Exosomes and communication between tumours and the immune system: are all exosomes equal?

被引:104
作者
Bobrie, Angelique [1 ,2 ,3 ]
Thery, Clotilde [1 ,2 ]
机构
[1] Inst Curie, Sect Rech, F-75005 Paris, France
[2] INSERM, U932, F-75005 Paris, France
[3] Univ Paris 05, F-75006 Paris, France
关键词
exosome; extracellular vesicle; milk fat globule-epidermal growth factor-Factor VIII protein (Mfge8); Rab27a; tumour immunity; CELL-DERIVED EXOSOMES; MEMBRANE-VESICLES; B-LYMPHOCYTES; RESPONSES; ANTIGEN; MICROVESICLES; SECRETION; PROTEINS; CANCER; PROGRESSION;
D O I
10.1042/BST20120245
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Communication between cells is particularly important during tumour progression. Communication can take place through direct cell-cell interactions, but also through extracellular secretion of mediators acting at a distance. These mediators can be either soluble molecules or more complex structures called membrane vesicles, enclosing soluble factors within a lipid bilayer. A variety of extracellular membrane vesicles have been described, for instance microvesicles, ectosomes and a subtype called exosomes. The role of exosomes in tumour progression has been studied extensively in the last 10 years. In the present mini-review, we discuss our recent results, first showing the heterogeneity of the vesicles called exosomes and the probable existence of subpopulations of these exosomes, and secondly demonstrating that in vivo secretion of exosomes by some tumours can promote tumour progression, but that such a function cannot be generalized to all tumours and all exosomes.
引用
收藏
页码:263 / 267
页数:5
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