| 1999 |
SIGIRR was identified as a novel member of the IL-1R superfamily with a single extracellular Ig domain and an unusually long cytoplasmic domain. It failed to bind known IL-1 family ligands and a chimeric construct fusing the SIGIRR intracellular domain to the IL-1R extracellular domain did not activate NF-κB, establishing that the SIGIRR intracellular domain lacks signaling capacity. |
Chimeric receptor expression, NF-κB reporter assay, ligand binding assay |
Cytokine |
Medium |
10346978
|
| 2003 |
SIGIRR functions as a negative regulator of TLR-IL-1R signaling; it binds to TLR/IL-1R signaling components (IL-1R, MyD88, IRAK, TRAF6) in a ligand-dependent manner, and SIGIRR-deficient mice show enhanced chemokine induction after IL-1 injection and reduced threshold for lethal endotoxin challenge. |
Co-immunoprecipitation (endogenous), SIGIRR-knockout mouse model with cytokine/chemokine readouts |
Nature immunology |
High |
12925853
|
| 2003 |
The intracellular TIR domain of SIGIRR is required for inhibiting IL-1 signaling, while the extracellular Ig domain is dispensable for blocking NF-κB activation in an IL-1R reporter system. |
NF-κB reporter assay with truncation mutants |
European cytokine network |
Medium |
14715412
|
| 2004 |
TIR8/SIGIRR acts as an intracellular decoy for TLR/IL-1R signaling components; TIR8-deficient dendritic cells show increased cytokine production in response to TLR agonists (LPS, CpG), and TIR8-deficient mice are more susceptible to intestinal inflammation, demonstrating a cell-type-specific inhibitory role. |
TIR8-knockout mouse model, DC stimulation assays |
Proceedings of the National Academy of Sciences of the United States of America |
High |
14993616
|
| 2005 |
SIGIRR inhibits IL-1 and LPS signaling through distinct mechanisms: the extracellular Ig domain is required to block IL-1 signaling by interfering with IL-1R/IL-1RAcP heterodimerization, while the intracellular TIR domain inhibits both IL-1 and LPS signaling by attenuating recruitment of MyD88, IRAK, and TRAF6 to the receptor complex. Deletion of the TIR domain (ΔTiR) abrogates inhibition of both pathways; deletion of the Ig domain (ΔN) abrogates inhibition of IL-1 but not LPS signaling. |
Deletion mutagenesis, endogenous Co-immunoprecipitation, NF-κB reporter assay |
The Journal of biological chemistry |
High |
15866876
|
| 2007 |
Epithelium-derived SIGIRR is critical for controlling colonic homeostasis and innate immune responses; gut epithelium-specific transgenic rescue of SIGIRR in SIGIRR-deficient mice reduced DSS-induced colitis and AOM+DSS-induced tumorigenesis, placing SIGIRR function in the intestinal epithelial compartment. |
Tissue-specific transgenic rescue in SIGIRR-KO mice, DSS/AOM chemical colitis model |
Immunity |
High |
17398123
|
| 2009 |
SIGIRR forms a complex with ST2 upon IL-33 stimulation and specifically inhibits IL-33/ST2-mediated NF-κB and MAPK signaling; SIGIRR-deficient mice show enhanced IL-33-induced Th2 responses and airway inflammation. |
Co-immunoprecipitation, SIGIRR-KO mouse model, IL-33-induced Th2 and asthma models |
Journal of immunology |
High |
19234154
|
| 2009 |
Computational structural modeling of the SIGIRR TIR domain predicts that SIGIRR inhibits TLR4 and TLR7 signaling by blocking the molecular interface between TLR and MyD88 adaptor, primarily via its BB-loop region. |
Homology modeling, protein-protein docking (computational) |
Journal of structural biology |
Low |
20025973
|
| 2010 |
SIGIRR governs Th17 cell differentiation and expansion by suppressing IL-1-induced JNK and mTOR kinase activation; SIGIRR-deficient T cells show enhanced Th17 polarization and IL-1-induced proliferation that is abolished by mTOR deficiency, placing SIGIRR upstream of mTOR in IL-1 signaling in T cells. |
SIGIRR-KO mouse model, in vitro Th17 polarization, phospho-signaling (JNK, mTOR), mTOR-KO epistasis |
Immunity |
High |
20060329
|
| 2010 |
LPS down-regulates SIGIRR expression in intestinal epithelial cells through decreased binding of the transcription factor SP1 to the SIGIRR promoter, as demonstrated by gel-shift and chromatin immunoprecipitation assays; inflammatory cytokines TNF-α and LPS reduced SIGIRR mRNA in IECs. |
EMSA (gel shift), chromatin immunoprecipitation (ChIP), siRNA knockdown, flow cytometry |
Clinical and experimental immunology |
Medium |
21077278
|
| 2010 |
SIGIRR inhibits TLR4, TLR5, and TLR9-mediated inflammatory cytokine production in human airway epithelial cells by sequestering the adaptor MyD88, preventing its recruitment to these TLRs, as shown by co-immunoprecipitation. |
Co-immunoprecipitation, SIGIRR overexpression, cytokine measurement |
Molecular biology reports |
Medium |
20364327
|
| 2011 |
Absence of SIGIRR in the hippocampus leads to increased expression of IL-1RI and TLR4 and upregulation of downstream IRAK1, JNK, and NF-κB; cognitive deficits and LTP impairment in SIGIRR-KO mice are attenuated by IL-1ra, anti-TLR4 antibody, and JNK/NF-κB inhibitors, demonstrating that SIGIRR suppresses IL-1α/IL-1RI and HMGB1/TLR4 signaling in hippocampal neurons. |
SIGIRR-KO mouse model, pharmacological rescue (IL-1ra, anti-TLR4 Ab, kinase inhibitors), LTP electrophysiology, western blot |
The Journal of neuroscience |
High |
21389242
|
| 2014 |
LPS down-regulates SIGIRR expression in monocytes and neutrophils via the TLR4-p38 MAPK pathway, which suppresses SP1-mediated transactivation of the SIGIRR proximal promoter; dominant-negative TLR4 and p38 siRNA each blocked LPS-induced SIGIRR down-regulation, and ChIP/reporter assays confirmed SP1 binding at the SIGIRR promoter. |
Dominant-negative receptor expression, siRNA, reporter gene assay, ChIP, p38 activator (anisomycin) |
The Journal of biological chemistry |
High |
24821721
|
| 2015 |
IL-37 requires the co-receptor IL-1R8 (SIGIRR) and IL-18Rα to form a tripartite receptor complex on the surface of PBMCs upon LPS stimulation; silencing of IL-1R8 or IL-18Rα impairs IL-37 anti-inflammatory activity. IL-37 uses IL-1R8 to harness Mer, PTEN, STAT3, p62(dok), and to inhibit Fyn, TAK1, NF-κB, and MAPKs, and exerts a pseudo-starvational effect on mTOR. |
Proteomic/transcriptomic analysis, siRNA knockdown of IL-1R8/IL-18Rα, IL-1R8-KO mouse crossed with IL-37tg, surface complex detection |
Nature immunology |
High |
25729923
|
| 2015 |
Recombinant IL-37 binds directly to the IL-18 receptor α-chain and to the decoy receptor IL-1R8; IL-37 anti-inflammatory effects on dendritic cells are abolished in IL-1R8-deficient DCs, establishing IL-1R8 as required for extracellular IL-37 function. |
Direct binding assay (immobilized receptor), IL-1R8-KO DC functional assay, cytokine measurement |
Proceedings of the National Academy of Sciences of the United States of America |
High |
25654981
|
| 2015 |
Human colon tumors express a dominant-negative splice isoform of SIGIRR (SIGIRR-ΔE8) that lacks complex glycosylation and is retained in the cytoplasm; SIGIRR-ΔE8 interacts with full-length SIGIRR, reduces its glycosylation, and prevents its localization to the cell surface, thereby blocking its ability to inhibit IL-1R signaling. A glycosylation-null mutant SIGIRR(N86/102S) expressed in mouse colonic epithelium phenocopies loss-of-function. |
RNA sequencing, immunoblot, immunofluorescence, co-immunoprecipitation, transgenic mouse (N86/102S mutant), AOM/DSS model |
Gastroenterology |
High |
26344057
|
| 2015 |
SIGIRR variants identified in human NEC infants (p.Y168X stop mutation and p.S80Y missense) result in loss of SIGIRR function and exaggerated LPS-induced inflammation in HEK293 and intestinal epithelial cells, establishing the functional consequence of these human variants. |
Exome sequencing, expression of variant constructs in HEK293 and IEC, NF-κB/cytokine reporter assays |
Pediatrics |
Medium |
25963006
|
| 2016 |
IL-1R8 serves as a checkpoint for NK cell maturation and effector function; genetic blockade of IL-1R8 unleashes NK cell-mediated resistance to hepatic carcinogenesis, haematogenous liver and lung metastasis, and cytomegalovirus infection in mice. |
IL-1R8-KO mouse model, NK cell depletion/transfer, tumor and viral infection models |
Nature |
High |
29072292
|
| 2016 |
IL-1R8 is expressed at high levels on human and mouse platelets and megakaryocytes; IL-1R8-deficient mice show increased platelet activation (homotypic and heterotypic aggregation, P-selectin exposure) in response to ADP, IL-1, and LPS, with increased thromboembolism, and this hyperactivity is abrogated by commensal flora depletion or IL-1R1 deficiency. |
Flow cytometry, western blot, confocal microscopy, IL-1R8-KO mouse, platelet aggregation assays, in vivo thromboembolism model, genetic epistasis (IL-1R1 KO) |
Cardiovascular research |
High |
27297888
|
| 2017 |
Lack of IL-1R8 in neurons causes hyperactivation of the IL-1 signaling pathway, leading to up-regulation of the mTOR pathway and increased levels of the epigenetic regulator MeCP2, disrupting dendritic spine morphology, synaptic plasticity, and gene expression; genetic correction of MeCP2 in IL-1R8-KO neurons rescues synaptic defects, and pharmacological IL-1R blockade (Anakinra) restores MeCP2 levels and cognition. |
IL-1R8-KO mouse model, MeCP2 genetic correction, Anakinra pharmacological rescue, spine morphology, LTP, transcriptomics |
eLife |
High |
28347403
|
| 2019 |
IL-1R8/Sigirr protein stability is regulated by the ubiquitin-proteasome system through site-specific ubiquitination; the deubiquitinase USP13 antagonizes this degradation by directly stabilizing IL-1R8. USP13-deficient cells showed increased IL-1R8 poly-ubiquitination and reduced stability, enhanced TLR4 signaling, and IL-1R8 overexpression rescued the USP13-/- inflammatory phenotype. |
Ubiquitination assay, USP13 knockdown/KO, receptor ligation-chase model, overexpression rescue, in vivo lung injury model |
EBioMedicine |
High |
31204278
|
| 2021 |
IL-37-induced degradation of IL-1R8/Sigirr is mediated by GSK3β-dependent phosphorylation at threonine-372; GSK3β associates with residues 51-101 of Sigirr, phosphorylates it at T372 upon IL-37 stimulation, promoting Sigirr internalization, dissociation from USP13, and proteasomal degradation. The T372 mutant resists IL-37-induced degradation. |
Co-immunoprecipitation, site-directed mutagenesis (T372A), GSK3β inhibition, kinase domain mapping, Sigirr internalization assay |
Journal of cellular physiology |
High |
33400290
|
| 2021 |
SIGIRR activates STAT3-dependent expression of miR-146a and miR-155 in intestinal epithelial cells; this pathway represses IRAK1, contributing to postnatal gut immune tolerance. A human NEC-associated SIGIRR stop mutation (p.Y168X) disrupts SIGIRR-STAT3-miRNA signaling, increasing IRAK1 expression, as confirmed by ChIP and luciferase assays. |
CRISPR/Cas9 knock-in mouse (p.Y168X), ChIP, luciferase reporter, siRNA, western blot, qRT-PCR |
Cellular and molecular gastroenterology and hepatology |
High |
34563711
|
| 2016 |
Zebrafish SIGIRR (DrSIGIRR) interacts with the TRIF adaptor protein and inhibits TRIF-mediated NF-κB activation downstream of TLR3/TLR22; pull-down and Duolink proximity ligation assays demonstrated direct DrSIGIRR-TRIF interaction, and DrSIGIRR knockdown promoted poly(I:C)-induced hepatic inflammation. |
Pull-down assay, Duolink in situ proximity ligation assay, siRNA knockdown in zebrafish, NF-κB reporter, histology |
Journal of immunology |
Medium |
27206770
|
| 2010 |
The BB-loop deletion of SIGIRR's intracellular TIR domain completely abrogates SIGIRR's inhibitory effect on TLR7 signaling; structure modeling positions the BB-loop as the key interface for interaction with TLR7 and MyD88. |
BB-loop deletion mutagenesis (functional reporter assay), computational structure prediction |
The Journal of pathology |
Medium |
20112371
|
| 2020 |
SIGIRR negatively regulates TRAF6 ubiquitination; SIGIRR knockdown enhances TRAF6 expression and increases NF-κB activity via the classical NF-κB pathway in alveolar epithelial and macrophage cells. |
siRNA knockdown, ubiquitination assay, NF-κB reporter, cytokine measurement |
Journal of immunology research |
Medium |
33123603
|
| 2022 |
SIGIRR promotes instability of CD18 protein in alveolar macrophages by enhancing its ubiquitination and proteasomal degradation; CD18 deletion abolishes the anti-inflammatory therapeutic effect of SIGIRR overexpression in LPS-induced acute lung injury, establishing a SIGIRR/CD18 regulatory circuit. |
SIGIRR lentiviral overexpression, CD18-KO mouse, ubiquitination assay, intratracheal LPS model, macrophage adhesion and inflammasome assays |
The FEBS journal |
High |
36527283
|
| 2023 |
IL-37 directly inhibits platelet activation by binding to platelet IL-1R8 and IL-18Rα; using platelet-specific IL-1R8-deficient mice, IL-37 was shown to combine with IL-1R8 to enhance PTEN activity and thereby inhibit Akt, MAPK, and SYK pathways, reducing reactive oxygen species and platelet aggregation. |
Platelet-specific IL-1R8-KO mouse, PTEN-KO platelets, PTEN inhibitor, FeCl3 thrombosis model, microfluidic perfusion assay, signaling biochemistry |
Circulation research |
High |
36999436
|
| 2020 |
SIGIRR associates with MyD88 in both Chlamydia trachomatis-infected and uninfected epithelial cells; loss of SIGIRR leads to increased IL-8 production upon C. trachomatis infection, establishing SIGIRR as a negative regulator of TLR/MyD88-dependent responses to this pathogen. |
Co-immunoprecipitation, siRNA knockdown, SIGIRR overexpression, IL-8 ELISA |
PloS one |
Medium |
32210474
|
| 2024 |
IL-38 inhibits NLRP3 inflammasome activation in cardiac fibroblasts through IL-1R8; IL-38 reduces SYK phosphorylation in an IL-1R8-dependent manner, and silencing of IL-1R8 abolishes IL-38's suppressive effect on the NLRP3 inflammasome. |
siRNA knockdown of IL-1R8, NLRP3 inhibitor, hypoxia/reoxygenation model, MIRI mouse model, SYK phosphorylation assay |
International immunopharmacology |
Medium |
39447412
|
| 2022 |
SIGIRR deficiency in memory CD4 T cells unleashes the IL-1/C/EBPβ/TNF-α signaling axis; ectopic SIGIRR expression in memory CD4 T cells reduces TNF-α production, and CD4 T cell transfer from SIGIRR-KO mice exacerbates antigen-induced arthritis, placing SIGIRR upstream of C/EBPβ-driven TNF-α transcription. |
SIGIRR-KO mouse, CD4 T cell adoptive transfer, SIGIRR overexpression, siRNA, immunoblot, bioinformatics cis-regulatory analysis |
Molecular medicine |
Medium |
36401167
|
| 2007 |
Cell-type-specific regulation and function of TIR8/SIGIRR was demonstrated: TIR8 expressed on resident intrarenal myeloid cells (not tubular epithelial cells) suppresses TLR-mediated chemokine expression; TIR8 is induced by LPS/TNF/IFN-γ in monocytes but downregulated in tubular epithelial cells, and N- and O-glycosylation differs between myeloid and non-myeloid renal cells. |
Cell fractionation, KO mouse, myeloid-specific functional assays, glycosylation analysis |
Kidney international |
Medium |
17495864
|
| 2021 |
IL-37 inhibits SIGIRR-dependent CD8+ T cell function: IL-37 antagonizes IL-18-induced proliferation and effector function of CD8+ T cells in a SIGIRR-dependent manner, promoting tumor immune evasion in colorectal cancer models. |
IL-37tg mouse, SIGIRR-KO epistasis, CD8+ T cell functional assays (proliferation, cytotoxicity, cytokine production), B16-OVA tumor model |
Signal transduction and targeted therapy |
Medium |
35046386
|