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TALPID3/KIAA0586 Regulates Multiple Aspects of Neuromuscular Patterning During Gastrointestinal Development in Animal Models and Human.
Delalande, Jean Marie; Nagy, Nandor; McCann, Conor J; Natarajan, Dipa; Cooper, Julie E; Carreno, Gabriela; Dora, David; Campbell, Alison; Laurent, Nicole; Kemos, Polychronis; Thomas, Sophie; Alby, Caroline; Attié-Bitach, Tania; Lyonnet, Stanislas; Logan, Malcolm P; Goldstein, Allan M; Davey, Megan G; Hofstra, Robert M W; Thapar, Nikhil; Burns, Alan J.
Afiliação
  • Delalande JM; Centre for Immunobiology, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.
  • Nagy N; Stem Cells and Regenerative Medicine, Birth Defects Research Centre, UCL Great Ormond Street Institute of Child Health, London, United Kingdom.
  • McCann CJ; Department of Anatomy, Histology and Embryology, Semmelweis University, Budapest, Hungary.
  • Natarajan D; Stem Cells and Regenerative Medicine, Birth Defects Research Centre, UCL Great Ormond Street Institute of Child Health, London, United Kingdom.
  • Cooper JE; Stem Cells and Regenerative Medicine, Birth Defects Research Centre, UCL Great Ormond Street Institute of Child Health, London, United Kingdom.
  • Carreno G; Developmental Biology and Cancer Program, Birth Defects Research Centre, UCL Great Ormond Street Institute of Child Health, London, United Kingdom.
  • Dora D; Developmental Biology and Cancer Program, Birth Defects Research Centre, UCL Great Ormond Street Institute of Child Health, London, United Kingdom.
  • Campbell A; Department of Anatomy, Histology and Embryology, Semmelweis University, Budapest, Hungary.
  • Laurent N; Department of Paediatric Surgery, Christchurch Hospital, Christchurch, New Zealand.
  • Kemos P; Génétique et Anomalies du Développement, Université de Bourgogne, Service d'Anatomie Pathologique, Dijon, France.
  • Thomas S; Centre for Immunobiology, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.
  • Alby C; Laboratory of Embryology and Genetics of Congenital Malformations, INSERM UMR 1163 Institut Imagine, Paris, France.
  • Attié-Bitach T; Department of Genetics, Hôpital Necker-Enfants Malades, Assistance Publique Hôpitaux de Paris (AP-HP), Paris, France.
  • Lyonnet S; Laboratory of Embryology and Genetics of Congenital Malformations, INSERM UMR 1163 Institut Imagine, Paris, France.
  • Logan MP; Department of Genetics, Hôpital Necker-Enfants Malades, Assistance Publique Hôpitaux de Paris (AP-HP), Paris, France.
  • Goldstein AM; Paris Descartes, Sorbonne Paris Cité, Paris, France.
  • Davey MG; Laboratory of Embryology and Genetics of Congenital Malformations, INSERM UMR 1163 Institut Imagine, Paris, France.
  • Hofstra RMW; Department of Genetics, Hôpital Necker-Enfants Malades, Assistance Publique Hôpitaux de Paris (AP-HP), Paris, France.
  • Thapar N; Paris Descartes, Sorbonne Paris Cité, Paris, France.
  • Burns AJ; Randall Division of Cell and Molecular Biophysics, King's College London, London, United Kingdom.
Front Mol Neurosci ; 14: 757646, 2021.
Article em En | MEDLINE | ID: mdl-35002618
TALPID3/KIAA0586 is an evolutionary conserved protein, which plays an essential role in protein trafficking. Its role during gastrointestinal (GI) and enteric nervous system (ENS) development has not been studied previously. Here, we analyzed chicken, mouse and human embryonic GI tissues with TALPID3 mutations. The GI tract of TALPID3 chicken embryos was shortened and malformed. Histologically, the gut smooth muscle was mispatterned and enteric neural crest cells were scattered throughout the gut wall. Analysis of the Hedgehog pathway and gut extracellular matrix provided causative reasons for these defects. Interestingly, chicken intra-species grafting experiments and a conditional knockout mouse model showed that ENS formation did not require TALPID3, but was dependent on correct environmental cues. Surprisingly, the lack of TALPID3 in enteric neural crest cells (ENCC) affected smooth muscle and epithelial development in a non-cell-autonomous manner. Analysis of human gut fetal tissues with a KIAA0586 mutation showed strikingly similar findings compared to the animal models demonstrating conservation of TALPID3 and its necessary role in human GI tract development and patterning.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Front Mol Neurosci Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Front Mol Neurosci Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Reino Unido