期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 134, 期 38, 页码 15716-15719出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja307717w
关键词
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资金
- U.S. National Science Foundation [CBET-1033212]
- Connecticut Department of Public Health [09SCAUCON02]
- China Scholarship Council
- Directorate For Engineering
- Div Of Chem, Bioeng, Env, & Transp Sys [1340173] Funding Source: National Science Foundation
The ability to regulate cell material interactions is important in various applications such as regenerative medicine and cell separation. This study successfully demonstrates that the binding states of cells on a hydrogel surface can be programmed by using hybridized aptamers and triggering complementary sequences (CSs). In the absence of the triggering CSs, the aptamers exhibit a stable, hybridized state in the hydrogel for cell-type-specific catch. In the presence of the triggering CSs, the aptamers are transformed into a new hybridized state that leads to the rapid dissociation of the aptamers from the hydrogel. As a result, the cells are released from the hydrogel. The entire procedure of cell catch and release during the transformation of the aptamers is biocompatible and does not involve any factor destructive to either the cells or the hydrogel. Thus, the programmable hydrogel is regenerable and can be applied to a new round of cell catch and release when needed.
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