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IL22RA2

From Wikipedia, the free encyclopedia
interleukin 22 receptor, alpha 2
Identifiers
SymbolIL22RA2
NCBI gene116379
HGNC14901
OMIM606648
RefSeqNM_181310
UniProtQ969J5
Other data
LocusChr. 6 q24.1-24.2
Search for
StructuresSwiss-model
DomainsInterPro

Interleukin-22 receptor subunit alpha-2 (IL-22RA2), also known as interleukin-22 binding protein (IL-22BP) is a naturally secreted monomeric protein acting as an interleukin-22 (IL-22) antagonist with inhibitory effects on IL-22 activity in vivo. IL-22BP is in humans encoded by the IL22RA2 gene located on chromosome 6, and in mice is encoded by the il22ra2 gene located on chromosome 10. IL-22BP belongs to the class II cytokine receptor family and it is a soluble receptor homolog of IL-22R (aliases IL-22RA1/IL-22RA/IL-22R1).[1][2]

The main function of IL-22BP is the regulation of IL-22 biological activity through specific binding which blocks the interaction of IL-22 with its cell surface receptor IL-22R and thus prevents the downstream cellular signalling and response. IL-22 and IL-22BP interactions play an important role in health and disease and are involved in the regulation of steady-state homeostasis,[1] inflammatory responses[3] and cancer.[4]

Structure and interaction

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IL-22BP is a soluble monomeric cytokine receptor protein. IL-22BP shares approximately 34% sequence homology with the extracellular domain of one subunit of the heterodimeric membrane-bound IL-22R, which is the main cellular receptor for IL-22 providing the subsequent signalling. This homology extends to the secondary and tertiary structure of the proteins allowing specific binding and protein-protein interactions. IL-22BP also shares homology with other related cytokine receptors IL-10RB, and IL-20RA. IL-22BP is a secreted protein that lacks both transmembrane and intracellular domains, it contains two tandem fibronectin-III domains, glycosylation sites and four conserved cysteine residues. The molecular mass of secreted IL-22BP is approximately 30 kDa.[2][5]

IL-22BP with its five binding loops contacts IL-22 at the site overlapping the IL-22R binding site, successfully blocking the IL-22-IL-22R interaction. The dissociation constant KD for IL-22-IL-22BP is ~ 1 pM highlighting very tight interaction and high affinity, whereas KD for IL-22-IL-22R is only ~ 20 nM meaning much lower affinity. Also, the Koff dissociation rate for the IL22BP-IL-22 complex is over 4 days but Koff dissociation rate for the IL-22R-IL-22 complex is only a few minutes. These chemical properties ensure that IL-22 which is bound to IL-22BP is effectively sequestered from interaction with IL-22R.[6][7]

Function and regulation

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Similarly to the expression profile of IL-22, IL-22BP is expressed in lymphoid and barrier tissues such as the spleen, mesenteric lymph nodes, gastrointestinal tract, skin, lungs, and liver among others. IL-22BP is produced by dendritic cells, particularly by specialised intestinal dendritic cell populations.[8][9] Other identified cellular sources of IL-22BP include eosinophils,[10] CD4+ TH lymphocytes[11] and keratinocytes.[12]

The detailed role of IL-22BP-IL-22 interactions is so far the best described in the gastrointestinal tract, where IL-22BP helps to maintain homeostasis and tolerance regulating IL-22 bioavailability. In the gastrointestinal tract, the levels of these two molecules are inverse during different immunological conditions. In healthy, steady-state homeostasis, the levels of IL-22BP are the highest and decrease rapidly during immune response and inflammation when high levels of IL-22 are produced. Inflammation mediators such as prostaglandin E2 (PGE2),[8] IL-18 and other inflammasome components[4] are known to downregulate IL-22BP production, on the other hand, the presence of retinoic acid, metabolite of vitamin A, is known to induce IL-22BP secretion.[8] IL-22BP in the gut is also involved in enabling proper antigen sampling from the intestinal lumen to intestinal lymphoid tissues, which is crucial for maintaining tolerance and homeostasis. Further IL-22BP regulates lipid adsorption and proliferation of intestinal epithelial cells.[13]

