4.8 Review

Stem Cells for Next Level Toxicity Testing in the 21st Century

期刊

SMALL
卷 17, 期 15, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202006252

关键词

3R; alternative methods; high throughput; human‐ induced pluripotent stem cells; organoids; risk assessment

资金

  1. project CERST (Center for Alternatives to Animal Testing) of the Ministry for culture and science of the State of North-Rhine Westphalia, Germany [233-1.08.03.03-121972/131-1.08.03.03-121972]
  2. European Union's Horizon 2020 Research and Innovation Program of the ENDpoiNTs project [825759]
  3. German Research Foundation [97850925, SFB 854, GRK 2408, ME-1365/7-2, ME-1365/9-2]
  4. Projekt DEAL

向作者/读者索取更多资源

The call for a paradigm change in toxicology initiated by the United States National Research Council in 2007 highlights the importance of human-relevant alternative methods for toxicological hazard assessment. This review article discusses critical organs such as skin, brain, and lungs in terms of their functions in health and disease, emphasizing the need for more complex organotypic models. Innovative technologies like organs-on-a-chip and genome editing are paving the way for a shift in toxicological paradigm towards more advanced and human-specific approaches.
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.

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