RRC ID 86321
著者 Lee J, Sasaki F, Koike E, Cho M, Lee Y, Dho SH, Lee J, Lee E, Toyohara E, Sunakawa M, Ishibashi M, Hung HH, Nishioka S, Komine R, Okura C, Shimizu M, Ikawa M, Yoshimura A, Morita R, Kim LK.
タイトル Gelsolin alleviates rheumatoid arthritis by negatively regulating NLRP3 inflammasome activation.
ジャーナル Cell Death Differ
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.
巻・号 31(12)
ページ 1679-1694
公開日 2024-12-1
DOI 10.1038/s41418-024-01367-6
PII 10.1038/s41418-024-01367-6
PMID 39179640
PMC PMC11618363
MeSH Animals Arthritis, Rheumatoid* / metabolism Arthritis, Rheumatoid* / pathology Gelsolin* / genetics Gelsolin* / metabolism Humans Inflammasomes* / metabolism Lipopolysaccharides / pharmacology Macrophages / metabolism Male Mice Mice, Inbred C57BL Mice, Knockout* Mitochondria / drug effects Mitochondria / metabolism NLR Family, Pyrin Domain-Containing 3 Protein* / metabolism
IF 10.717
リソース情報
ヒト・動物細胞 J774.1