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Regional Differences in Human Biliary Tissues and Corresponding In Vitro-Derived Organoids.
Rimland, Casey A; Tilson, Samantha G; Morell, Carola M; Tomaz, Rute A; Lu, Wei-Yu; Adams, Simone E; Georgakopoulos, Nikitas; Otaizo-Carrasquero, Francisco; Myers, Timothy G; Ferdinand, John R; Gieseck, Richard L; Sampaziotis, Fotios; Tysoe, Olivia C; Ross, Alexander; Kraiczy, Judith M; Wesley, Brandon; Muraro, Daniele; Zilbauer, Matthias; Oniscu, Gabriel C; Hannan, Nicholas R F; Forbes, Stuart J; Saeb-Parsy, Kourosh; Wynn, Thomas A; Vallier, Ludovic.
Afiliação
  • Rimland CA; Wellcome-Medical Research Council Cambridge Stem Cell Institute, University of Cambridge, Cambridge, United Kingdom.
  • Tilson SG; Immunopathogenesis Section, Laboratory of Parasitic Diseases, NIAID, NIH, Bethesda, MD.
  • Morell CM; Department of Surgery, University of Cambridge and National Institute for Health Research Cambridge Biomedical Research Centre, Cambridge, United Kingdom.
  • Tomaz RA; Medical Scientist Training Program, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC.
  • Lu WY; Wellcome-Medical Research Council Cambridge Stem Cell Institute, University of Cambridge, Cambridge, United Kingdom.
  • Adams SE; Department of Surgery, University of Cambridge and National Institute for Health Research Cambridge Biomedical Research Centre, Cambridge, United Kingdom.
  • Georgakopoulos N; Welcome Trust Sanger Institute, Hinxton, United Kingdom.
  • Otaizo-Carrasquero F; Liver Diseases Branch, NIDDK, NIH, Bethesda, MD.
  • Myers TG; Wellcome-Medical Research Council Cambridge Stem Cell Institute, University of Cambridge, Cambridge, United Kingdom.
  • Ferdinand JR; Department of Surgery, University of Cambridge and National Institute for Health Research Cambridge Biomedical Research Centre, Cambridge, United Kingdom.
  • Gieseck RL; Wellcome-Medical Research Council Cambridge Stem Cell Institute, University of Cambridge, Cambridge, United Kingdom.
  • Sampaziotis F; Department of Surgery, University of Cambridge and National Institute for Health Research Cambridge Biomedical Research Centre, Cambridge, United Kingdom.
  • Tysoe OC; MRC Centre for Regenerative Medicine, University of Edinburgh, Edinburgh, United Kingdom.
  • Ross A; Centre for Liver and Gastrointestinal Research, Institute of Immunology and Immunotherapy, The University of Birmingham, Birmingham, United Kingdom.
  • Kraiczy JM; Wellcome-Medical Research Council Cambridge Stem Cell Institute, University of Cambridge, Cambridge, United Kingdom.
  • Wesley B; Immunopathogenesis Section, Laboratory of Parasitic Diseases, NIAID, NIH, Bethesda, MD.
  • Muraro D; Department of Biological Sciences, North Carolina State University, Raleigh, NC.
  • Zilbauer M; Department of Surgery, University of Cambridge and National Institute for Health Research Cambridge Biomedical Research Centre, Cambridge, United Kingdom.
  • Oniscu GC; Genomic Technologies Section, Research Technologies Branch, NIAID, NIH, Bethesda, MD.
  • Hannan NRF; Genomic Technologies Section, Research Technologies Branch, NIAID, NIH, Bethesda, MD.
  • Forbes SJ; Department of Medicine, University of Cambridge, Cambridge, United Kingdom.
  • Saeb-Parsy K; Immunopathogenesis Section, Laboratory of Parasitic Diseases, NIAID, NIH, Bethesda, MD.
  • Wynn TA; Wellcome-Medical Research Council Cambridge Stem Cell Institute, University of Cambridge, Cambridge, United Kingdom.
  • Vallier L; Department of Surgery, University of Cambridge and National Institute for Health Research Cambridge Biomedical Research Centre, Cambridge, United Kingdom.
Hepatology ; 73(1): 247-267, 2021 01.
Article em En | MEDLINE | ID: mdl-32222998
ABSTRACT
BACKGROUND AND

AIMS:

Organoids provide a powerful system to study epithelia in vitro. Recently, this approach was applied successfully to the biliary tree, a series of ductular tissues responsible for the drainage of bile and pancreatic secretions. More precisely, organoids have been derived from ductal tissue located outside (extrahepatic bile ducts; EHBDs) or inside the liver (intrahepatic bile ducts; IHBDs). These organoids share many characteristics, including expression of cholangiocyte markers such as keratin (KRT) 19. However, the relationship between these organoids and their tissues of origin, and to each other, is largely unknown. APPROACH AND

RESULTS:

Organoids were derived from human gallbladder, common bile duct, pancreatic duct, and IHBDs using culture conditions promoting WNT signaling. The resulting IHBD and EHBD organoids expressed stem/progenitor markers leucine-rich repeat-containing G-protein-coupled receptor 5/prominin 1 and ductal markers KRT19/KRT7. However, RNA sequencing revealed that organoids conserve only a limited number of regional-specific markers corresponding to their location of origin. Of particular interest, down-regulation of biliary markers and up-regulation of cell-cycle genes were observed in organoids. IHBD and EHBD organoids diverged in their response to WNT signaling, and only IHBDs were able to express a low level of hepatocyte markers under differentiation conditions.

CONCLUSIONS:

Taken together, our results demonstrate that differences exist not only between extrahepatic biliary organoids and their tissue of origin, but also between IHBD and EHBD organoids. This information may help to understand the tissue specificity of cholangiopathies and also to identify targets for therapeutic development.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ductos Biliares Intra-Hepáticos / Organoides / Ductos Biliares Extra-Hepáticos / Células Epiteliais Idioma: En Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ductos Biliares Intra-Hepáticos / Organoides / Ductos Biliares Extra-Hepáticos / Células Epiteliais Idioma: En Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Reino Unido