Eiken Madeline K, Levine Justin E, Lee Shinyeong, Lukpat Samantha, Plaster Eleanor M, Bala Vikram, Spence Jason R, Loebel Claudia
Department of Biomedical Engineering, University of Michigan, Carl A. Gerstacker Building, 2200 Bonisteel Blvd, Ann Arbor MI 48109, USA.
Department of Internal Medicine, Gastroenterology and Hepatology, University of Michigan Medical School, Taubman Center, 1500 East Medical Center Drive, Ann Arbor MI 48109, USA.
Adv Nanobiomed Res. 2025 Jan;5(1). doi: 10.1002/anbr.202300110. Epub 2024 Nov 21.
Bronchospheres have emerged as a promising in vitro model towards probing questions on organ development and disease. Several organoid models, including from airway (e.g., bronchial, tracheal) cells, require 3D Matrigel, a complex mouse tumor-derived matrix that typically leads to heterogenous size and structures. Synthetic and naturally-derived polymeric hydrogels show increased opportunities as an alternative to Matrigel culture. In addition, recent advances in hydrogel-based microcavities (i.e., microwells) have shown improved control over organoid size, structure, and composition. Here, we build upon this approach and describe the fabrication and characterization of microwell hydrogels based on other polymers, including diacrylated poly(ethylene glycol), agarose, methacrylated gelatin, and norbornene-modified hyaluronic acid. Using these microwell hydrogels, human bronchial epithelial cells and lung fibroblasts readily assemble into viable cyst-like bronchospheres. Our study shows that the cellular composition regulates the formation and structure of the bronchosphere which is also regulated by the type and adhesiveness of the hydrogel. Furthermore, both hydrogel type and cellular composition influence the amount and composition of deposited ECM within the microwells. This hydrogel fabrication platform provides an accessible in vitro culture platform for the formation and growth of bronchospheres which can be extended to the culture of other stem/progenitor and tissue-derived organoids.
支气管球已成为一种很有前景的体外模型,可用于探究器官发育和疾病相关问题。包括气道(如支气管、气管)细胞在内的几种类器官模型需要三维基质胶,这是一种复杂的源自小鼠肿瘤的基质,通常会导致大小和结构各异。合成和天然衍生的聚合物水凝胶作为基质胶培养的替代物,展现出更多机会。此外,基于水凝胶的微腔(即微孔)方面的最新进展表明,对类器官的大小、结构和组成有了更好的控制。在此,我们基于此方法进行拓展,描述了基于其他聚合物(包括二丙烯酸化聚乙二醇、琼脂糖、甲基丙烯酸化明胶和降冰片烯修饰的透明质酸)的微孔水凝胶的制备和表征。使用这些微孔水凝胶,人支气管上皮细胞和肺成纤维细胞很容易组装成有活力的囊状支气管球。我们的研究表明,细胞组成调节支气管球的形成和结构,而这也受水凝胶类型和黏附性的调节。此外,水凝胶类型和细胞组成都会影响微孔内沉积的细胞外基质的量和组成。这种水凝胶制备平台为支气管球的形成和生长提供了一个易于使用的体外培养平台,可扩展到其他干细胞/祖细胞和组织来源类器官的培养。