AI Article Synopsis
- - Human pluripotent stem cells (hPSCs), which include human embryonic and induced pluripotent stem cells, have unlimited growth potential, unlike adult stem cells that face aging issues.
- - Culturing hPSCs requires specific materials and surfaces, avoiding traditional plastic dishes used for adult stem cells, to ensure they can grow without feeder layers while maintaining their ability to differentiate into various cell types.
- - The review highlights various biomaterials, such as recombinant ECM proteins and advanced synthetic surfaces, that support hPSC growth under xeno-free conditions, reducing the risk of contamination and enhancing their clinical applications.
Article Abstract
Human pluripotent stem cells (human embryonic stem cells (hESCs) and induced pluripotent stem cells (hiPSCs)) have unlimited proliferative potential, whereas adult stem cells such as bone marrow-derived stem cells and adipose-derived stem cells have problems with aging. When hPSCs are intended to be cultured on feeder-free or xeno-free conditions without utilizing mouse embryonic fibroblasts or human fibroblasts, they cannot be cultured on conventional tissue culture polystyrene dishes, as adult stem cells can be cultured but should be cultivated on material surfaces grafted or coated with (a) natural or recombinant extracellular matrix (ECM) proteins, (b) ECM protein-derived peptides and specific synthetic polymer surfaces in xeno-free and/or chemically defined conditions. This review describes current developing cell culture biomaterials for the proliferation of hPSCs while maintaining the pluripotency and differentiation potential of the cells into 3 germ layers. Biomaterials for the cultivation of hPSCs without utilizing a feeder layer are essential to decrease the risk of xenogenic molecules, which contributes to the potential clinical usage of hPSCs. ECM proteins such as human recombinant vitronectin, laminin-511 and laminin-521 have been utilized instead of Matrigel for the feeder-free cultivation of hPSCs. The following biomaterials are also discussed for hPSC cultivation: (a) decellularized ECM, (b) peptide-grafted biomaterials derived from ECM proteins, (c) recombinant E-cadherin-coated surface, (d) polysaccharide-immobilized surface, (e) synthetic polymer surfaces with and without bioactive sites, (f) thermoresponsive polymer surfaces with and without bioactive sites, and (g) synthetic microfibrous scaffolds.
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| http://dx.doi.org/10.1016/bs.pmbts.2023.02.008 | DOI Listing |
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