Growth hormone stops excessive inflammation after partial hepatectomy, allowing liver regeneration and survival through induction of H2-Bl/HLA-G

Journal article


Ishikawa, Mayumi, Brooks, Andrew J., Fernández-Rojo, Manuel A., Medina, Johan, Chhabra, Yash, Minami, Shiro, Tunny, Kathryn A., Parton, Robert G., Vivian, Julian Philip, Rossjohn, Jamie, Chikani, Viral, Ramm, Grant A., Ho, Ken K.Y. and Waters, Michael J.. (2021). Growth hormone stops excessive inflammation after partial hepatectomy, allowing liver regeneration and survival through induction of H2-Bl/HLA-G. Hepatology. 73(2), pp. 759-775. https://doi.org/10.1002/hep.31297
AuthorsIshikawa, Mayumi, Brooks, Andrew J., Fernández-Rojo, Manuel A., Medina, Johan, Chhabra, Yash, Minami, Shiro, Tunny, Kathryn A., Parton, Robert G., Vivian, Julian Philip, Rossjohn, Jamie, Chikani, Viral, Ramm, Grant A., Ho, Ken K.Y. and Waters, Michael J.
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.

Year2021
JournalHepatology
Journal citation73 (2), pp. 759-775
PublisherWolters Kluwer
ISSN0270-9139
Digital Object Identifier (DOI)https://doi.org/10.1002/hep.31297
PubMed ID32342533
Scopus EID2-s2.0-85091472471
PubMed Central IDPMC7894545
Open accessPublished as ‘gold’ (paid) open access
Page range759-775
FunderNational Health and Medical Research Council (NHMRC)
Australian Research Council (ARC)
Spanish Government
Diabetes Australia
TALENTO
Publisher's version
License
File Access Level
Open
Output statusPublished
Publication dates
OnlineFeb 2021
Publication process dates
Accepted07 Apr 2020
Deposited28 Nov 2023
ARC Funded ResearchThis output has been funded, wholly or partially, under the Australian Research Council Act 2001
Grant ID1124026
1025094
1025082
APP1156489
T1-BIO-1854
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https://acuresearchbank.acu.edu.au/item/8zzqx/growth-hormone-stops-excessive-inflammation-after-partial-hepatectomy-allowing-liver-regeneration-and-survival-through-induction-of-h2-bl-hla-g

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