Mincle signaling promotes con A hepatitis

Stephanie H. Greco, Alejandro Torres-Hernandez, Aleksandr Kalabin, Clint Whiteman, Rae Rokosh, Sushma Ravirala, Atsuo Ochi, Johana Gutierrez, Muhammad Atif Salyana, Vishnu R. Mani, Savitha V. Nagaraj, Michael Deutsch, Lena Seifert, Donnele Daley, Rocky Barilla, Mautin Hundeyin, Yuriy Nikifrov, Karla Tejada, Bruce E. Gelb, Steven C. KatzGeorge Miller

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15 Scopus citations

Abstract

Con A hepatitis is regarded as a T cell-mediated model of acute liver injury. Mincle is a C-Type lectin receptor that is critical in the immune response to mycobacteria and fungi but does not have a well-defined role in preclinical models of non-pathogen-mediated inflammation. Because Mincle can ligate the cell death ligand SAP130, we postulated that Mincle signaling drives intrahepatic inflammation and liver injury in Con A hepatitis. Acute liver injury was assessed in the murine Con A hepatitis model using C57BL/6, Mincle-/-, and Dectin-1-/- mice. The role of C/EBPb and hypoxia-inducible factor-1α (HIF-1α ) signaling was assessed using selective inhibitors. We found that Mincle was highly expressed in hepatic innate inflammatory cells and endothelial cells in both mice and humans. Furthermore, sterile Mincle ligands and Mincle signaling intermediates were increased in the murine liver in Con A hepatitis. Most significantly, Mincle deletion or blockade protected against Con A hepatitis, whereas Mincle ligation exacerbated disease. Bone marrow chimeric and adoptive transfer experiments suggested that Mincle signaling in infiltrating myeloid cells dictates disease phenotype. Conversely, signaling via other C-Type lectin receptors did not alter disease course. Mechanistically, we found that Mincle blockade decreased the NF-κβ-related signaling intermediates C/EBPb and HIF-1a, both of which are necessary in macrophage-mediated inflammatory responses. Accordingly, Mincle deletion lowered production of nitrites in Con A hepatitis and inhibition of both C/EBPb and HIF-1α reduced the severity of liver disease. Our work implicates a novel innate immune driver of Con A hepatitis and, more broadly, suggests a potential role for Mincle in diseases governed by sterile inflammation. The Journal of Immunology, 2016, 197: 2816-2827.

Original languageEnglish (US)
Pages (from-to)2816-2827
Number of pages12
JournalJournal of Immunology
Volume197
Issue number7
DOIs
StatePublished - Oct 1 2016

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All Science Journal Classification (ASJC) codes

  • Immunology and Allergy
  • Immunology

Cite this

Greco, S. H., Torres-Hernandez, A., Kalabin, A., Whiteman, C., Rokosh, R., Ravirala, S., Ochi, A., Gutierrez, J., Salyana, M. A., Mani, V. R., Nagaraj, S. V., Deutsch, M., Seifert, L., Daley, D., Barilla, R., Hundeyin, M., Nikifrov, Y., Tejada, K., Gelb, B. E., ... Miller, G. (2016). Mincle signaling promotes con A hepatitis. Journal of Immunology, 197(7), 2816-2827. https://doi.org/10.4049/jimmunol.1600598