Intercellular trogocytosis plays an important role in modulation of immune responses

被引:97
作者
Ahmed, Khawaja Ashfaque [2 ,3 ]
Munegowda, Manjunatha Ankathatti [2 ,3 ]
Xie, Yufeng [2 ,3 ]
Xiang, Jim [1 ,2 ,3 ]
机构
[1] Univ Saskatchewan, Saskatoon Canc Ctr, Saskatchewan Canc Agcy, Res Unit,Dept Oncol,Coll Med, Saskatoon, SK S7N 4H4, Canada
[2] Univ Saskatchewan, Saskatchewan Canc Agcy, Dept Microbiol, Res Unit,Coll Med, Saskatoon, SK S7N 4H4, Canada
[3] Univ Saskatchewan, Saskatchewan Canc Agcy, Dept Immunol, Res Unit,Coll Med, Saskatoon, SK S7N 4H4, Canada
关键词
cellular interaction; membrane molecule transfer; CTL response; immune suppression;
D O I
10.1038/cmi.2008.32
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Intercellular communication is an important means of molecular information transfer through exchange of membrane proteins from cells to cells. Advent of the latest analytical and imaging tools has allowed us to enhance our understanding of the cellular communication through the intercellular exchange of intact membrane patches, also called trogocytosis, which is a ubiquitous phenomenon. Immune responses against pathogens or any foreign antigens require fine immune regulation, where cellular communications are mediated by either soluble or cell surface molecules. It has been demonstrated that the membrane molecule transfer between immune cells such as dendritic and T cells can be derived through internalization/recycling pathway, dissociation-associated pathway, uptake of exosomes and membrane nanotube formations. Recent evidence implicates the trogocytosis as an important mechanism of the immune system to modulate immune responses. Exchange of membrane molecules/antigens between immune cells has been observed for a long time, but the mechanisms and functional consequences of these transfers remain unclear. In this review, we discuss the possible mechanisms of trogocytosis and its physiological relevance to immune system, with special reference to T cells and the stimulatory or suppressive immune responses derived from T cells with acquired dendritic cell membrane molecules.
引用
收藏
页码:261 / 269
页数:9
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