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A multi-trap microfluidic chip enabling longitudinal studies of nerve regeneration in Caenorhabditis elegans.
Gokce, Sertan Kutal; Hegarty, Evan Marley; Mondal, Sudip; Zhao, Peisen; Ghorashian, Navid; Hilliard, Massimo A; Ben-Yakar, Adela.
Afiliación
  • Gokce SK; Electrical and Computer Engineering, The University of Texas at Austin, Austin, TX, 78712, USA.
  • Hegarty EM; Mechanical Engineering, The University of Texas at Austin, Austin, TX, 78712, USA.
  • Mondal S; Mechanical Engineering, The University of Texas at Austin, Austin, TX, 78712, USA.
  • Zhao P; Electrical and Computer Engineering, The University of Texas at Austin, Austin, TX, 78712, USA.
  • Ghorashian N; Biomedical Engineering, The University of Texas at Austin, Austin, TX, 78712, USA.
  • Hilliard MA; Queensland Brain Institute, The University of Queensland, Brisbane, QLD 4072, Australia.
  • Ben-Yakar A; Electrical and Computer Engineering, The University of Texas at Austin, Austin, TX, 78712, USA. ben-yakar@mail.utexas.edu.
Sci Rep ; 7(1): 9837, 2017 08 29.
Article en En | MEDLINE | ID: mdl-28852096
Several sophisticated microfluidic devices have recently been proposed for femtosecond laser axotomy in the nematode C. elegans for immobilization of the animals for surgery to overcome time-consuming and labor-intensive manual processes. However, nerve regeneration studies require long-term recovery of the animals and multiple imaging sessions to observe the regeneration capabilities of their axons post-injury. Here we present a simple, multi-trap device, consisting of a single PDMS (polydimethylsiloxane) layer, which can immobilize up to 20 animals at the favorable orientation for optical access needed for precise laser surgery and high-resolution imaging. The new device, named "worm hospital" allows us to perform the entire nerve regeneration studies, including on-chip axotomy, post-surgery housing for recovery, and post-recovery imaging all on one microfluidic chip. Utilizing the worm hospital and analysis of mutants, we observed that most but not all neurodevelopmental genes in the Wnt/Frizzled pathway are important for regeneration of the two touch receptor neurons ALM and PLM. Using our new chip, we observed that the cwn-2 and cfz-2 mutations significantly reduced the reconnection possibilities of both neurons without any significant reduction in the regrowth lengths of the severed axons. We observed a similar regeneration phenotype with cwn-1 mutation in ALM neurons only.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Caenorhabditis elegans / Microfluídica / Técnicas Analíticas Microfluídicas / Regeneración Nerviosa Tipo de estudio: Observational_studies Límite: Animals Idioma: En Revista: Sci Rep Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Caenorhabditis elegans / Microfluídica / Técnicas Analíticas Microfluídicas / Regeneración Nerviosa Tipo de estudio: Observational_studies Límite: Animals Idioma: En Revista: Sci Rep Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos