| Literature DB >> 30685690 |
Jianmin Yang1, Yingjun Yang2, Naoki Kawazoe2, Guoping Chen3.
Abstract
Cell delivery in cell therapy is typically challenged by the low cell survival rate and immunological rejection during cells injection and circulation. Encapsulation of cells with semipermeable hydrogels or membranes can improve cell viability by resisting high shear force and inhibit immune response with the physical isolation effect. Herein, the individual HeLa cells and human mesenchymal stem cells (hMSCs) were encapsulated with enzyme responsive polymer nanoshell. The encapsulation shell was prepared via the Layer-by-Layer (LbL) assembly of functionalized gelatin and click chemistry of peptide linker and gelatin. The encapsulated cells showed high cell viability and could resist the physical stress. Moreover, the encapsulation shell had a prolonged encapsulation sustaining period and could effectively prevent the invasion of external entities. In addition, on-site cell release was realized via enzymolysis of the encapsulation shell by human matrix metalloproteinase-7 (MMP-7), an overexpressed enzyme on tumor area. The finding of this study proved a potential approach in cell therapy, especially for cell-based cancer therapy.Entities:
Keywords: Cell encapsulation; Cell therapy; Enzyme responsive polymer; Individual cell; Nanoshell
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Year: 2019 PMID: 30685690 DOI: 10.1016/j.biomaterials.2019.01.029
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479