基质凝胶
类有机物
自愈水凝胶
祖细胞
诱导多能干细胞
细胞生物学
移植
再生医学
材料科学
干细胞
组织工程
细胞培养
透明质酸
纳米技术
细胞
生物
生物医学工程
解剖
胚胎干细胞
生物化学
医学
外科
高分子化学
遗传学
基因
作者
Claudia Loebel,Aaron I. Weiner,Madeline K. Eiken,Jeremy Katzen,Michael Morley,Vikram Bala,Fabian L. Cardenas-Diaz,Matthew D. Davidson,Kazushige Shiraishi,Maria C. Basil,Laura Ferguson,Jason R. Spence,Matthias Ochs,Michael F. Beers,Edward E. Morrisey,Andrew E. Vaughan,Jason A. Burdick
标识
DOI:10.1002/adma.202202992
摘要
Epithelial cell organoids have increased opportunities to probe questions on tissue development and disease in vitro and for therapeutic cell transplantation. Despite their potential, current protocols to grow these organoids almost exclusively depend on culture within 3D Matrigel, which limits defined culture conditions, introduces animal components, and results in heterogenous organoids (i.e., shape, size, composition). Here, a method is described that relies on hyaluronic acid hydrogels for the generation and expansion of lung alveolar organoids (alveolospheres). Using synthetic hydrogels with defined chemical and physical properties, human-induced pluripotent stem cell (iPSC)-derived alveolar type 2 cells (iAT2s) self-assemble into alveolospheres and propagate in Matrigel-free conditions. By engineering predefined microcavities within these hydrogels, the heterogeneity of alveolosphere size and structure is reduced when compared to 3D culture, while maintaining the alveolar type 2 cell fate of human iAT2-derived progenitor cells. This hydrogel system is a facile and accessible system for the culture of iPSC-derived lung progenitors and the method can be expanded to the culture of primary mouse tissue derived AT2 and other epithelial progenitor and stem cell aggregates.
科研通智能强力驱动
Strongly Powered by AbleSci AI