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CD23

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(Redirected from FCER2) Low-affinity" receptor for IgE
FCER2
Available structures
PDBOrtholog search: PDBe RCSB
List of PDB id codes

4KI1, 1T8C, 1T8D, 2H2R, 2H2T, 4EZM, 4G96, 4G9A, 4GI0, 4GJ0, 4GJX, 4GK1, 4GKO, 4J6J, 4J6K, 4J6L, 4J6M, 4J6N, 4J6P, 4J6Q

Identifiers
AliasesFCER2, BLAST-2, CD23, CD23A, CLEC4J, FCE2, IGEBF, Fc fragment of IgE receptor II, FCErII, Fc epsilon receptor II
External IDsOMIM: 151445; MGI: 95497; HomoloGene: 1517; GeneCards: FCER2; OMA:FCER2 - orthologs
Gene location (Human)
Chromosome 19 (human)
Chr.Chromosome 19 (human)
Chromosome 19 (human)Genomic location for FCER2Genomic location for FCER2
Band19p13.2Start7,688,758 bp
End7,702,146 bp
Gene location (Mouse)
Chromosome 8 (mouse)
Chr.Chromosome 8 (mouse)
Chromosome 8 (mouse)Genomic location for FCER2Genomic location for FCER2
Band8 A1.1|8 1.92 cMStart3,731,737 bp
End3,744,175 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • testicle

  • granulocyte

  • spleen

  • lymph node

  • appendix

  • blood

  • monocyte

  • mucosa of transverse colon

  • bone marrow cells

  • tonsil
Top expressed in
  • mesenteric lymph nodes

  • spleen

  • blood

  • subcutaneous adipose tissue

  • granulocyte

  • embryo

  • thymus

  • tibiofemoral joint

  • white adipose tissue

  • morula
More reference expression data
BioGPS


More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

2208

14128

Ensembl

ENSG00000104921

ENSMUSG00000005540

UniProt

P06734

P20693

RefSeq (mRNA)

NM_001207019
NM_001220500
NM_002002

NM_001253737
NM_001253739
NM_001253743
NM_001253745
NM_001253746

NM_001253747
NM_013517

RefSeq (protein)

NP_001193948
NP_001207429
NP_001993

NP_001240666
NP_001240668
NP_001240672
NP_001240674
NP_001240675

NP_001240676
NP_038545

Location (UCSC)Chr 19: 7.69 – 7.7 MbChr 8: 3.73 – 3.74 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

CD23, also known as Fc epsilon RII, or FcεRII, is the "low-affinity" receptor for IgE, an antibody isotype involved in allergy and resistance to parasites, and is important in regulation of IgE levels. Unlike many of the antibody receptors, CD23 is a C-type lectin. It is found on mature B cells, activated macrophages, eosinophils, follicular dendritic cells, and platelets.

There are two forms of CD23: CD23a and CD23b. CD23a is present on follicular B cells, whereas CD23b requires IL-4 to be expressed on T-cells, monocytes, Langerhans cells, eosinophils, and macrophages.

Function

CD23 is known to have a role of transportation in antibody feedback regulation. Antigens which enter the blood stream can be captured by antigen specific IgE antibodies. The IgE immune complexes that are formed bind to CD23 molecules on B cells, and are transported to the B cell follicles of the spleen. The antigen is then transferred from CD23+ B cells to CD11c+ antigen presenting cells. The CD11c+ cells in turn present the antigen to CD4+ T cells, which can lead to an enhanced antibody response.

Clinical significance

The allergen responsible in dust mite allergyDer p 1—is known to cleave CD23 from a cell’s surface. As CD23 is soluble, it can move freely and interact with cells in plasma. Recent studies have shown that increased levels of soluble CD23 cause the recruitment of non-sensitised B-cells in the presentation of antigen peptides to allergen-specific B-cells, therefore increasing the production of allergen specific IgE. IgE, in turn, is known to upregulate the cellular expression of CD23 and Fc epsilon RI (high-affinity IgE receptor).

Patterns of CD23 (and CD21) expression by the follicular dendritic cells in follicular lymphoma.

