| Literature DB >> 35393121 |
Christopher D Kassotis1, Frederick S Vom Saal2, Patrick J Babin3, Dominique Lagadic-Gossmann4, Helene Le Mentec4, Bruce Blumberg5, Nicole Mohajer5, Antoine Legrand4, Vesna Munic Kos6, Corinne Martin-Chouly4, Normand Podechard4, Sophie Langouët4, Charbel Touma4, Robert Barouki7, Min Ji Kim8, Karine Audouze9, Mahua Choudhury10, Nitya Shree10, Amita Bansal11, Sarah Howard12, Jerrold J Heindel12.
Abstract
There is increasing evidence of a role for environmental contaminants in disrupting metabolic health in both humans and animals. Despite a growing need for well-understood models for evaluating adipogenic and potential obesogenic contaminants, there has been a reliance on decades-old in vitro models that have not been appropriately managed by cell line providers. There has been a quick rise in available in vitro models in the last ten years, including commercial availability of human mesenchymal stem cell and preadipocyte models; these models require more comprehensive validation but demonstrate real promise in improved translation to human metabolic health. There is also progress in developing three-dimensional and co-culture techniques that allow for the interrogation of a more physiologically relevant state. While diverse rodent models exist for evaluating putative obesogenic and/or adipogenic chemicals in a physiologically relevant context, increasing capabilities have been identified for alternative model organisms such as Drosophila, C. elegans, zebrafish, and medaka in metabolic health testing. These models have several appreciable advantages, including most notably their size, rapid development, large brood sizes, and ease of high-resolution lipid accumulation imaging throughout the organisms. They are anticipated to expand the capabilities of metabolic health research, particularly when coupled with emerging obesogen evaluation techniques as described herein.Entities:
Keywords: 3T3-L1; Adipogenesis; Mesenchymal stem cells; Obesity; Zebrafish
Mesh:
Year: 2022 PMID: 35393121 PMCID: PMC9050906 DOI: 10.1016/j.bcp.2022.115014
Source DB: PubMed Journal: Biochem Pharmacol ISSN: 0006-2952 Impact factor: 6.100