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  • 标题:Establishment of a developmental toxicity assay based on human iPSC reporter to detect FGF signal disruption
  • 本地全文:下载
  • 作者:Seiya Kanno ; Yusuke Okubo ; Tatsuto Kageyama
  • 期刊名称:iScience
  • 印刷版ISSN:2589-0042
  • 出版年度:2022
  • 卷号:25
  • 期号:2
  • 页码:1-20
  • DOI:10.1016/j.isci.2022.103770
  • 语种:English
  • 出版社:Elsevier
  • 摘要:SummaryThe number of man-made chemicals has increased exponentially recently, and exposure to some of them can induce fetal malformations. Because complex and precisely programmed signaling pathways play important roles in developmental processes, their disruption by external chemicals often triggers developmental toxicity. However, highly accurate and high-throughput screening assays for potential developmental toxicants are currently lacking. In this study, we propose a reporter assay that utilizes human-induced pluripotent stem cells (iPSCs) to detect changes in fibroblast growth factor signaling, which is essential for limb morphogenesis. The dynamics of this signaling after exposure to a chemical were integrated to estimate the degree of signaling disruption, which afforded a good prediction of the capacity of chemicals listed in the ECVAM International Validation Study that induce limb malformations. This study presents an initial report of a human iPSC-based signaling disruption assay, which could be useful for the screening of potential developmental toxicants.Graphical abstractDisplay OmittedHighlights•Human iPSC-based FGF signal disruption reporter system was established•FGF signal disruption was a good indicator of limb malformation-related toxicants•Integration of dynamic FGF signal disruption results improved assay performancePharmacological parameters Toxicology evaluation; Toxicity assessment; Embryology
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