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Modular automated microfluidic cell culture platform reduces glycolytic stress in cerebral cortex organoids

Organ-on-a-chip systems combine microfluidics, cell biology, and tissue engineering to culture 3D organ-specific in vitro models that recapitulate the biology and physiology of their in vivo counterparts. Here, we have developed a multiplex platform that automates the culture of individual organoids...

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Detalles Bibliográficos
Autores principales: Seiler, Spencer T., Mantalas, Gary L., Selberg, John, Cordero, Sergio, Torres-Montoya, Sebastian, Baudin, Pierre V., Ly, Victoria T., Amend, Finn, Tran, Liam, Hoffman, Ryan N., Rolandi, Marco, Green, Richard E., Haussler, David, Salama, Sofie R., Teodorescu, Mircea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9684529/
https://www.ncbi.nlm.nih.gov/pubmed/36418910
http://dx.doi.org/10.1038/s41598-022-20096-9
Descripción
Sumario:Organ-on-a-chip systems combine microfluidics, cell biology, and tissue engineering to culture 3D organ-specific in vitro models that recapitulate the biology and physiology of their in vivo counterparts. Here, we have developed a multiplex platform that automates the culture of individual organoids in isolated microenvironments at user-defined media flow rates. Programmable workflows allow the use of multiple reagent reservoirs that may be applied to direct differentiation, study temporal variables, and grow cultures long term. Novel techniques in polydimethylsiloxane (PDMS) chip fabrication are described here that enable features on the upper and lower planes of a single PDMS substrate. RNA sequencing (RNA-seq) analysis of automated cerebral cortex organoid cultures shows benefits in reducing glycolytic and endoplasmic reticulum stress compared to conventional in vitro cell cultures.