SIGIRR
Identifiers
AliasesSIGIRR, TIR8, single immunoglobulin and toll-interleukin 1 receptor (TIR) domain, IL-1R8, single Ig and TIR domain containing
External IDsOMIM: 605478 MGI: 1344402 HomoloGene: 36399 GeneCards: SIGIRR
Orthologs
SpeciesHumanMouse
Entrez

59307

24058

Ensembl

ENSG00000185187

ENSMUSG00000025494

UniProt

Q6IA17

Q9JLZ8

RefSeq (mRNA)

NM_001135053
NM_001135054
NM_021805

NM_023059
NM_001355055

RefSeq (protein)

NP_001128525
NP_001128526
NP_068577

NP_075546
NP_001341984

Location (UCSC)Chr 11: 0.41 – 0.42 MbChr 7: 140.67 – 140.68 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Single Ig IL-1-related receptor (SIGIRR), also called Toll/Interleukin-1 receptor 8 (TIR8) or Interleukin-1 receptor 8 (IL-1R8), is transmembrane protein encoded by gene SIGIRR, which modulate inflammation, immune response, and tumorigenesis of colonic epithelial cells.[5]

Gene

Human gene SIGIRR is localized on chromosome 11. It is composed of 10 exons spanning about 11 700 base pairs.[6] In mouse, this gene is on chromosome 7, where it is composed of 9 exons spanning about 9 400 base pairs.[7]

Structure

SIGIRR is 410 amino acids long protein. In contrast with other members of IL-1 receptor family it has got only 1 immunoglobulin (Ig) domain in its N terminal extracellular part instead of 3 Ig domains. After this domain, there is a transmembrane domain, which is anchored to the plasmatic membrane. It has got TIR domain and 95 amino acids long C terminal tail in the intracellular part, which is not present in other IL-1 receptor family members. Structure of the TIR domain is different in the case of SIGIRR. In its tertiary structure SIGIRR lacks amino acids Ser447 and Tyr536, which are important for IL-1R1 signalization. Instead of these amino acids SIGIRR contains Cys222 and Leu305. The functional importance of these differences is not known so far. Human and mouse SIGIRR protein sequences are 82%, identical and they are overall 23% identical with IL-1R1.[5][6] SIGIRR is extensively glycosylated on its extracellular domain, and loss of this modification impairs its function.[8]

Expression

SIGIRR is expressed in several epithelial tissues, particularly in epithelial cells of kidneys, digestive tract, liver, lungs, and in lymphoid organs.[6] It is also expressed in monocytes, B lymphocytes, T lymphocytes, dendritic cells, and NK cells. In general, its expression is downregulated during inflammation or infection.[5] Its reduced expression was also found in patients with chronic lymphoid leukemia,[9] or in cells from colonic cancer. In human cells from colonic cancer, there was observed an increased expression of one variant of SIGIRR. This variant lacks its exon 8, is not glycosylated and its function is impaired. It also inhibits glycosylation of Wild type variant a its transport to plasmatic membrane.[8]

One of the discovered transcription factor, which regulates the expression of SIGIRR, is SP1. It binds to the proximal part of the promoter of the SIGIRR gene and induce its transcription. Binding of SP1 on SIGIRR promoter is inhibited by the activation of p38 MAP kinase, which is activated through the TLR4 signalization. Treatment of mice with a small amount of lipopolysaccharide, which is a ligand of TLR4, causes reduction in SIGIRR expression.[10][11]

Function

SIGIRR negatively regulates the activation of the IL-1R1, IL18R1, IL-1R5/ST2, TLR4, TLR7, TLR3, TLR9, and TLR1/2 and inhibits activation of transcription factor NF-κB and JNK MAP kinase.[5]

SIGIRR interacts with IL-1R1 when it binds IL-1. N terminal extracellular immunoglobulin domain associates with IL-1R1 and blocks its heterodimerization with IL-1RAP. In addition, C terminal TIR domain of SIGIRR binds downstream elements of IL-1R1 signalization and prevents the constitution of the functional signalling complex. Deletion of these domains disrupts the regulation activity of SIGIRR.[12][13] SIGIRR uses a slightly different mechanism to regulate the activity of TLR4. It also binds to receptor complex around TLR4. TIR domain of SIGIRR is crucial for interaction with TLR4, and it also interacts with downstream elements of the TLR4 pathway. In contrast, the extracellular immunoglobulin domain of SIGIRR is dispensable for the inhibition of TLR4 signalling.[12] There are 2 mechanisms, which are proposed for explanation of this inhibition of the TLR4 pathway. First is that SIGIRR blocks the formation of signalling complex at activated TLR4 and the second is that SIGIRR prevents translocation of this signalization complex into a cytosol.[13][14] SIGIRR inhibits signal transduction by its interaction with TLRs, IL-1R1 and downstream signalling proteins, and in this manner, it participates in negative regulation of inflammation. SIGIRR also prevents homodimerization of MYD88,[15] and it also prevents signalization through adaptor protein TRIF, which is used, for example, by TLR3.[14]

Negative regulation of IL-1R pathway by SIGIRR has its effect on the differentiation of Th17 lymphocytes. IL-1 supports differentiation for Th17 lymphocytes and expression of transcription factors RORγt and IRF4. Treatment by this cytokine also activates mTOR kinase and promotes the proliferation of Th17 lymphocytes. SIGIRR-deficient T lymphocytes lack this negative regulation, and it favours mTOR-dependent differentiation and proliferation of Th17 lymphocytes.[16] SIGIRR also negatively regulates TLRs, IL-1R pathway, and following mTOR activation in intestinal epithelial cells. Ligands for TLRs in the intestine are mainly components of intestinal microflora. Its deficiency or expression of mutated form in these cells leads to the signalization, which promotes inflammation, proliferation and increases incidence of tumors and its size.[8][17][10]

SIGIRR as a coreceptor of IL-1R5 for IL-37 binding

SIGIRR takes part in mediating the anti-inflammatory IL-37 signalization. It interacts with IL-37, IL-18R1 and forms tripartite signaling complex. Activity of this complex transduce anti-inflammatory signal and is essential for manifestation of IL-37 activity. Upon this signalization it causes inhibition of components of NF-κB pathway, kinases mTOR, TAK1, FYN, p38, JNK, ERK and it also causes activation of phosphatase PTEN, kinase MER, transcription factor STAT3 and adaptor protein p62 (DOK1). Pre-treatment of mice by IL-37 before injection of lipopolysaccharide reduced examined levels of pro-inflammatory cytokines and, also reduced their weight loss and hypothermia. This protective effect of IL-37 was abolished by deletion of SIGIRR, reduction of its expression or neutralization of IL-37 by antibodies.[18][19]

In addition to the regulation of inflammation, IL-37 also affects metabolism. Stimulation of skeletal muscle cells by IL-37 increases level of AMP-dependent kinase, increases its activation and induces metabolic reprogramming. It causes increase of oxidative phosphorylation, Krebs cycle, nucleotide and amino acids metabolism, and decrease of inflammatory mediators levels. This response does not occur in case of SIGIRR deficiency[20]

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000185187 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000025494 - Ensembl, May 2017
  3. ↑ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ↑ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. 1 2 3 4 Molgora M, Supino D, Mantovani A, Garlanda C (January 2018). "Tuning inflammation and immunity by the negative regulators IL-1R2 and IL-1R8". Immunological Reviews. 281 (1): 233–247. doi:10.1111/imr.12609. PMC 5922415. PMID 29247989.
  6. 1 2 3 Thomassen E, Renshaw BR, Sims JE (June 1999). "Identification and characterization of SIGIRR, a molecule representing a novel subtype of the IL-1R superfamily". Cytokine. 11 (6): 389–99. doi:10.1006/cyto.1998.0452. PMID 10346978.
  7. ↑ "Sigirr single immunoglobulin and toll-interleukin 1 receptor (TIR) domain [Mus musculus (house mouse)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2021-01-24.
  8. 1 2 3 Zhao J, Bulek K, Gulen MF, Zepp JA, Karagkounis G, Martin BN, et al. (December 2015). "Human Colon Tumors Express a Dominant-Negative Form of SIGIRR that Promotes Inflammation and Colitis-Associated Colon Cancer in Mice". Gastroenterology. 149 (7): 1860–1871.e8. doi:10.1053/j.gastro.2015.08.051. PMC 5308447. PMID 26344057.
  9. ↑ Vilia MG, Fonte E, Veliz Rodriguez T, Tocchetti M, Ranghetti P, Scarfò L, et al. (October 2017). "The inhibitory receptor toll interleukin-1R 8 (TIR8/IL-1R8/SIGIRR) is downregulated in chronic lymphocytic leukemia". Leukemia & Lymphoma. 58 (10): 2419–2425. doi:10.1080/10428194.2017.1295142. PMID 28278705. S2CID 11804905.
  10. 1 2 Kadota C, Ishihara S, Aziz MM, Rumi MA, Oshima N, Mishima Y, et al. (November 2010). "Down-regulation of single immunoglobulin interleukin-1R-related molecule (SIGIRR)/TIR8 expression in intestinal epithelial cells during inflammation". Clinical and Experimental Immunology. 162 (2): 348–61. doi:10.1111/j.1365-2249.2010.04254.x. PMC 2996602. PMID 21077278.
  11. ↑ Ueno-Shuto K, Kato K, Tasaki Y, Sato M, Sato K, Uchida Y, et al. (June 2014). "Lipopolysaccharide decreases single immunoglobulin interleukin-1 receptor-related molecule (SIGIRR) expression by suppressing specificity protein 1 (Sp1) via the Toll-like receptor 4 (TLR4)-p38 pathway in monocytes and neutrophils". The Journal of Biological Chemistry. 289 (26): 18097–109. doi:10.1074/jbc.m113.532093. PMC 4140261. PMID 24821721.
  12. 1 2 Qin J, Qian Y, Yao J, Grace C, Li X (July 2005). "SIGIRR inhibits interleukin-1 receptor- and toll-like receptor 4-mediated signaling through different mechanisms". The Journal of Biological Chemistry. 280 (26): 25233–41. doi:10.1074/jbc.m501363200. PMID 15866876.
  13. 1 2 Wald D, Qin J, Zhao Z, Qian Y, Naramura M, Tian L, et al. (September 2003). "SIGIRR, a negative regulator of Toll-like receptor-interleukin 1 receptor signaling". Nature Immunology. 4 (9): 920–7. doi:10.1038/ni968. PMID 12925853. S2CID 25246605.
  14. 1 2 Guven-Maiorov E, Keskin O, Gursoy A, Nussinov R (September 2015). "A Structural View of Negative Regulation of the Toll-like Receptor-Mediated Inflammatory Pathway". Biophysical Journal. 109 (6): 1214–26. Bibcode:2015BpJ...109.1214G. doi:10.1016/j.bpj.2015.06.048. PMC 4576153. PMID 26276688.
  15. ↑ Gong J, Wei T, Stark RW, Jamitzky F, Heckl WM, Anders HJ, et al. (March 2010). "Inhibition of Toll-like receptors TLR4 and 7 signaling pathways by SIGIRR: a computational approach". Journal of Structural Biology. 169 (3): 323–30. doi:10.1016/j.jsb.2009.12.007. PMID 20025973.
  16. ↑ Gulen MF, Kang Z, Bulek K, Youzhong W, Kim TW, Chen Y, et al. (January 2010). "The receptor SIGIRR suppresses Th17 cell proliferation via inhibition of the interleukin-1 receptor pathway and mTOR kinase activation". Immunity. 32 (1): 54–66. doi:10.1016/j.immuni.2009.12.003. PMC 3015141. PMID 20060329.
  17. ↑ Xiao H, Yin W, Khan MA, Gulen MF, Zhou H, Sham HP, et al. (August 2010). "Loss of single immunoglobulin interlukin-1 receptor-related molecule leads to enhanced colonic polyposis in Apc(min) mice". Gastroenterology. 139 (2): 574–85. doi:10.1053/j.gastro.2010.04.043. PMC 3261756. PMID 20416302.
  18. ↑ Nold-Petry CA, Lo CY, Rudloff I, Elgass KD, Li S, Gantier MP, et al. (April 2015). "IL-37 requires the receptors IL-18Rα and IL-1R8 (SIGIRR) to carry out its multifaceted anti-inflammatory program upon innate signal transduction". Nature Immunology. 16 (4): 354–65. doi:10.1038/ni.3103. PMID 25729923. S2CID 24578661.
  19. ↑ Li S, Neff CP, Barber K, Hong J, Luo Y, Azam T, et al. (February 2015). "Extracellular forms of IL-37 inhibit innate inflammation in vitro and in vivo but require the IL-1 family decoy receptor IL-1R8". Proceedings of the National Academy of Sciences of the United States of America. 112 (8): 2497–502. Bibcode:2015PNAS..112.2497L. doi:10.1073/pnas.1424626112. PMC 4345608. PMID 25654981.
  20. ↑ Cavalli G, Justice JN, Boyle KE, D'Alessandro A, Eisenmesser EZ, Herrera JJ, et al. (February 2017). "Interleukin 37 reverses the metabolic cost of inflammation, increases oxidative respiration, and improves exercise tolerance". Proceedings of the National Academy of Sciences of the United States of America. 114 (9): 2313–2318. Bibcode:2017PNAS..114.2313C. doi:10.1073/pnas.1619011114. PMC 5338542. PMID 28193888.

Further reading

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