Neonatal NK cells target the mouse duct epithelium via Nkg2d and drive tissue-specific injury in experimental biliary atresia

J Clin Invest. 2009 Aug;119(8):2281-90. doi: 10.1172/jci38879.


Biliary atresia is a neonatal obstructive cholangiopathy that progresses to end-stage liver disease. Although the etiology is unknown, a neonatal adaptive immune signature has been mechanistically linked to obstruction of the extrahepatic bile ducts. Here, we investigated the role of the innate immune response in the pathogenesis of biliary atresia. Analysis of livers of infants at diagnosis revealed that NK cells populate the vicinity of intrahepatic bile ducts and overexpress several genes involved in cytotoxicity. Using a model of rotavirus-induced biliary atresia in newborn mice, we found that activated NK cells also populated murine livers and were the most abundant cells in extrahepatic bile ducts at the time of obstruction. Rotavirus-primed hepatic NK cells lysed cholangiocytes in a contact- and Nkg2d-dependent fashion. Depletion of NK cells and blockade of Nkg2d each prevented injury of the duct epithelium after rotavirus infection, maintained continuity of duct lumen between the liver and duodenum, and enabled bile flow, despite the presence of virus in the tissue and the overexpression of proinflammatory cytokines. These findings identify NK cells as key initiators of cholangiocyte injury via Nkg2d and demonstrate that injury to the duct epithelium drives the phenotype of experimental biliary atresia.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Animals, Newborn
  • Bile Ducts, Extrahepatic / pathology*
  • Biliary Atresia / etiology*
  • Biliary Atresia / immunology
  • Biliary Atresia / pathology
  • CD8-Positive T-Lymphocytes / immunology
  • Cytotoxicity, Immunologic
  • Disease Models, Animal
  • Humans
  • Immunity, Innate
  • Infant
  • Killer Cells, Natural / immunology*
  • Liver / pathology
  • Lymphocyte Activation
  • Mice
  • Mice, Inbred BALB C
  • NK Cell Lectin-Like Receptor Subfamily K / physiology*
  • Organ Specificity
  • Rotavirus


  • Klrk1 protein, mouse
  • NK Cell Lectin-Like Receptor Subfamily K