiovascular pathology. In the current review, we summarize key cells, processes and tissue compartments that are involved in myelopoiesis under the steady state, during atherosclerosis development and in myocardial infarction.
先天免疫细胞在动脉壁和梗死心肌中的募集和积累分别被认为是动脉粥样硬化和心脏缺血损伤的核心特征。在这两种情况下,稳态下和病理条件下,这些细胞中的大多数都有一个有限的寿命,并从骨髓和骨髓外部位的造血干细胞/祖细胞池中不断得到补充。虽然先天免疫细胞在心血管疾病的发展中起着至关重要的作用,但造血细胞中的增殖和分化受到持续的心血管病理的极大影响。在这篇综述中,我们总结了稳态下、动脉粥样硬化发展过程中和心肌梗死后参与骨髓生成的关键细胞、过程和组织区室。