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利用分子工程实现细胞间可逆相互作用的时空控制。

Spatiotemporal control of cell-cell reversible interactions using molecular engineering.

机构信息

Laboratory of Chemical Biology and State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China.

University of Chinese Academy of Sciences, Beijing 100039, China.

出版信息

Nat Commun. 2016 Oct 6;7:13088. doi: 10.1038/ncomms13088.

Abstract

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 β-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.

摘要

细胞间相互作用的调控在基础研究和基于细胞的治疗中有潜在的应用。在此,我们结合代谢糖基标记和生物正交点击反应,构建了带有β-环糊精的细胞膜,并通过光响应的主客体识别来操纵细胞行为。通过这种方法,我们证明了细胞组装和拆卸的可逆调控。与之前报道的不可逆效应相反,该方法能够实现光可控的细胞间黏附的可逆组装,在后者中,改变的结构不能重复使用。我们还通过设计基于细胞的治疗方法说明了该方法的实用性。经适体修饰的外周血单个核细胞被有效地重新导向靶细胞,导致细胞凋亡增强。我们的方法允许对可逆的细胞间相互作用进行精确控制,我们期望它将促进基于细胞的治疗的进一步发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f94b/5059747/298c145f4369/ncomms13088-f1.jpg

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