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Immune Cell-Derived Exosomes in the Cancer-Immunity Cycle
被引:125
|作者:
Yan, Wei
[1
]
Jiang, Shuai
[2
]
机构:
[1] Wuhan Univ, Dept Cell Biol, Coll Life Sci, Wuhan 430072, Peoples R China
[2] Louisiana State Univ, Hlth Sci Ctr, Dept Microbiol & Immunol, Shreveport, LA 71130 USA
来源:
TRENDS IN CANCER
|
2020年
/
6卷
/
06期
关键词:
NANOPARTICLE TRACKING ANALYSIS;
IMAGING FLOW-CYTOMETRY;
DENDRITIC CELLS;
EXTRACELLULAR VESICLES;
IN-VITRO;
SECRETION;
DIFFERENTIATION;
SURVEILLANCE;
SUPPRESSION;
BIOGENESIS;
D O I:
10.1016/j.trecan.2020.02.013
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Cells can communicate through extracellular vesicle (EV) secretion and uptake. Exosomes are lipid bilayer-enclosed EVs of 30-150 nm in diameter, which can transfer RNA, functional proteins, lipids, and metabolites to recipient cells in vivo. Most cell types, including immune cells, can secrete and uptake exosomes. Biogenesis, secretion, and uptake of immune cell-derived exosomes are regulated by intracellular proteins and extracellular stimuli. Immune cell-derived exosomes can mediate crosstalk between innate and adaptive immunity and regulate cancer progression and metastasis. The dichotomous roles of immune cell-derived exosomes towards tumor cells can induce suppressive or active immune responses. Hence, immune cell-secreted exosomes may have applications in cancer diagnosis and immunotherapy and could potentially be developed for vaccination and chemotherapy drug transportation.
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页码:506 / 517
页数:12
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