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Cytokine receptor








Cytokine receptor


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Key steps of the JAK-STAT pathway for type 1 and 2 cytokine receptors




Signal transduction. (Cytokine receptor at center left.)


Cytokine receptors are receptors that bind cytokines[1].


In recent years, the cytokine receptors have come to demand the attention of more investigators than cytokines themselves, partly because of their remarkable characteristics, and partly because a deficiency of cytokine receptors has now been directly linked to certain debilitating immunodeficiency states. In this regard, and also because the redundancy and pleiotropy of cytokines are a consequence of their homologous receptors, many authorities are now of the opinion that a classification of cytokine receptors would be more clinically and experimentally useful.




Contents





  • 1 Classification


  • 2 Comparison


  • 3 Solubility


  • 4 See also


  • 5 References


  • 6 External links




Classification[edit]


A classification of cytokine receptors based on their three-dimensional structure has been attempted. (Such a classification, though seemingly cumbersome, provides several unique perspectives for attractive pharmacotherapeutic targets.)



  • Type I cytokine receptors, whose members have certain conserved motifs in their extracellular amino-acid domain. The IL-2 receptor belongs to this chain, whose γ-chain (common to several other cytokines) deficiency is directly responsible for the x-linked form of Severe Combined Immunodeficiency (X-SCID).


  • Type II cytokine receptors, whose members are receptors mainly for interferons.


  • Immunoglobulin (Ig) superfamily, which are ubiquitously present throughout several cells and tissues of the vertebrate body


  • Tumor necrosis factor receptor family, whose members share a cysteine-rich common extracellular binding domain, and includes several other non-cytokine ligands like receptors, CD40, CD27 and CD30, besides the ligands on which the family is named (TNF).


  • Chemokine receptors, two of which acting as binding proteins for HIV (CXCR4 and CCR5). They are G protein coupled receptors.

  • TGF beta receptors


Comparison[edit]

























TypeExamplesStructureMechanism

type I cytokine receptor

  • Type 1 interleukin receptors

  • Erythropoietin receptor

  • GM-CSF receptor

  • G-CSF receptor

  • growth hormone receptor

  • prolactin receptor

  • Oncostatin M receptor

  • Leukemia inhibitory factor receptor

Certain conserved motifs in their extracellular amino-acid domain. Connected to Janus kinase (JAK) family of tyrosine kinases
JAK phosphorylate and activate downstream proteins involved in their signal transduction pathways

type II cytokine receptor

  • Type II interleukin receptors

  • interferon-alpha/beta receptor

  • interferon-gamma receptor

Many members of the immunoglobulin superfamily

  • Interleukin-1 receptor

  • CSF1

  • C-kit receptor

  • Interleukin-18 receptor

Share structural homology with immunoglobulins (antibodies), cell adhesion molecules, and even some cytokines.

Tumor necrosis factor receptor family

  • CD27

  • CD30

  • CD40

  • CD120

  • Lymphotoxin beta receptor


cysteine-rich common extracellular binding domain

chemokine receptors

  • Interleukin-8 receptor

  • CCR1

  • CXCR4

  • MCAF receptor

  • NAP-2 receptor


Seven transmembrane helix[2]

G protein-coupled

TGF beta receptors

  • TGF beta receptor 1

  • TGF beta receptor 2



Solubility[edit]


Cytokine receptors may be both membrane-bound and soluble. Soluble cytokine receptors are extremely common regulators of cytokine function. Soluble cytokine receptors typically consist of the extracellular portions of membrane-bound receptors. .[3]



See also[edit]


  • STAT protein


References[edit]




  1. ^ Brooks, Andrew J.; Dehkhoda, Farhad; Kragelund, Birthe B. (2017). "Cytokine Receptors". Principles of Endocrinology and Hormone Action. Springer International Publishing. pp. 1–29. ISBN 9783319273181..mw-parser-output cite.citationfont-style:inherit.mw-parser-output qquotes:"""""""'""'".mw-parser-output code.cs1-codecolor:inherit;background:inherit;border:inherit;padding:inherit.mw-parser-output .cs1-lock-free abackground:url("//upload.wikimedia.org/wikipedia/commons/thumb/6/65/Lock-green.svg/9px-Lock-green.svg.png")no-repeat;background-position:right .1em center.mw-parser-output .cs1-lock-limited a,.mw-parser-output .cs1-lock-registration abackground:url("//upload.wikimedia.org/wikipedia/commons/thumb/d/d6/Lock-gray-alt-2.svg/9px-Lock-gray-alt-2.svg.png")no-repeat;background-position:right .1em center.mw-parser-output .cs1-lock-subscription abackground:url("//upload.wikimedia.org/wikipedia/commons/thumb/a/aa/Lock-red-alt-2.svg/9px-Lock-red-alt-2.svg.png")no-repeat;background-position:right .1em center.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registrationcolor:#555.mw-parser-output .cs1-subscription span,.mw-parser-output .cs1-registration spanborder-bottom:1px dotted;cursor:help.mw-parser-output .cs1-hidden-errordisplay:none;font-size:100%.mw-parser-output .cs1-visible-errorfont-size:100%.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration,.mw-parser-output .cs1-formatfont-size:95%.mw-parser-output .cs1-kern-left,.mw-parser-output .cs1-kern-wl-leftpadding-left:0.2em.mw-parser-output .cs1-kern-right,.mw-parser-output .cs1-kern-wl-rightpadding-right:0.2em


  2. ^ Arimont A, Sun S, Smit MJ, Leurs R, de Esch IJ, de Graaf C (2017). "Structural Analysis of Chemokine Receptor-Ligand Interactions". J Med Chem. doi:10.1021/acs.jmedchem.6b01309. PMID 28165741.


  3. ^ Heaney ML1, Golde DW (1998). "Soluble receptors in human disease". Journal of Leukocyte Biology. 64 (2): 135–146. PMID 9715251.




External links[edit]



  • Cytokine-cytokine receptor interaction map from KEGG


  • Cytokine+receptors at the US National Library of Medicine Medical Subject Headings (MeSH)










Retrieved from "https://en.wikipedia.org/w/index.php?title=Cytokine_receptor&oldid=852248126"





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