| Literature DB >> 33354870 |
Ellen Fritsche1,2, Thomas Haarmann-Stemmann1, Julia Kapr1, Saskia Galanjuk1, Julia Hartmann1, Peter R Mertens3, Angela A M Kämpfer1, Roel P F Schins1, Julia Tigges1, Katharina Koch1.
Abstract
The call for a paradigm change in toxicology from the United States National Research Council in 2007 initiates awareness for the invention and use of human-relevant alternative methods for toxicological hazard assessment. Simple 2D in vitro systems may serve as first screening tools, however, recent developments infer the need for more complex, multicellular organotypic models, which are superior in mimicking the complexity of human organs. In this review article most critical organs for toxicity assessment, i.e., skin, brain, thyroid system, lung, heart, liver, kidney, and intestine are discussed with regards to their functions in health and disease. Embracing the manifold modes-of-action how xenobiotic compounds can interfere with physiological organ functions and cause toxicity, the need for translation of such multifaceted organ features into the dish seems obvious. Currently used in vitro methods for toxicological applications and ongoing developments not yet arrived in toxicity testing are discussed, especially highlighting the potential of models based on embryonic stem cells and induced pluripotent stem cells of human origin. Finally, the application of innovative technologies like organs-on-a-chip and genome editing point toward a toxicological paradigm change moves into action.Entities:
Keywords: 3R; alternative methods; high throughput; human-induced pluripotent stem cells; organoids; risk assessment
Mesh:
Year: 2020 PMID: 33354870 DOI: 10.1002/smll.202006252
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281