CSF-1 Receptor Signaling in Myeloid Cells
Сигналинг рецептора CSF-1 в миелоидных клетках
2014-06-01
SCID: 54.1/eqm493wp
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CSF-1 receptorcolony-stimulating factor-1interleukin-34macrophage chemotaxistissue macrophages
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Abstract (AI)
The CSF-1 receptor (CSF-1R) is activated by the homodimeric growth factors colony-stimulating factor-1 (CSF-1) and interleukin-34 (IL-34). It plays important roles in development and in innate immunity by regulating the development of most tissue macrophages and osteoclasts, of Langerhans cells of the skin, of Paneth cells of the small intestine, and of brain microglia. It also regulates the differentiation of neural progenitor cells and controls functions of oocytes and trophoblastic cells in the female reproductive tract. Owing to this broad tissue expression pattern, it plays a central role in neoplastic, inflammatory, and neurological diseases. In this review we summarize the evolution, structure, and regulation of expression of the CSF-1R gene. We discuss the structures of CSF-1, IL-34, and the CSF-1R and the mechanism of ligand binding to and activation of the receptor. We further describe the pathways regulating macrophage survival, proliferation, differentiation, and chemotaxis downstream from the CSF-1R.
Key Findings
1
Because of its broad tissue expression, CSF-1R has central roles in neoplastic, inflammatory, and neurological diseases.
2
CSF-1R also regulates neural progenitor-cell differentiation and functions of oocytes and trophoblastic cells in the female reproductive tract.
3
CSF-1R is activated by the homodimeric growth factors CSF-1 and IL-34.
4
CSF-1R signaling regulates development of most tissue macrophages, osteoclasts, skin Langerhans cells, intestinal Paneth cells, and brain microglia.
5
Downstream CSF-1R pathways control macrophage survival, proliferation, differentiation, and chemotaxis.
Research Object
CSF-1 receptor (CSF-1R) signaling in myeloid cells
Research Subject
the structure, expression regulation, ligand binding and activation mechanisms, and downstream control of macrophage survival, proliferation, differentiation, and chemotaxis
Publication Details
Publication Date
2014-06-01
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