诱导多能干细胞
类有机物
细胞培养
毒性
细胞毒性
干细胞
一氧化氮
活力测定
遗传毒性
彗星试验
细胞生物学
MTT法
化学
细胞凋亡
分子生物学
生物
体外
DNA损伤
生物化学
胚胎干细胞
基因
DNA
遗传学
有机化学
作者
Joo-Yeon Lee,Hyosin Baek,Jimin Jang,Jaehyun Park,Sang-Ryul Cha,Seok‐Ho Hong,Ji‐Eun Kim,Jong‐Hee Lee,In‐Sun Hong,Seung-Jun Wang,Ji Young Lee,Myung Ha Song,Se‐Ran Yang
标识
DOI:10.1016/j.tiv.2023.105585
摘要
Alveolar epithelial cells (AECs) are vulnerable to injury, which can result in epithelial hyperplasia, apoptosis, and chronic inflammation. In this study, we developed human induced pluripotent stem cell (hiPS) cell-derived AECs (iAECs) and the iAECs based organoids (AOs) for testing AEC toxicity after chemical exposure. HiPS cells were cultured for 14 days with differentiation medium corresponding to each step, and the iAECs-based AOs were maintained for another 14 days. SFTPC and AQP5 were expressed in the AOs, and mRNA levels of SOX9, NKX2.1, GATA6, HOPX, and ID2 were increased. The AOs were exposed for 24 h to nine chemical substances, and IC50 values of the nine chemicals were determined using MTT assay. When the correlations between iAECs 2D culture and AOs 3D culture were calculated using Pearson's correlation coefficient r value, the nine chemicals that caused a significant decrease of cell viability in 3D culture were found to be highly correlated in 2D culture. The cytotoxicity and nitric oxide release in AO cultured with macrophages were then investigated. When AOs with macrophages were exposed to sodium chromate for 24 h, the IC50 value and nitric oxide production were higher than when the AOs were exposed alone. Taken together, the AO-based 3D culture system provides a useful platform for understanding biological characteristics of AECs and modeling chemical exposures.
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