Decellularized extracellular matrix mediates tissue construction and regeneration

Chuanqi Liu, Ming Pei, Qingfeng Li, Yuanyuan Zhang

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PDF(1299 KB)
Front. Med. ›› 2022, Vol. 16 ›› Issue (1) : 56-82. DOI: 10.1007/s11684-021-0900-3
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Decellularized extracellular matrix mediates tissue construction and regeneration

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Abstract

Contributing to organ formation and tissue regeneration, extracellular matrix (ECM) constituents provide tissue with three-dimensional (3D) structural integrity and cellular-function regulation. Containing the crucial traits of the cellular microenvironment, ECM substitutes mediate cell–matrix interactions to prompt stem-cell proliferation and differentiation for 3D organoid construction in vitro or tissue regeneration in vivo. However, these ECMs are often applied generically and have yet to be extensively developed for specific cell types in 3D cultures. Cultured cells also produce rich ECM, particularly stromal cells. Cellular ECM improves 3D culture development in vitro and tissue remodeling during wound healing after implantation into the host as well. Gaining better insight into ECM derived from either tissue or cells that regulate 3D tissue reconstruction or organ regeneration helps us to select, produce, and implant the most suitable ECM and thus promote 3D organoid culture and tissue remodeling for in vivo regeneration. Overall, the decellularization methodologies and tissue/cell-derived ECM as scaffolds or cellular-growth supplements used in cell propagation and differentiation for 3D tissue culture in vitro are discussed. Moreover, current preclinical applications by which ECM components modulate the wound-healing process are reviewed.

Keywords

decellularized extracellular matrix / 3D culture / organoids / tissue repair

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Chuanqi Liu, Ming Pei, Qingfeng Li, Yuanyuan Zhang. Decellularized extracellular matrix mediates tissue construction and regeneration. Front. Med., 2022, 16(1): 56‒82 https://doi.org/10.1007/s11684-021-0900-3

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Acknowledgements

We thank Ms. Suzanne Danley (Department of Orthopaedics, West Virginia University) for editing the manuscript. This work was partially supported by Research Grants from the National Institutes of Health (No. 1R01AR067747) to Ming Pei and by NIH/NIAID (Nos. R21AI152832 and R03AI165170) to Yuanyuan Zhang.

Compliance with ethics guidelines

Chuanqi Liu, Ming Pei, Qingfeng Li, and Yuanyuan Zhang declare that they have no conflict of interest. This manuscript is a review article and does not involve a research protocol requiring approval by the relevant institutional review board or ethics committee.

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