CLEC6A
| CLEC6A | |||||||||||||||||||||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Aliases | CLEC6A, CLEC4N, CLECSF10, C-type lectin domain family 6 member A, dectin-2, C-type lectin domain containing 6A, hDECTIN-2 | ||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | OMIM: 613579; MGI: 1861231; HomoloGene: 84615; GeneCards: CLEC6A; OMA:CLEC6A - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
| |||||||||||||||||||||||||||||||||||||||||||||||||||
| |||||||||||||||||||||||||||||||||||||||||||||||||||
| |||||||||||||||||||||||||||||||||||||||||||||||||||
| |||||||||||||||||||||||||||||||||||||||||||||||||||
| |||||||||||||||||||||||||||||||||||||||||||||||||||
| Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
| |||||||||||||||||||||||||||||||||||||||||||||||||||
Dectin-2 or C-type lectin domain containing 6A is a protein that in humans is encoded by the CLEC6A gene.[5] Dectin-2 is a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. The encoded protein is a type II transmembrane protein with an extracellular carbohydrate recognition domain. It functions as a pattern recognition receptor recognizing α-mannans and as such plays an important role in innate immune response to fungi. Expression is found on macrophages and dendritic cells. It can also be found at low levels in Langerhans cells and peripheral blood monocytes, where expression levels could be increased upon induction of inflammation.[6][7]
Dectin-2 genes are located in the telomeric region of the natural killer gene cluster on mouse chromosome 6 and human chromosome 12. The dectin-2 cluster is composed of genes encoding dectin-2, DCIR, DCAR, BDCA-2, Mincle and Clecsf8, which are the members of the group II C-type lectin family.[7]
Structure
[edit]Dectin-2 is a glycosylated type II transmembrane protein which is encoded by six exons. It consists of a single C-type lectin (carbohydrate recognition domain, CRD) domain in its extracellular region, a stalk region, a transmembrane region and a cytoplasmic domain. Its CRD domain contains a glutamic acid-proline-asparagine (EPN) motif, which is Ca2+ dependent.[6] The cytoplasmic domain is generally short. Unlike dectin-1, it has no known signaling motif in its cytoplasmic region. Instead, upon ligand binding, dectin-2 transduces signal via association with the ITAM-containing Fc receptor γ chain.[6][7]
Signaling
[edit]Dectin-2 is a member of C-type lectin receptor family, which is a group of pattern recognition receptors involved in antifungal immunity, homeostasis and induction of immune response to pathogens. Its carbohydrate recognition domain is capable of binding α-mannans in fungal cell walls. Upon ligand binding, dectin-2 transduces the signal via an ITAM-bearing adaptor protein FcγR. This results in recruitment of Syk and downstream activation of so-called CBM (CARD9-BCL10-MALT1) signalling complex, leading to NFκB activation and resulting in production of cytokines, including IL-6, IL-23 and IL-1β.[6][7]
Aforementioned signaling pathway leads to induction of phagocytosis and production of inflammatory mediators, such as cytokines and chemokines, induction of both innate and adaptive immunity and overall antimicrobial response.[6][7][8]
Signaling induced by dectin-2 activation also augments IL-17RC expression in neutrophils, and is involved in IL-17A and IL-17RC autocrine feedback loop, which is important for ROS production and subsequent elimination of fungal pathogen.[8][5]
Dectin-2 has also been reported to be involved in activation of MAPK signaling.[8]
E3 ubiquitin ligase CBLB has been described as negative regulator of dectin-2.[9]
Ligands
[edit]Dectin-2 is known to recognize α-mannans, which are an important component of fungal cell wall. It has also been reported to recognize glycoproteins rich in O-mannobiose residues.[5]
Functions
[edit]Anti-fungal immunity
[edit]Dectin-2 signaling is an essential component of host defense against fungal infections. It has been observed that dectin-2 preferentially induces the Th17 response, which is essential for effective host protection and elimination of fungal pathogens. Cytokines produced after dectin-2 activation include IL-6, IL-23 and IL-1β, all of which are typical for Th17 response. Dectin-2 can also induce production of IL-12, which stimulates Th1 lymphocytes to produce IFN-γ. This in turn leads to activation of macrophages and contributes to fungal eradication.[6][10]
Anti-inflammatory cytokines such as IL-2 and IL-10 can also be induced by dectin-2.[6]
Most abundantly studied is the role of dectin-2 in Candida albicans infections, and it has been observed that this receptor is important for effective host defense and C. albicans clearance. Mice lacking dectin-2 demonstrated greatly increased susceptibility to C. albicans infections, supporting that this receptor is essential for the induction of effective immune response. The functions of dectin-2 appear to differ between the yeast and hyphal forms of C. albicans. Possibly due to different cell wall ligands, as these two forms are known to slightly differ in terms of cell wall organization. Dectin-2 could possibly be able to distinguish between the two morphological forms of C. albicans.[10]
Dectin-2 has also been shown to interact with Dectin-3, witch which it can form a heterodimer in order to mediate the immune defense against Candida albicans.[6]
While Dectin-2 is known to mediate immune response to Candida albicans, it recognizes a variety of different pathogens, which include Candida glabrata, Cryptococcus neoformans, Aspergillus fumigatus, Saccharomyces cerevisiae, Mycobacterium tuberculosis, Paracoccidioides brasiliensis and Histoplasma capsulatum among other species.[6][10]
Other functions
[edit]Dectin-2 has also been linked to allergic responses. It is reportedly able to recognize the house dust mite (arachnids known to cause allergy), and subsequently induce cysteinyl leukotriene production. These mediators, along with cytokines such as IL-33, are essential for the initiation of airway inflammation and for induction of Th2 response.[7][5]
References
[edit]- ^ a b c GRCh38: Ensembl release 89: ENSG00000205846 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000023349 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ a b c d Dambuza IM, Brown GD (February 2015). "C-type lectins in immunity: recent developments". Current Opinion in Immunology. 32: 21–27. doi:10.1016/j.coi.2014.12.002. PMC 4589735. PMID 25553393.
- ^ a b c d e f g h i Saijo S, Iwakura Y (August 2011). "Dectin-1 and Dectin-2 in innate immunity against fungi". International Immunology. 23 (8): 467–472. doi:10.1093/intimm/dxr046. PMID 21677049.
- ^ a b c d e f Graham LM, Brown GD (October 2009). "The Dectin-2 family of C-type lectins in immunity and homeostasis". Cytokine. 48 (1–2): 148–155. doi:10.1016/j.cyto.2009.07.010. PMC 2756403. PMID 19665392.
- ^ a b c Goyal S, Castrillón-Betancur JC, Klaile E, Slevogt H (2018). "The Interaction of Human Pathogenic Fungi With C-Type Lectin Receptors". Frontiers in Immunology. 9: 1261. doi:10.3389/fimmu.2018.01261. PMC 5994417. PMID 29915598.
- ^ Borriello F, Zanoni I, Granucci F (March 2020). "Cellular and molecular mechanisms of antifungal innate immunity at epithelial barriers: The role of C-type lectin receptors". European Journal of Immunology. 50 (3): 317–325. doi:10.1002/eji.201848054. PMC 10668919. PMID 31986556. S2CID 210933900.
- ^ a b c Kerscher B, Willment JA, Brown GD (May 2013). "The Dectin-2 family of C-type lectin-like receptors: an update". International Immunology. 25 (5): 271–277. doi:10.1093/intimm/dxt006. PMC 3631001. PMID 23606632.