Eiken Madeline K, Childs Charlie J, Brastrom Lindy K, Frum Tristan, Plaster Eleanor M, Shachaf Orren, Pfeiffer Suzanne, Levine Justin E, Alysandratos Konstantinos-Dionysios, Kotton Darrell N, Spence Jason R, Loebel Claudia
Department of Biomedical Engineering, University of Michigan, Ann Arbor, USA.
Department of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI, USA.
bioRxiv. 2024 Mar 19:2024.03.19.585720. doi: 10.1101/2024.03.19.585720.
Human induced pluripotent stem cell (iPSC) derived alveolar organoids have emerged as a system to model the alveolar epithelium in homeostasis and disease. However, alveolar organoids are typically grown in Matrigel, a mouse-sarcoma derived basement membrane matrix that offers poor control over matrix properties, prompting the development of synthetic hydrogels as a Matrigel alternative. Here, we develop a two-step culture method that involves pre-aggregation of organoids in hydrogel-based microwells followed by embedding in a synthetic hydrogel that supports alveolar organoid growth, while also offering considerable control over organoid and hydrogel properties. We find that the aggregated organoids secrete their own nascent extracellular matrix (ECM) both in the microwells and upon embedding in the synthetic hydrogels. Thus, the synthetic gels described here allow us to de-couple exogenous and nascent ECM in order to interrogate the role of ECM in organoid formation.
人诱导多能干细胞(iPSC)衍生的肺泡类器官已成为一种在稳态和疾病中模拟肺泡上皮的系统。然而,肺泡类器官通常在基质胶中培养,基质胶是一种源自小鼠肉瘤的基底膜基质,对基质特性的控制较差,这促使人们开发合成水凝胶作为基质胶的替代品。在此,我们开发了一种两步培养方法,该方法包括在基于水凝胶的微孔中对类器官进行预聚集,然后嵌入支持肺泡类器官生长的合成水凝胶中,同时还能对类器官和水凝胶特性进行相当程度的控制。我们发现,聚集的类器官在微孔中和嵌入合成水凝胶后都会分泌自身的新生细胞外基质(ECM)。因此,本文所述的合成凝胶使我们能够分离外源性和新生的ECM,以便探究ECM在类器官形成中的作用。