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Molecular profiling of enteric nervous system cell lineages.
Obata, Yuuki; Castaño, Álvaro; Fallesen, Todd L; Bon-Frauches, Ana Carina; Boeing, Stefan; Huseynova, Almaz; McCallum, Sarah; Lasrado, Reena; Heanue, Tiffany A; Pachnis, Vassilis.
Afiliação
  • Obata Y; Development and Homeostasis of the Nervous System Laboratory, The Francis Crick Institute, London, UK. Yuki.Obata@UTsouthwestern.edu.
  • Castaño Á; Department of Immunology, Department of Neuroscience, University of Texas Southwestern Medical Center, Dallas, TX, USA. Yuki.Obata@UTsouthwestern.edu.
  • Fallesen TL; Development and Homeostasis of the Nervous System Laboratory, The Francis Crick Institute, London, UK.
  • Bon-Frauches AC; MRC London Institute of Medical Sciences, Imperial College London, London, UK.
  • Boeing S; Crick Advanced Light Microscopy, The Francis Crick Institute, London, UK.
  • Huseynova A; Development and Homeostasis of the Nervous System Laboratory, The Francis Crick Institute, London, UK.
  • McCallum S; Bionformatics & Biostatistics, The Francis Crick Institute, London, UK.
  • Lasrado R; Software Development & Machine Learning Team, The Francis Crick Institute, London, UK.
  • Heanue TA; Kinases and Brain Development Laboratory, The Francis Crick Institute, London, UK.
  • Pachnis V; Development and Homeostasis of the Nervous System Laboratory, The Francis Crick Institute, London, UK.
Nat Protoc ; 17(8): 1789-1817, 2022 08.
Article em En | MEDLINE | ID: mdl-35676375
ABSTRACT
The enteric nervous system (ENS) is an extensive network of enteric neurons and glial cells that is intrinsic to the gut wall and regulates almost all aspects of intestinal physiology. While considerable advancement has been made in understanding the genetic programs regulating ENS development, there is limited understanding of the molecular pathways that control ENS function in adult stages. One of the limitations in advancing the molecular characterization of the adult ENS relates to technical difficulties in purifying healthy neurons and glia from adult intestinal tissues. To overcome this, we developed novel methods for performing transcriptomic analysis of enteric neurons and glia, which are based on the isolation of fluorescently labeled nuclei. Here we provide a step-by-step protocol for the labeling of adult mouse enteric neuronal nuclei using adeno-associated-virus-mediated gene transfer, isolation of the labeled nuclei by fluorimetric analysis, RNA purification and nuclear RNA sequencing. This protocol has also been adapted for the isolation of enteric neuron and glia nuclei from myenteric plexus preparations from adult zebrafish intestine. Finally, we describe a method for visualization and quantification of RNA in myenteric ganglia Spatial Integration of Granular Nuclear Signals (SIGNS). By following this protocol, it takes ~3 d to generate RNA and create cDNA libraries for nuclear RNA sequencing and 4 d to carry out high-resolution RNA expression analysis on ENS tissues.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peixe-Zebra / Sistema Nervoso Entérico Limite: Animals Idioma: En Revista: Nat Protoc Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peixe-Zebra / Sistema Nervoso Entérico Limite: Animals Idioma: En Revista: Nat Protoc Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido