Evidence map›Paper›PMID 39179640›Full record

ArticleCell death and differentiation2024

Gelsolin alleviates rheumatoid arthritis by negatively regulating NLRP3 inflammasome activation.

Jiyeon Lee, Fumiyuki Sasaki, Eri Koike, Minjeong Cho, Yeongun Lee, So Hee Dho, Jina Lee, Eunji Lee, Eri Toyohara, Mika Sunakawa and 10 more

Abstract read
In one paragraph

Article in Cell death and differentiation, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Trial
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  13. Aquaporins in sepsis- an update.Frontiers in immunology · 2024
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Jiyeon LeeDepartment of Biomedical Sciences, Graduate School of Medical Science, Brain Korea 21 Project, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
Fumiyuki SasakiDepartment of Microbiology and Immunology, Nippon Medical School, Tokyo, Japan.
Eri KoikeDepartment of Microbiology and Immunology, Nippon Medical School, Tokyo, Japan.
Minjeong ChoDepartment of Biomedical Sciences, Graduate School of Medical Science, Brain Korea 21 Project, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
Yeongun LeeDepartment of Biomedical Sciences, Graduate School of Medical Science, Brain Korea 21 Project, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
So Hee DhoDepartment of Biomedical Sciences, Graduate School of Medical Science, Brain Korea 21 Project, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
Jina LeeDepartment of Biomedical Sciences, Graduate School of Medical Science, Brain Korea 21 Project, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
Eunji LeeDepartment of Biomedical Sciences, Graduate School of Medical Science, Brain Korea 21 Project, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
Eri ToyoharaDepartment of Microbiology and Immunology, Nippon Medical School, Tokyo, Japan.
Mika SunakawaDepartment of Microbiology and Immunology, Nippon Medical School, Tokyo, Japan.
Mariko IshibashiDepartment of Microbiology and Immunology, Nippon Medical School, Tokyo, Japan.
Huynh Hiep HungDepartment of Microbiology and Immunology, Nippon Medical School, Tokyo, Japan.
Saki NishiokaImmunology Frontier Research Center, Osaka University, Suita, Japan.
Ritsuko KomineDepartment of Microbiology and Immunology, Keio University School of Medicine, Tokyo, Japan.
Chiaki OkuraDepartment of Microbiology and Immunology, Keio University School of Medicine, Tokyo, Japan.
Masumi ShimizuDepartment of Microbiology and Immunology, Nippon Medical School, Tokyo, Japan.
Masahito IkawaImmunology Frontier Research Center, Osaka University, Suita, Japan.ORCID 0000-0001-9859-6217
Akihiko YoshimuraDepartment of Microbiology and Immunology, Keio University School of Medicine, Tokyo, Japan.
Rimpei MoritaDepartment of Microbiology and Immunology, Nippon Medical School, Tokyo, Japan. rimpei-morita@nms.ac.jp.
Lark Kyun KimDepartment of Biomedical Sciences, Graduate School of Medical Science, Brain Korea 21 Project, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea. LKKIM@yuhs.ac.ORCID 0000-0001-5983-4470

Funding

MEXT | Japan Society for the Promotion of Science (JSPS) 16H05178MEXT | Japan Society for the Promotion of Science (JSPS) 22K07140National Research Foundation of Korea (NRF) NRF- 2022M3A9B6017424National Research Foundation of Korea (NRF) NRF-2023R1A2C1005804National Research Foundation of Korea (NRF) RS-2024-00408822
6 · The paper itself

Abstract

Despite numerous biomarkers being proposed for rheumatoid arthritis (RA), a gap remains in our understanding of their mechanisms of action. In this study, we discovered a novel role for gelsolin (GSN), an actin-binding protein whose levels are notably reduced in the plasma of RA patients. We elucidated that GSN is a key regulator of NLRP3 inflammasome activation in macrophages, providing a plausible explanation for the decreased secretion of GSN in RA patients. We found that GSN interacts with NLRP3 in LPS-primed macrophages, hence modulating the formation of the NLRP3 inflammasome complex. Reducing GSN expression significantly enhanced NLRP3 inflammasome activation. GSN impeded NLRP3 translocation to the mitochondria; it contributed to the maintenance of intracellular calcium equilibrium and mitochondrial stability. This maintenance is crucial for controlling the inflammatory response associated with RA. Furthermore, the exacerbation of arthritic symptoms in GSN-deficient mice indicates the potential of GSN as both a diagnostic biomarker and a therapeutic target. Moreover, not limited to RA models, GSN has demonstrated a protective function in diverse disease models associated with the NLRP3 inflammasome. Myeloid cell-specific GSN-knockout mice exhibited aggravated inflammatory responses in models of MSU-induced peritonitis, folic acid-induced acute tubular necrosis, and LPS-induced sepsis. These findings suggest novel therapeutic approaches that modulate GSN activity, offering promise for more effective management of RA and a broader spectrum of inflammatory conditions.

Indexed as

Arthritis, RheumatoidGelsolinInflammasomesMice, KnockoutNLR Family, Pyrin Domain-Containing 3 ProteinAnimalsHumansLipopolysaccharidesMacrophagesMaleMiceMice, Inbred C57BLMitochondriaGelsolinInflammasomesLipopolysaccharidesNLR Family, Pyrin Domain-Containing 3 ProteinNLRP3 protein, humanNlrp3 protein, mouse

Identifiers

PMID39179640
PMCPMC11618363

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.