Assembled/Disassembled Modular Scaffolds for Multicellular Tissue Engineering

Author:

Yu Xiaopeng12,Ma Hongshi12,Wang Yufeng1,Hao Jianxin12,Chen Lei12,Gelinsky Michael3,Wu Chengtie12ORCID

Affiliation:

1. State Key Laboratory of High Performance Ceramics and Superfine Microstructure Shanghai Institute of Ceramics Chinese Academy of Sciences Shanghai 200050 P. R. China

2. Center of Materials Science and Optoelectronics Engineering University of Chinese Academy of Sciences Beijing 100049 P. R. China

3. Center for Translational Bone Joint and Soft Tissue Research University Hospital Carl Gustav Carus and Faculty of Medicine of Dresden University of Technology Fetscherstr. 74 01307 Dresden Germany

Abstract

AbstractThe behavior of tissue resident cells can be influenced by the spatial arrangement of cellular interactions. Therefore, it is of significance to precisely control the spatial organization of various cells within multicellular constructs. It remains challenging to construct a versatile multicellular scaffold with ordered spatial organization of multiple cell types. Herein, a modular multicellular tissue engineering scaffold with ordered spatial distribution of different cell types is constructed by assembling varying cell‐laden modules. Interestingly, the modular scaffolds can be disassembled into individual modules to evaluate the specific contribution of each cell type in the system. Through assembling cell‐laden modules, the macrophage‐mesenchymal stem cell (MSC), endothelial cell‐MSC, and chondrocyte‐MSC co‐culture models are successfully established. The in vitro results indicate that the intercellular cross‐talk can promote the proliferation and differentiation of each cell type in the system. Moreover, MSCs in the modular scaffolds may regulate the behavior of chondrocytes through the nuclear factor of activated T‐Cells (NFAT) signaling pathway. Furthermore, the modular scaffolds loaded with co‐cultured chondrocyte‐MSC exhibit enhanced regeneration ability of osteochondral tissue, compared with other groups. Overall, this work offers a promising strategy to construct a multicellular tissue engineering scaffold for the systematic investigation of intercellular cross‐talk and complex tissue engineering.

Funder

National Natural Science Foundation of China

Science and Technology Commission of Shanghai Municipality

National Key Research and Development Program of China

Publisher

Wiley

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