Mechano-responsive hydrogel for direct stem cell manufacturing to therapy

被引:29
|
作者
Shou, Yufeng [1 ,2 ]
Liu, Ling [2 ,4 ]
Liu, Qimin [3 ]
Le, Zhicheng [1 ,2 ]
Lee, Khang Leng [5 ]
Li, Hua [6 ]
Li, Xianlei [1 ,2 ]
Koh, Dion Zhanyun [1 ]
Wang, Yuwen [1 ]
Liu, Tong Ming [7 ]
Yang, Zheng [4 ,8 ]
Lim, Chwee Teck [1 ,2 ,9 ]
Cheung, Christine [5 ,7 ]
Tay, Andy [1 ,2 ,4 ]
机构
[1] Natl Univ Singapore, Dept Biomed Engn, Singapore 117583, Singapore
[2] Natl Univ Singapore, Inst Hlth Innovat & Technol, Singapore 117599, Singapore
[3] Wuhan Univ Technol, Sch Civil Engn & Architecture, Wuhan 430070, Peoples R China
[4] Natl Univ Singapore, NUS Tissue Engn Program, Singapore 117510, Singapore
[5] Nanyang Technol Univ, Lee Kong Chian Sch Med, Singapore 636921, Singapore
[6] Nanyang Technol Univ, Sch Mech & Aerosp Engn, Singapore 639798, Singapore
[7] Inst Mol & Cell Biol, Agcy Sci Technol & Res ASTAR, Singapore 138648, Singapore
[8] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Orthopaed Surg, Singapore 119288, Singapore
[9] Natl Univ Singapore, Mechanobiol Inst, Singapore 117411, Singapore
关键词
Mesenchymal stem cell; Dynamic mechanical stimulation; Magnetic hydrogel; Stem cell manufacturing; Cell therapy; REGULATES ADHESION; DIFFERENTIATION; SHAPE; NANOPARTICLES; SURFACE; LIGAND; CYTOSKELETAL; VIABILITY; MOBILITY;
D O I
10.1016/j.bioactmat.2022.12.019
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Bone marrow-derived mesenchymal stem cell (MSC) is one of the most actively studied cell types due to its regenerative potential and immunomodulatory properties. Conventional cell expansion methods using 2D tissue culture plates and 2.5D microcarriers in bioreactors can generate large cell numbers, but they compromise stem cell potency and lack mechanical preconditioning to prepare MSC for physiological loading expected in vivo. To overcome these challenges, in this work, we describe a 3D dynamic hydrogel using magneto-stimulation for direct MSC manufacturing to therapy. With our technology, we found that dynamic mechanical stimulation (DMS) enhanced matrix-integrin beta 1 interactions which induced MSCs spreading and proliferation. In addition, DMS could modulate MSC biofunctions including directing MSC differentiation into specific lineages and boosting paracrine activities (e.g., growth factor secretion) through YAP nuclear localization and FAK-ERK pathway. With our magnetic hydrogel, complex procedures from MSC manufacturing to final clinical use, can be integrated into one single platform, and we believe this 'all-in-one' technology could offer a paradigm shift to existing standards in MSC therapy.
引用
收藏
页码:387 / 400
页数:14
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