Department of Chemical Engineering, University of Washington, Seattle, WA 98195 (USA).
Angew Chem Int Ed Engl. 2014 Nov 17;53(47):12729-34. doi: 10.1002/anie.201405930. Epub 2014 Sep 22.
The success of human mesenchymal stem cell (hMSC) therapies is largely dependent on the ability to maintain the multipotency of cells and control their differentiation. External biochemical and biophysical cues can readily trigger hMSCs to spontaneously differentiate, thus resulting in a rapid decrease in the multipotent cell population and compromising their regenerative capacity. Herein, we demonstrate that nonfouling hydrogels composed of pure poly(carboxybetaine) (PCB) enable hMSCs to retain their stem-cell phenotype and multipotency, independent of differentiation-promoting media, cytoskeletal-manipulation agents, and the stiffness of the hydrogel matrix. Moreover, encapsulated hMSCs can be specifically induced to differentiate down osteogenic or adipogenic pathways by controlling the content of fouling moieties in the PCB hydrogel. This study examines the critical role of nonspecific interactions in stem-cell differentiation and highlights the importance of materials chemistry in maintaining stem-cell multipotency and controlling differentiation.
人类间充质干细胞(hMSC)疗法的成功在很大程度上取决于维持细胞多能性和控制其分化的能力。外部生化和生物物理线索可以轻易触发 hMSC 自发分化,从而导致多能细胞群体迅速减少,并损害其再生能力。本文中,我们证明了由纯聚(羧基甜菜碱)(PCB)组成的非固着水凝胶能够使 hMSC 保持其干细胞表型和多能性,而不受促分化培养基、细胞骨架操作剂和水凝胶基质的刚度的影响。此外,通过控制 PCB 水凝胶中固着基团的含量,可以特异性地诱导封装的 hMSC 向成骨或成脂途径分化。本研究考察了非特异性相互作用在干细胞分化中的关键作用,并强调了材料化学在维持干细胞多能性和控制分化中的重要性。