To a less extent, the function of IL-22BP is described in other tissues such as skin,[12] lungs[3] and liver. In most of these tissues, IL-22BP is thought to have protective effects. However, as it regulates the dual-natured IL-22 cytokine, which can have both protective and pathological effects, IL-22BP can also have both pro- and anti-inflammatory effects depending on many various conditions and stimuli. The detailed role and involvement of IL-22BP in the health and disease of different tissues remain to be fully explained.[1]

Disease and therapy

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As the function of IL-22BP implies, in general, the presence of IL-22BP has a positive/protective effect on the diseases that are exacerbated by IL-22 activity and vice versa. Dysfunctional IL-22BP-IL-22 interactions have been among other molecules linked to the development inflammatory diseases of the gastrointestinal tract such as inflammatory bowel disease (IBD) and its components Crohn's disease (CD) and ulcerative colitis (UC).[1] It was reported that IBD patients harbour elevated levels of both IL-22BP and IL-22 when compared to healthy controls, suggesting that in the context of chronic inflammation the effects of these molecules can be dramatically changed from the healthy state.[11][8] Another research study working with il22ra2 knockout mouse model pointed out protective role of IL-22BP in the tumorigenesis of colorectal cancer (CRC) as animals of this genotype had increased tumour formation when compared to wild-type controls.[4] In addition to these observations, it has also been proposed that the anti-tumour effects of lymphotoxin α and β could be mediated in IL-22BP dependent manner.[14]

In lung infection studies with influenza virus and Streptococcus pneumoniae the observed effects of IL-22BP were mostly negative and exacerbated infection-induced pneumonia due to reduced levels of active protective IL-22 on epithelial tight junctions and antimicrobial peptides secretion.[3][15] In mice with experimental autoimmune encephalomyelitis (EAE) which is a model of multiple sclerosis (MS) negative effects of IL-22BP on the disease progression were observed, partially due to insufficient repression of pro-inflammatory IFNγ levels by neutralised IL-22.[16]

IL-22 is a target molecule for the development of novel therapies to treat chronic inflammatory diseases in which the IL-22 biological pathway is thought to be involved, such as the UC, acute graft versus host disease (GVHD), psoriasis and COVID-19 among others.[1] Targeting IL-22BP biology in these therapies can also be beneficial, for example, the use of IL-22BP in a similar fashion as manufactured neutralizing monoclonal antibodies against IL-22 is being studied. Novel research is pointing in the direction of using IL-22BP as a potential biomarker for CRC and anti-TNFα IBD therapy prognosis.[4][11]

