Optimization of physical microenvironment to maintain the quiescence of human induced pluripotent stem cell‐derived hepatic stellate cells

• Published in: Biotechnology and bioengineering 2023-08, Vol.120 (8), p.2345-2356
• Main Authors: Gong, Ya, Danoy, Mathieu, Kido, Taketomo, Mitsuhashi, Kento, Choi, Hyunjin, Matsugi, Tomoaki, Yang, Jingjing, Esashika, Katsuhiro, Takahashi, Jun, Nishikawa, Masaki, Ito, Taichi, Miyajima, Atsushi, Sakai, Yasuyuki
• Format: Article
• Language: English
• Subjects: Cell culture; Cell Differentiation; Culture; disease modeling; Extracellular matrix; Fibrosis; hepatic stellate cell; Hepatic Stellate Cells - metabolism; human induced pluripotent stem cell; Humans; Hydrogels; Induced Pluripotent Stem Cells - metabolism; Liver; Liver - metabolism; Liver Cirrhosis - metabolism; liver fibrosis; microenvironment; Microenvironments; Optimization; Pharmacology; Plastic plates; Pluripotency; quiescence; Stellate cells; Stem cells; Transforming growth factor-b1
• ISSN: 0006-3592; 1097-0290
• DOI: 10.1002/bit.28485

Hepatic stellate cells (HSCs) play a crucial role in liver fibrosis by producing excessive extracellular matrix (ECM) following chronic inflammation. However, studying HSC function has been challenging due to the limited availability of primary human quiescent HSCs (qHSCs) in vitro, and the fact that primary qHSCs quickly activate when cultured on plastic plates. Advances in stem cell technology have allowed for the generation of qHSCs from human induced pluripotent stem cells (hiPSCs) with the potential to provide an unlimited source of cells. However, differentiated quiescent‐like HSCs (iqHSCs) also activate spontaneously on conventional plastic plates. In this study, we generated iqHSCs from hiPSCs and developed a culture method to maintain such iqHSCs in a lowly activated state for up to 5 days by optimizing their physical culture microenvironment. We observed that three‐dimensional (3D) culture of iqHSCs in soft type 1 collagen hydrogels significantly inhibited their spontaneous activation in vitro while maintaining their ability to convert to activated state. Activation of iqHSC was successfully modeled by stimulating them with the fibrotic cytokine TGFβ1. Hence, our culture method can be used to generate HSCs with functions comparable to those in a healthy liver, facilitating the development of accurate in vitro liver models for identifying novel therapeutic agents.