In flow cytometry, CD23 is helpful in the differentiation of chronic lymphocytic leukemia (CD23-positive) from mantle cell lymphoma (CD23-negative). CD23 can also be demonstrated in germinal centre follicular dendritic cells using immunohistochemistry but is minimally expressed by benign germinal center B cells. In contrast to neoplastic mantle cells (which are negative for CD23), the resting cells of physiologic mantle zone express CD23. Paradoxically, Lymphomas arising from the mantle zone are generally negative for CD23, while most B-cell chronic lymphomocytic leukaemias are positive, allowing immunohistochemistry to distinguish these conditions, which otherwise have a similar appearance. Reed – Sternberg cells are usually positive for CD23.

See also

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000104921Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000005540Ensembl, 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. Lichtman AH, Abbas AK (2003). Cellular and molecular immunology. Philadelphia: Saunders. pp. 324–325. ISBN 0-7216-0008-5.
  6. Henningsson F, Ding Z, Dahlin JS, Linkevicius M, Carlsson F, Grönvik KO, Hallgren J, Heyman B (2011). Metzger DW (ed.). "IgE-mediated enhancement of CD4+ T cell responses in mice requires antigen presentation by CD11c+ cells and not by B cells". PLOS ONE. 6 (7): e21760. Bibcode:2011PLoSO...621760H. doi:10.1371/journal.pone.0021760. PMC 3130775. PMID 21765910.
  7. Engeroff P, Vogel M (July 2021). "The role of CD23 in the regulation of allergic responses". Allergy. 76 (7): 1981–1989. doi:10.1111/all.14724. PMC 8359454. PMID 33378583.
  8. Kurshumliu F, Sadiku-Zehri F, Qerimi A, Vela Z, Jashari F, Bytyci S, et al. (2019). "Divergent immunohistochemical expression of CD21 and CD23 by follicular dendritic cells with increasing grade of follicular lymphoma". World J Surg Oncol. 17 (1): 115. doi:10.1186/s12957-019-1659-8. PMC 6610797. PMID 31269981.
    - This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/)
  9. Barna G, Reiniger L, Tátrai P, Kopper L, Matolcsy A (Sep 2008). "The cut-off levels of CD23 expression in the differential diagnosis of MCL and CLL". Hematological Oncology. 26 (3): 167–70. doi:10.1002/hon.855. PMID 18381689. S2CID 20572446.
  10. Cooper K, Leong AS (2003). Manual of diagnostic antibodies for immunohistology. London: Greenwich Medical Media. p. 95. ISBN 1-84110-100-1.

Further reading

External links

  • Human FCER2 genome location and FCER2 gene details page in the UCSC Genome Browser.
  • PDBe-KB provides an overview of all the structure information available in the PDB for Human Low affinity immunoglobulin epsilon Fc receptor


PDB gallery
  • 1t8c: Structure of the C-type lectin domain of CD23 1t8c: Structure of the C-type lectin domain of CD23
  • 1t8d: Structure of the C-type lectin domain of CD23 1t8d: Structure of the C-type lectin domain of CD23
  • 2h2r: Crystal structure of the human CD23 Lectin domain, apo form 2h2r: Crystal structure of the human CD23 Lectin domain, apo form
  • 2h2t: CD23 Lectin domain, Calcium 2+-bound 2h2t: CD23 Lectin domain, Calcium 2+-bound
Proteins: clusters of differentiation (see also list of human clusters of differentiation)
1–50
51–100
101–150
151–200
201–250
251–300
301–350
Cluster of differentiation by lineage
Lymphoid
B cell
T/NK
T cell
NK cell
All
All
Myeloid
CFU-GM/
Myelomonocyte
MEP
CFU-Meg
CFU-E
All (pan-myeloid)
Stem cell
Transmembrane receptors: immunoglobulin superfamily immune receptors
Antibody receptor:
Fc receptor
Epsilon (ε)
Gamma (γ)
Alpha (α)/mu (μ)
Secretory
Antigen receptor
B cells
Antigen receptor
Co-receptor
stimulate:
inhibit:
Accessory molecules
T cells
Ligands
Antigen receptor
Co-receptors
Accessory molecules
Cytokine receptor
Killer-cell IG-like receptors
Leukocyte IG-like receptors
Categories: