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源自人类肿瘤的外泌体与源自树突状细胞的外泌体具有不同的生物学作用和分子特征。

Human tumor-derived vs dendritic cell-derived exosomes have distinct biologic roles and molecular profiles.

作者信息

Wieckowski Eva, Whiteside Theresa L

机构信息

Departments of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.

出版信息

Immunol Res. 2006;36(1-3):247-54. doi: 10.1385/IR:36:1:247.

Abstract

Microvesicles (MV) or exosomes are produced and secreted by tumor and normal cells. The molecular profile and functions of tumor-derived vs dendritic cell (DC)-derived MV are distinct. The former express death ligands and mediate apoptosis of activated T cells. The latter promote CD4+ T cell proliferation and may play a role in regulating T cell responses. Serving as intercellular communication networks, tumor-derived MV contribute to tumor escape, while DC-derived MV drive and regulate immune response.

摘要

微泡(MV)或外泌体由肿瘤细胞和正常细胞产生并分泌。肿瘤来源的MV与树突状细胞(DC)来源的MV在分子特征和功能上有所不同。前者表达死亡配体并介导活化T细胞的凋亡。后者促进CD4+ T细胞增殖,并可能在调节T细胞反应中发挥作用。作为细胞间通讯网络,肿瘤来源的MV有助于肿瘤逃逸,而DC来源的MV驱动并调节免疫反应。

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