Macrophage engulfment of a cell or nanoparticle is regulated by unavoidable opsonization, a species-specific 'Marker of Self' CD47, and target physical properties

被引:79
作者
Sosale, Nisha G. [1 ]
Spinier, Kyle R. [1 ]
Alvey, Cory [1 ]
Discher, Dennis E. [1 ]
机构
[1] Univ Penn, Mol & Cell Biophys & NanoBioPolymers Labs, Philadelphia, PA 19104 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
RECEPTOR-MEDIATED PHAGOCYTOSIS; RED-BLOOD-CELLS; PROTEIN-ALPHA; MYOSIN-II; FC-GAMMA; DELIVERY; ENGRAFTMENT; CLEARANCE;
D O I
10.1016/j.coi.2015.06.013
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Professional phagocytes of the mononuclear phagocyte system (MPS), especially ubiquitous macrophages, are commonly thought to engulf or not a target based strictly on 'eat me' molecules such as Antibodies. The target might be a viable 'self' cell or a drug-delivering nanoparticle, or it might be a cancer cell or a microbe. 'Marker of Self' CD47 signals into a macrophage to inhibit the acto-myosin cytoskeleton that makes engulfment efficient. In adhesion of any cell, the same machinery is generally activated by rigidity of target surfaces, and recent results confirm phagocytosis is likewise driven by the rigidity typical of microbes and many synthetics. Basic insights are already being applied in order to make macrophages eat cancer or to delay nanoparticle clearance for better drug delivery and imaging.
引用
收藏
页码:107 / 112
页数:6
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