Putative Mechanisms Underlying Cardiovascular Disease Associated with Clonal Hematopoiesis of Indeterminate Potential

被引:4
作者
Burns, Sarah S. [1 ,2 ]
Kapur, Reuben [1 ,2 ,3 ,4 ]
机构
[1] Indiana Univ Sch Med, Dept Med & Mol Genet, Indianapolis, IN 46202 USA
[2] Indiana Univ Sch Med, Herman B Wells Ctr Pediat Res, Dept Pediat, Indianapolis, IN 46202 USA
[3] Indiana Univ Sch Med, Dept Microbiol & Immunol, Indianapolis, IN 46202 USA
[4] Indiana Univ Sch Med, Dept Mol Biol & Biochem, Indianapolis, IN 46202 USA
关键词
STEM-CELLS; MAST-CELLS; TET2; ATHEROSCLEROSIS; HEART; SURVIVORS; DNMT3A; CANCER; DIFFERENTIATION; INTERLEUKIN-1;
D O I
10.1016/j.stemcr.2020.06.021
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Characterized by the expansion of somatic mutations in the he-matopoietic lineages of aging individuals, clonal hematopoiesis of indeterminate potential (CHIP) is a common condition that in-creases the risk of developing hematological malignancies and car-diovascular disease (CVD). The presence of CHIP-associated muta-tions in hematopoietic stem and progenitor cells (HSPCs) suggests that these mutations may alter the functions of the diverse he-matopoietic lineages, many of which influence the pathogenesis of CVD. Inflammation may be a potential pathogenic mechanism, linking both CVD and hematological malignancy. However, it re-mains unknown whether CHIP-associated CVD and hematologi-cal malignancy are features of a common disease spectrum. The contributions of CHIP-associated mutations to both CVD and he-matological malignancy underscore the importance of stem cell biology in pathogenesis and treatment. This review discusses possible mechanisms underlying the contributions of multiple he-matopoietic lineages to CHIP-associated CVD and the putative pathogenic links between CHIP-associated CVD and hematologi-cal malignancy.
引用
收藏
页码:292 / 306
页数:15
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