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- W2140112018 endingPage "178" @default.
- W2140112018 startingPage "167" @default.
- W2140112018 abstract "Summary Monocytes are part of the vertebrate innate immune system. Blood monocytes are produced by bone marrow and splenic progenitors that derive from hematopoietic stem cells ( HSC s). In cardiovascular disease, such as atherosclerosis and myocardial infarction, HSC s proliferate at higher levels that in turn increase production of hematopoietic cells, including monocytes. Once produced in hematopoietic niches, monocytes intravasate blood vessels, circulate, and migrate to sites of inflammation. Monocyte recruitment to atherosclerotic plaque and the ischemic heart depends on various chemokines, such as CCL 2, CX 3 CL 1, and CCL 5. Once in tissue, monocytes can differentiate into macrophages and dendritic cells. Macrophages are end effector cells that regulate the steady state and tissue healing, but they can also promote disease. At sites of inflammation, monocytes and macrophages produce inflammatory cytokines, which can exacerbate disease progression. Macrophages can also phagocytose tissue debris and produce pro‐healing cytokines. Additionally, macrophages are antigen‐presenting cells and can prime T cells. The tissue environment, including cytokines and types of inflammation, instructs macrophage specialization. Understanding monocytosis and its consequences in disease will reveal new therapeutic opportunities without compromising steady state functions." @default.
- W2140112018 created "2016-06-24" @default.
- W2140112018 creator A5066332651 @default.
- W2140112018 creator A5078805078 @default.
- W2140112018 date "2014-10-15" @default.
- W2140112018 modified "2023-10-18" @default.
- W2140112018 title "Regulation and consequences of monocytosis" @default.
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