Bio-orthogonal click reaction-enabled highly specific in situ cellularization of tissue engineering scaffolds
Bio-orthogonal click reaction-enabled highly specific in situ cellularization of tissue engineering scaffolds
复制标题
生物正交点击反应使组织工程支架具有高度特异性的原位细胞化
DOI:
10.1016/j.biomaterials.2019.119615
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发表时间:
2020
期刊:
影响因子:
14
通讯作者:
Bin Liu
中科院分区:
文献类型:
--
作者:
Duo Mao;Chuangnian Zhang;Kenry;Jing Liu;Xiaoxiao Wang;Binhan Li;Hongyu Yan;Fang Hu;Deling Kong;Zhihong Wang;Bin Liu
Tissue engineering generally utilizes natural or synthetic scaffolds to repair or replace damaged tissues. However, due to the lack of guidance of biological signals, most of the implanted scaffolds have always suffered from poorin vivocellularization. Herein, we demonstrate a bio-orthogonal reaction-based strategy to realizein situspecific and fast cellularization of tissue engineering scaffold. DBCO-modified PCL-PEG (PCL-PEG-DBCO) polymer was synthesized and then fabricated into PCL-PEG-DBCO film through electrospinning. Meanwhile, azide-labeled macrophages (N3(+) macrophages) were obtained through metabolic glycoengineering. Through a series ofin vitrodynamic andin vivocharacterization, DBCO-modified films were noted to dramatically increase the selective capture efficiency and survival rate of N3(+) cells. Additionally, there is negligible influence of covalent conjugation on cell viability and proliferation, indicating the feasibility of the bio-orthogonal click reaction-based tissue engineering strategy. Overall, this work shows the advantages of anin situbio-orthogonal click reaction in realizing highly specific, efficient, and long-lasting scaffold cellularization. We anticipate that this general strategy would be widely applicable and useful in tissue engineering and regenerative medicine in the near future.