4.8 Article

The biliary epithelium presents antigens to and activates natural killer T cells

期刊

HEPATOLOGY
卷 62, 期 4, 页码 1249-1259

出版社

WILEY
DOI: 10.1002/hep.27840

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资金

  1. South Eastern Norway Regional Health Authority [2012024]
  2. PSC
  3. Norwegian PSC Research Center
  4. Kristian Gerhard Jebsen Foundation
  5. National Institutes of Health [CA170194]
  6. Manchester Collaborative Centre for Inflammation Research
  7. Novo Nordisk Fonden [NNF14OC0009347] Funding Source: researchfish

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Cholangiocytes express antigen-presenting molecules, but it has been unclear whether they can present antigens. Natural killer T (NKT) cells respond to lipid antigens presented by the major histocompatibility complex class I-like molecule CD1d and are abundant in the liver. We investigated whether cholangiocytes express CD1d and present lipid antigens to NKT cells and how CD1d expression varies in healthy and diseased bile ducts. Murine and human cholangiocyte cell lines as well as human primary cholangiocytes expressed CD1d as determined by flow cytometry and western blotting. Murine cholangiocyte cell lines were able to present both exogenous and endogenous lipid antigens to invariant and noninvariant NKT cell hybridomas and primary NKT cells in a CD1d-dependent manner. A human cholangiocyte cell line, cholangiocarcinoma cell lines, and human primary cholangiocytes also presented exogenous CD1d-restricted antigens to invariant NKT cell clones. CD1d expression was down-regulated in the biliary epithelium of patients with late primary sclerosing cholangitis, primary biliary cirrhosis, and alcoholic cirrhosis compared to healthy controls. Conclusions: Cholangiocytes express CD1d and present antigens to NKT cells and CD1d expression is down-regulated in diseased biliary epithelium, findings which show that the biliary epithelium can activate an important lymphocyte subset of the liver. This is a potentially important immune pathway in the biliary system, which may be capable of regulating inflammation in the context of biliary disease. (Hepatology 2015;62:1249-1259)

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