TRIM21 facilitates inflammasome assembly and contributes to autoinflammatory disease

Inflammasomes are cytosolic multiprotein complexes facilitating the maturation and release of the inflammatory cytokines interleukin (IL)-1β and IL-18 and pyroptosis. ASC (apoptosis-associated-speck-like protein containing a CARD) is the central inflammasome adaptor. ASC polymerization is crucial for inflammasome assembly, and ASC particle release propagates inflammasome responses to bystander cells. However, control of inflammasome and ASC particle assembly to limit chronic inflammation and the emergence of autoinflammatory diseases is still incompletely understood. Here, we show that the E3 ubiquitin ligase TRIM (tripartite-motif-containing protein) 21, a common autoantigen in autoimmune diseases, is involved in inflammasome assembly. Specifically, TRIM21 binds to and ubiquitinates ASC to facilitate ASC/NLRP3 interactions, ASC polymerization and the release of ASC/TRIM21-containing particles during pyroptosis in human and mouse macrophages. Furthermore, we detect systemic ASC/TRIM21 particles and autoantibodies in human and mouse autoinflammatory disease. Thus, our findings highlight a previously unrecognized role of TRIM21 as an inflammasome component and driver of autoinflammation.

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Publication Details

Journal
Nature Communications
Published
2026-05-22
DOI
https://doi.org/10.1038/s41467-026-73350-3
Primary Topic
Inflammasome and immune disorders
Type
article
Field-Weighted Citation Impact
0.00

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article

TRIM21 facilitates inflammasome assembly and contributes to autoinflammatory disease

Janset Onyuru, Lori Broderick, Christian Stehlik, Sana Ismaeel et al.
Nature Communications
Inflammasome and immune disorders
article

TRIM21 facilitates inflammasome assembly and contributes to autoinflammatory disease

Janset Onyuru, Lori Broderick, Christian Stehlik, Sana Ismaeel, Jessica Carrière, Andrea Dorfleutner, Sonal Khare, Kaiden A. Sims, Chawon Yun, Vinícius Dantas Martins, Savita Devi, Huyen Nguyen, Lan H. Chu, Elisabeth Jäger, Hal M. Hoffman, Lucia de Almeida, Justin Ruiz, Jae Jin Chae, Hemisha Khatri, Daniel L. Kastner
article en

Abstract

Inflammasomes are cytosolic multiprotein complexes facilitating the maturation and release of the inflammatory cytokines interleukin (IL)-1β and IL-18 and pyroptosis. ASC (apoptosis-associated-speck-like protein containing a CARD) is the central inflammasome adaptor. ASC polymerization is crucial for inflammasome assembly, and ASC particle release propagates inflammasome responses to bystander cells. However, control of inflammasome and ASC particle assembly to limit chronic inflammation and the emergence of autoinflammatory diseases is still incompletely understood. Here, we show that the E3 ubiquitin ligase TRIM (tripartite-motif-containing protein) 21, a common autoantigen in autoimmune diseases, is involved in inflammasome assembly. Specifically, TRIM21 binds to and ubiquitinates ASC to facilitate ASC/NLRP3 interactions, ASC polymerization and the release of ASC/TRIM21-containing particles during pyroptosis in human and mouse macrophages. Furthermore, we detect systemic ASC/TRIM21 particles and autoantibodies in human and mouse autoinflammatory disease. Thus, our findings highlight a previously unrecognized role of TRIM21 as an inflammasome component and driver of autoinflammation.

Nature Communications
Northwestern University (US), Cedars-Sinai Medical Center (US), Lurie Children's Hospital (US), National Institutes of Health (US), University of Miami (US), University of Washington (US), Rady Children's Hospital-San Diego (US), National Human Genome Research Institute (US), Tempus Labs (United States) (US), Korea Center for Disease Control and Prevention (KR), Indian Institute of Technology Hyderabad (IN)
American Cancer Society, American Heart Association, National Cancer Institute, National Institute of Allergy and Infectious Diseases, National Institute of Diabetes and Digestive and Kidney Diseases
Good health and well-being
Openalex Percentile: Top 8%
Inflammasome and immune disorders
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