References

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  1. ^ a b c d e Zenewicz LA (2021-11-16). "IL-22 Binding Protein (IL-22BP) in the Regulation of IL-22 Biology". Frontiers in Immunology. 12: 766586. doi:10.3389/fimmu.2021.766586. PMC 8634938. PMID 34868019.
  2. ^ a b Dumoutier L, Lejeune D, Colau D, Renauld JC (June 2001). "Cloning and characterization of IL-22 binding protein, a natural antagonist of IL-10-related T cell-derived inducible factor/IL-22". Journal of Immunology. 166 (12): 7090–7095. doi:10.4049/jimmunol.166.12.7090. PMID 11390453. S2CID 32473644.
  3. ^ a b c Hebert KD, Mclaughlin N, Galeas-Pena M, Zhang Z, Eddens T, Govero A, et al. (January 2020). "Targeting the IL-22/IL-22BP axis enhances tight junctions and reduces inflammation during influenza infection". Mucosal Immunology. 13 (1): 64–74. doi:10.1038/s41385-019-0206-9. PMC 6917921. PMID 31597930.
  4. ^ a b c d Huber S, Gagliani N, Zenewicz LA, Huber FJ, Bosurgi L, Hu B, et al. (November 2012). "IL-22BP is regulated by the inflammasome and modulates tumorigenesis in the intestine". Nature. 491 (7423): 259–263. Bibcode:2012Natur.491..259H. doi:10.1038/nature11535. PMC 3493690. PMID 23075849.
  5. ^ Watanabe L, de Moura PR, Nascimento AS, Colau D, Dumoutier L, Renauld JC, Polikarpov I (February 2009). "Crystallization and preliminary X-ray diffraction analysis of human IL-22 bound to its soluble decoy receptor IL-22BP". Acta Crystallographica. Section F, Structural Biology and Crystallization Communications. 65 (Pt 2): 102–104. doi:10.1107/S1744309108042309. PMC 2635854. PMID 19193995.
  6. ^ Jones BC, Logsdon NJ, Walter MR (September 2008). "Structure of IL-22 bound to its high-affinity IL-22R1 chain". Structure. 16 (9): 1333–1344. doi:10.1016/j.str.2008.06.005. PMC 2637415. PMID 18599299.
  7. ^ de Moura PR, Watanabe L, Bleicher L, Colau D, Dumoutier L, Lemaire MM, et al. (April 2009). "Crystal structure of a soluble decoy receptor IL-22BP bound to interleukin-22". FEBS Letters. 583 (7): 1072–1077. doi:10.1016/j.febslet.2009.03.006. PMID 19285080. S2CID 24846059.
  8. ^ a b c d Martin JC, Bériou G, Heslan M, Chauvin C, Utriainen L, Aumeunier A, et al. (January 2014). "Interleukin-22 binding protein (IL-22BP) is constitutively expressed by a subset of conventional dendritic cells and is strongly induced by retinoic acid". Mucosal Immunology. 7 (1): 101–113. doi:10.1038/mi.2013.28. PMC 4291114. PMID 23653115.
  9. ^ Guendel F, Kofoed-Branzk M, Gronke K, Tizian C, Witkowski M, Cheng HW, et al. (November 2020). "Group 3 Innate Lymphoid Cells Program a Distinct Subset of IL-22BP-Producing Dendritic Cells Demarcating Solitary Intestinal Lymphoid Tissues". Immunity. 53 (5): 1015–1032.e8. doi:10.1016/j.immuni.2020.10.012. PMID 33207209. S2CID 227066350.
  10. ^ Martin JC, Bériou G, Heslan M, Bossard C, Jarry A, Abidi A, et al. (March 2016). "IL-22BP is produced by eosinophils in human gut and blocks IL-22 protective actions during colitis". Mucosal Immunology. 9 (2): 539–549. doi:10.1038/mi.2015.83. PMID 26329427. S2CID 205198781.
  11. ^ a b c Pelczar P, Witkowski M, Perez LG, Kempski J, Hammel AG, Brockmann L, et al. (October 2016). "A pathogenic role for T cell-derived IL-22BP in inflammatory bowel disease". Science. 354 (6310): 358–362. Bibcode:2016Sci...354..358P. doi:10.1126/science.aah5903. PMID 27846573. S2CID 38875063.
  12. ^ a b Fukaya T, Fukui T, Uto T, Takagi H, Nasu J, Miyanaga N, et al. (2018-06-21). "Pivotal Role of IL-22 Binding Protein in the Epithelial Autoregulation of Interleukin-22 Signaling in the Control of Skin Inflammation". Frontiers in Immunology. 9: 1418. doi:10.3389/fimmu.2018.01418. PMC 6021537. PMID 29977242.
  13. ^ Jinnohara T, Kanaya T, Hase K, Sakakibara S, Kato T, Tachibana N, et al. (June 2017). "IL-22BP dictates characteristics of Peyer's patch follicle-associated epithelium for antigen uptake". The Journal of Experimental Medicine. 214 (6): 1607–1618. doi:10.1084/jem.20160770. PMC 5460992. PMID 28512157.
  14. ^ Kempski J, Giannou AD, Riecken K, Zhao L, Steglich B, Lücke J, et al. (October 2020). "IL22BP Mediates the Antitumor Effects of Lymphotoxin Against Colorectal Tumors in Mice and Humans". Gastroenterology. 159 (4): 1417–1430.e3. doi:10.1053/j.gastro.2020.06.033. PMC 7607422. PMID 32585307.
  15. ^ Besnard AG, Sabat R, Dumoutier L, Renauld JC, Willart M, Lambrecht B, et al. (May 2011). "Dual Role of IL-22 in allergic airway inflammation and its cross-talk with IL-17A". American Journal of Respiratory and Critical Care Medicine. 183 (9): 1153–1163. doi:10.1164/rccm.201008-1383OC. PMID 21297073.
  16. ^ Lindahl H, Guerreiro-Cacais AO, Bedri SK, Linnerbauer M, Lindén M, Abdelmagid N, et al. (August 2019). "IL-22 Binding Protein Promotes the Disease Process in Multiple Sclerosis". Journal of Immunology. 203 (4): 888–898. doi:10.4049/jimmunol.1900400. PMID 31292217. S2CID 195879373.
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