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Multi-Organ toxicity demonstration in a functional human in vitro system composed of four organs

We report on a functional human model to evaluate multi-organ toxicity in a 4-organ system under continuous flow conditions in a serum-free defined medium utilizing a pumpless platform for 14 days. Computer simulations of the platform established flow rates and resultant shear stress within accepted...

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Detalles Bibliográficos
Autores principales: Oleaga, Carlota, Bernabini, Catia, Smith, Alec S.T., Srinivasan, Balaji, Jackson, Max, McLamb, William, Platt, Vivien, Bridges, Richard, Cai, Yunqing, Santhanam, Navaneetha, Berry, Bonnie, Najjar, Sarah, Akanda, Nesar, Guo, Xiufang, Martin, Candace, Ekman, Gail, Esch, Mandy B., Langer, Jessica, Ouedraogo, Gladys, Cotovio, Jose, Breton, Lionel, Shuler, Michael L., Hickman, James J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4738272/
https://www.ncbi.nlm.nih.gov/pubmed/26837601
http://dx.doi.org/10.1038/srep20030
Descripción
Sumario:We report on a functional human model to evaluate multi-organ toxicity in a 4-organ system under continuous flow conditions in a serum-free defined medium utilizing a pumpless platform for 14 days. Computer simulations of the platform established flow rates and resultant shear stress within accepted ranges. Viability of the system was demonstrated for 14 days as well as functional activity of cardiac, muscle, neuronal and liver modules. The pharmacological relevance of the integrated modules were evaluated for their response at 7 days to 5 drugs with known side effects after a 48 hour drug treatment regime. The results of all drug treatments were in general agreement with published toxicity results from human and animal data. The presented phenotypic culture model exhibits a multi-organ toxicity response, representing the next generation of in vitro systems, and constitutes a step towards an in vitro “human-on-a-chip” assay for systemic toxicity screening.