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Structuring a multi-nodal neural network in vitro within a novel design microfluidic chip.
van de Wijdeven, Rosanne; Ramstad, Ola Huse; Bauer, Ulrich Stefan; Halaas, Øyvind; Sandvig, Axel; Sandvig, Ioanna.
Afiliación
  • van de Wijdeven R; Department of Clinical and Molecular Medicine, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, PO Box 8905 MTFS, NO-7491, Trondheim, Norway. Rosanne.v.d.wijdeven@ntnu.no.
  • Ramstad OH; Department of Neuromedicine and Movement Science, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, N-7491, Trondheim, Norway.
  • Bauer US; Department of Neuromedicine and Movement Science, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, N-7491, Trondheim, Norway.
  • Halaas Ø; Department of Clinical and Molecular Medicine, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, PO Box 8905 MTFS, NO-7491, Trondheim, Norway.
  • Sandvig A; Department of Neuromedicine and Movement Science, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, N-7491, Trondheim, Norway.
  • Sandvig I; Department of Pharmacology and Clinical Neurosciences, Division of Neuro, Head and Neck, Umeå University Hospital, SE-90187, Umeå, Sweden.
Biomed Microdevices ; 20(1): 9, 2018 01 02.
Article en En | MEDLINE | ID: mdl-29294210
ABSTRACT
Neural network formation is a complex process involving axon outgrowth and guidance. Axon guidance is facilitated by structural and molecular cues from the surrounding microenvironment. Micro-fabrication techniques can be employed to produce microfluidic chips with a highly controlled microenvironment for neural cells enabling longitudinal studies of complex processes associated with network formation. In this work, we demonstrate a novel open microfluidic chip design that encompasses a freely variable number of nodes interconnected by axon-permissible tunnels, enabling structuring of multi-nodal neural networks in vitro. The chip employs a partially open design to allow high level of control and reproducibility of cell seeding, while reducing shear stress on the cells. We show that by culturing dorsal root ganglion cells (DRGs) in our microfluidic chip, we were able to structure a neural network in vitro. These neurons were compartmentalized within six nodes interconnected through axon growth tunnels. Furthermore, we demonstrate the additional benefit of open top design by establishing a 3D neural culture in matrigel and a neuronal aggregate 3D culture within the chips. In conclusion, our results demonstrate a novel microfluidic chip design applicable to structuring complex neural networks in vitro, thus providing a versatile, highly relevant platform for the study of neural network dynamics applicable to developmental and regenerative neuroscience.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Técnicas de Cultivo de Célula / Dispositivos Laboratorio en un Chip / Red Nerviosa Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Animals Idioma: En Revista: Biomed Microdevices Asunto de la revista: ENGENHARIA BIOMEDICA Año: 2018 Tipo del documento: Article País de afiliación: Noruega

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Técnicas de Cultivo de Célula / Dispositivos Laboratorio en un Chip / Red Nerviosa Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Animals Idioma: En Revista: Biomed Microdevices Asunto de la revista: ENGENHARIA BIOMEDICA Año: 2018 Tipo del documento: Article País de afiliación: Noruega