Putting the brakes on phagocytosis: "don't-eat-me" signaling in physiology and disease

被引:68
作者
Kelley, Shannon M. [1 ,2 ]
Ravichandran, Kodi S. [1 ,2 ,3 ]
机构
[1] Univ Virginia, Ctr Cell Clearance, Charlottesville, VA 22904 USA
[2] Univ Virginia, Dept Microbiol Immunol & Canc Biol, Charlottesville, VA 22904 USA
[3] Univ Ghent, Dept Biomed Mol Biol, VIB UGent Ctr Inflammat Res, Ghent, Belgium
关键词
‘ don' t‐ eat‐ me’ anti‐ phagocytic receptor; efferocytosis; ITIM; phagocytosis; PROTEIN-TYROSINE-PHOSPHATASE; INTEGRIN-ASSOCIATED PROTEIN; MHC CLASS-I; ALPHA SIRP-ALPHA; ALVEOLAR MACROPHAGE PHAGOCYTOSIS; RECEPTOR-MEDIATED PHAGOCYTOSIS; AUTOIMMUNE HEMOLYTIC-ANEMIA; HEMATOPOIETIC STEM-CELLS; REGULATES FC-GAMMA; APOPTOTIC CELLS;
D O I
10.15252/embr.202152564
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Timely removal of dying or pathogenic cells by phagocytes is essential to maintaining host homeostasis. Phagocytes execute the clearance process with high fidelity while sparing healthy neighboring cells, and this process is at least partially regulated by the balance of "eat-me" and "don't-eat-me" signals expressed on the surface of host cells. Upon contact, eat-me signals activate "pro-phagocytic" receptors expressed on the phagocyte membrane and signal to promote phagocytosis. Conversely, don't-eat-me signals engage "anti-phagocytic" receptors to suppress phagocytosis. We review the current knowledge of don't-eat-me signaling in normal physiology and disease contexts where aberrant don't-eat-me signaling contributes to pathology.
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页数:17
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