Spatiotemporal control of cell-cell reversible interactions using molecular engineering

被引:102
|
作者
Shi, Peng [1 ,2 ,3 ]
Ju, Enguo [1 ,2 ,3 ]
Yan, Zhengqing [1 ,2 ,3 ]
Gao, Nan [1 ,2 ]
Wang, Jiasi [1 ,2 ,3 ]
Hou, Jianwen [3 ]
Zhang, Yan [4 ]
Ren, Jinsong [1 ,2 ]
Qu, Xiaogang [1 ,2 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, Biol Chem Lab, Changchun 130022, Peoples R China
[2] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Rare Earth Resource Utilizat, Changchun 130022, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100039, Peoples R China
[4] Jilin Univ, Coll Iife Sci, Changchun 130012, Peoples R China
来源
NATURE COMMUNICATIONS | 2016年 / 7卷
关键词
CLICK CHEMISTRY; LIVE CELLS; ADHESION; DNA; SURFACES; DELIVERY; RELEASE; RECOGNITION; CAPTURE; GLYCANS;
D O I
10.1038/ncomms13088
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Manipulation of cell-cell interactions has potential applications in basic research and cell-based therapy. Herein, using a combination of metabolic glycan labelling and bio-orthogonal click reaction, we engineer cell membranes with beta-cyclodextrin and subsequently manipulate cell behaviours via photo-responsive host-guest recognition. With this methodology, we demonstrate reversible manipulation of cell assembly and disassembly. The method enables light-controllable reversible assembly of cell-cell adhesion, in contrast with previously reported irreversible effects, in which altered structure could not be reused. We also illustrate the utility of the method by designing a cell-based therapy. Peripheral blood mononuclear cells modified with aptamer are effectively redirected towards target cells, resulting in enhanced cell apoptosis. Our approach allows precise control of reversible cell-cell interactions and we expect that it will promote further developments of cell-based therapy.
引用
收藏
页数:9
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