Abstract

Osteoarthritis is the most common joint disease in the world with significant societal consequences, but lacks effective disease modifying interventions. The pathophysiology consists of a prominent inflammatory component that can be targeted to prevent cartilage degradation and structural defects. Intracellular metabolism has emerged as a culprit of the inflammatory response in chondrocytes, with both processes co-regulating each other. The role of glutamine metabolism in chondrocytes, especially in the context of inflammation, lacks a thorough understanding and is the focus of this work. We display that mouse chondrocytes utilize glutamine for energy production and anabolic processes. Furthermore, we show that glutamine deprivation itself causes metabolic reprogramming and decreases the inflammatory response of chondrocytes through inhibition of NF-κB activity. Finally, we display that glutamine deprivation promotes autophagy and that ammonia is an inhibitor of autophagy. Overall, we identify a relationship between glutamine metabolism and inflammatory signaling and display the need for increased study of chondrocyte metabolic systems.

Data availability

All data generated or analysed during this study are included in the manuscript and supporting file. Source data have been provided for all figures

Article and author information

Author details

  1. Manoj Arra

    Department of Orthopaedic Surgery, Washington University Medical Center, St Louis, United States
    Competing interests
    No competing interests declared.
  2. Gaurav Swarnkar

    Department of Orthopaedic Surgery, Washington University Medical Center, St Louis, United States
    Competing interests
    No competing interests declared.
  3. Naga Suresh Adapala

    Department of Orthopaedic Surgery, Washington University Medical Center, St Louis, United States
    Competing interests
    No competing interests declared.
  4. Syeda-Kanwal Batool Naqvi

    Department of Orthopaedic Surgery, Washington University Medical Center, St Louis, United States
    Competing interests
    No competing interests declared.
  5. Lei Cai

    Department of Orthopaedic Surgery, Washington University Medical Center, St Louis, United States
    Competing interests
    No competing interests declared.
  6. Muhammad Farooq Rai

    Department of Orthopaedic Surgery, Washington University Medical Center, St Louis, United States
    Competing interests
    No competing interests declared.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-4826-4331
  7. Srikanth Singamaneni

    Department of Mechanical Engineering and Material Sciences, Washington University Medical Center, St Louis, United States
    Competing interests
    No competing interests declared.
  8. Gabriel Mbalaviele

    Bone and Mineral Division, Washington University Medical Center, St Louis, United States
    Competing interests
    No competing interests declared.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-4660-0952
  9. Robert Brophy

    Department of Orthopaedic Surgery, Washington University Medical Center, Saint Louis, United States
    Competing interests
    No competing interests declared.
  10. Yousef Abu-Amer

    Department of Orthopaedic Surgery, Washington University Medical Center, St Louis, United States
    For correspondence
    abuamery@wustl.edu
    Competing interests
    Yousef Abu-Amer, Reviewing editor, eLife.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-5890-5086

Funding

National Institute of Arthritis and Musculoskeletal and Skin Diseases (AR072623)

  • Yousef Abu-Amer

National Institute of Arthritis and Musculoskeletal and Skin Diseases (AR074992)

  • Yousef Abu-Amer

Shriners Hospitals for Children (85160-STL-20)

  • Yousef Abu-Amer

National Institute of Arthritis and Musculoskeletal and Skin Diseases (AR076758)

  • Gabriel Mbalaviele

National Institutes of Health (AI161022)

  • Gabriel Mbalaviele

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Ethics

Animal experimentation: This study was performed in strict accordance with the recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. All of the animals were handled according to approved institutional animal care and use committee (IACUC) protocols (#21-0413) of Washington University. All surgery was performed under sodium pentobarbital anesthesia, and every effort was made to minimize suffering.

Copyright

© 2022, Arra et al.

This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited.

Metrics

  • 1,859
    views
  • 381
    downloads
  • 13
    citations

Views, downloads and citations are aggregated across all versions of this paper published by eLife.

Download links

A two-part list of links to download the article, or parts of the article, in various formats.

Downloads (link to download the article as PDF)

Open citations (links to open the citations from this article in various online reference manager services)

Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)

  1. Manoj Arra
  2. Gaurav Swarnkar
  3. Naga Suresh Adapala
  4. Syeda-Kanwal Batool Naqvi
  5. Lei Cai
  6. Muhammad Farooq Rai
  7. Srikanth Singamaneni
  8. Gabriel Mbalaviele
  9. Robert Brophy
  10. Yousef Abu-Amer
(2022)
Glutamine metabolism modulates chondrocyte inflammatory response
eLife 11:e80725.
https://doi.org/10.7554/eLife.80725

Share this article

https://doi.org/10.7554/eLife.80725

Further reading

    1. Genetics and Genomics
    2. Immunology and Inflammation
    Stephanie Guillet, Tomi Lazarov ... Frédéric Geissmann
    Research Article

    Systemic lupus erythematosus (SLE) is an autoimmune disease, the pathophysiology and genetic basis of which are incompletely understood. Using a forward genetic screen in multiplex families with SLE, we identified an association between SLE and compound heterozygous deleterious variants in the non-receptor tyrosine kinases (NRTKs) ACK1 and BRK. Experimental blockade of ACK1 or BRK increased circulating autoantibodies in vivo in mice and exacerbated glomerular IgG deposits in an SLE mouse model. Mechanistically, NRTKs regulate activation, migration, and proliferation of immune cells. We found that the patients’ ACK1 and BRK variants impair efferocytosis, the MERTK-mediated anti-inflammatory response to apoptotic cells, in human induced pluripotent stem cell (hiPSC)-derived macrophages, which may contribute to SLE pathogenesis. Overall, our data suggest that ACK1 and BRK deficiencies are associated with human SLE and impair efferocytosis in macrophages.

    1. Immunology and Inflammation
    Hong Yu, Hiroshi Nishio ... Drew Pardoll
    Research Article

    The adaptive T cell response is accompanied by continuous rewiring of the T cell’s electric and metabolic state. Ion channels and nutrient transporters integrate bioelectric and biochemical signals from the environment, setting cellular electric and metabolic states. Divergent electric and metabolic states contribute to T cell immunity or tolerance. Here, we report in mice that neuritin (Nrn1) contributes to tolerance development by modulating regulatory and effector T cell function. Nrn1 expression in regulatory T cells promotes its expansion and suppression function, while expression in the T effector cell dampens its inflammatory response. Nrn1 deficiency in mice causes dysregulation of ion channel and nutrient transporter expression in Treg and effector T cells, resulting in divergent metabolic outcomes and impacting autoimmune disease progression and recovery. These findings identify a novel immune function of the neurotrophic factor Nrn1 in regulating the T cell metabolic state in a cell context-dependent manner and modulating the outcome of an immune response.