4.8 Article

Thymic NF-κB-inducing kinase regulates CD4+ T cell-elicited liver injury and fibrosis in mice

期刊

JOURNAL OF HEPATOLOGY
卷 67, 期 1, 页码 100-109

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jhep.2017.02.025

关键词

Liver injury; Inflammation; Liver fibrosis; CD4-positive T-lymphocytes; Hepatitis, autoimmune; Liver disease; Flow Cytometry; Liver cirrhosis

资金

  1. National Institutes of Health [DK091591, DK094014, AI121156]
  2. National Natural Science Foundation of China [81420108006]
  3. Michigan Diabetes Research and Training Center [NIH DK20572]
  4. University of Michigan's Cancer Center [NIH CA46592]
  5. University of Michigan Nathan Shock Center [NIH P30AG013283]
  6. University of Michigan Gut Peptide Research Center [NIH DK34933]

向作者/读者索取更多资源

Background & Aims: The liver is an immunologically-privileged organ. Breakdown of liver immune privilege has been reported in chronic liver disease; however, the role of adaptive immunity in liver injury is poorly defined. Nuclear factor-kappa B-inducing kinase (NIK) is known to regulate immune tissue development, but its role in maintaining liver homeostasis remains unknown. This study aimed to assess the role of NIK, particularly thymic NIK, in regulating liver adaptive immunity. Methods: NIK was deleted systemically or conditionally using the Cre/loxp system. Cluster of differentiation [CD]4(+) or CD8(+) T cells were depleted using anti-CD4 or anti-CD8 antibody. Donor bone marrows or thymi were transferred into recipient mice. Immune cells were assessed by immunohistochemistry and flow cytometry. Results: Global, but not liver-specific or hematopoietic lineage cell-specific, deletion of NIK induced fatal liver injury, inflammation, and fibrosis. Likewise, adoptive transfer of NIK-null, but not wild-type, thymi into immune-deficient mice induced liver inflammation, injury, and fibrosis in recipients. Liver inflammation was characterized by a massive expansion of T cells, particularly the CD4(+) T cell subpopulation. Depletion of CD4(+), but not CD8(+), T cells fully protected against liver injury, inflammation, and fibrosis in NIK-null mice. NIK deficiency also resulted in inflammation in the lung, kidney, and pancreas, but to a lesser degree relative to the liver. Conclusions: Thymic NIK suppresses development of autoreactive T cells against liver antigens, and NIK deficiency in the thymus results in CD4(+) T cell-orchestrated autoimmune hepatitis and liver fibrosis. Thus, thymic NIK is essential for the maintenance of liver immune privilege and liver homeostasis. Lay summary: We found that global or thymus-specific ablation of the NIK gene results in fatal autoimmune liver disease in mice. NIK-deficient mice develop liver inflammation, injury, and fibrosis. Our findings indicate that thymic NIK is essential for the maintenance of liver integrity and homeostasis. (C) 2017 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.

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