Growth Hormone Stops Excessive Inflammation After Partial Hepatectomy, Allowing Liver Regeneration and Survival Through Induction of H2-Bl/HLA-G

Mayumi Ishikawa, Andrew J Brooks, Manuel A Fernández-Rojo, Johan Medina, Yash Chhabra, Shiro Minami, Kathryn A Tunny, Robert G Parton, Julian P Vivian, Jamie Rossjohn, Viral Chikani, Grant A Ramm, Ken K Y Ho, Michael J Waters

Research output: Contribution to journalArticlepeer-review

27 Scopus citations

Abstract

BACKGROUND AND AIMS: Growth hormone (GH) is important for liver regeneration after partial hepatectomy (PHx). We investigated this process in C57BL/6 mice that express different forms of the GH receptor (GHR) with deletions in key signaling domains.

APPROACH AND RESULTS: PHx was performed on C57BL/6 mice lacking GHR (Ghr-/- ), disabled for all GH-dependent Janus kinase 2 signaling (Box1-/- ), or lacking only GH-dependent signal transducer and activator of transcription 5 (STAT5) signaling (Ghr391-/- ), and wild-type littermates. C57BL/6 Ghr-/- mice showed striking mortality within 48 hours after PHx, whereas Box1-/- or Ghr391-/- mice survived with normal liver regeneration. Ghr-/- mortality was associated with increased apoptosis and elevated natural killer/natural killer T cell and macrophage cell markers. We identified H2-Bl, a key immunotolerance protein, which is up-regulated by PHx through a GH-mediated, Janus kinase 2-independent, SRC family kinase-dependent pathway. GH treatment was confirmed to up-regulate expression of the human homolog of H2-Bl (human leukocyte antigen G [HLA-G]) in primary human hepatocytes and in the serum of GH-deficient patients. We find that injury-associated innate immune attack by natural killer/natural killer T cell and macrophage cells are instrumental in the failure of liver regeneration, and this can be overcome in Ghr-/- mice by adenoviral delivery of H2-Bl or by infusion of HLA-G protein. Further, H2-Bl knockdown in wild-type C57BL/6 mice showed elevated markers of inflammation after PHx, whereas Ghr-/- backcrossed on a strain with high endogenous H2-Bl expression showed a high rate of survival following PHx.

CONCLUSIONS: GH induction of H2-Bl expression is crucial for reducing innate immune-mediated apoptosis and promoting survival after PHx in C57BL/6 mice. Treatment with HLA-G may lead to improved clinical outcomes following liver surgery or transplantation.

Original languageEnglish
Pages (from-to)759-775
Number of pages17
JournalHepatology
Volume73
Issue number2
DOIs
StatePublished - Feb 2021
Externally publishedYes

Keywords

  • Animals
  • Apoptosis/immunology
  • Carrier Proteins/genetics
  • Cells, Cultured
  • Coculture Techniques
  • Gene Knockdown Techniques
  • Growth Hormone/deficiency
  • H-2 Antigens/genetics
  • HLA-G Antigens/genetics
  • Hepatectomy
  • Hepatocytes
  • Humans
  • Immunity, Innate
  • Killer Cells, Natural/immunology
  • Liver/physiology
  • Liver Regeneration/immunology
  • Macrophages/immunology
  • Mice
  • Natural Killer T-Cells/immunology
  • Primary Cell Culture
  • Recombinant Proteins/genetics
  • Signal Transduction/genetics

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