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Cytokine receptor

From Wikipedia, the free encyclopedia
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 to cytokines.[1] The binding of cytokines to receptors allows the cell that houses the receptor to be able to receive the signals of another cell. These receptors can be found on the surface of cells that allows them to communicate with other cells that transmit their signals [2]This interaction between cells can involve genetic output, cell cycle changes and other signal transduction responses. Cytokine Receptors play a crucial role in Immunological response.

In recent years,[when?] the cytokine receptors have come to demand the attention of more investigators than cytokines themselves, partly because of their notable 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.

Classification

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Some cytokine receptors have complex structures, with many of them being multi-chain receptors. This is because a cytokine receptor's structure determines its function, and which cytokines will be specific for that receptor. Because of this, 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.)

Comparison

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Type Examples Structure Mechanism
type I cytokine receptor Certain conserved motifs in their extracellular amino-acid domain. Connected to Janus kinase (JAK) family of tyrosine kinases. Many have a FN-III superfamily domain and an immunoglobulin-like fold. JAK phosphorylate and activate downstream proteins involved in their signal transduction pathways
type II cytokine receptor
Many members of the immunoglobulin superfamily Share structural homology with immunoglobulins (antibodies), cell adhesion molecules, and even some cytokine. Includes with the two classes above.
Tumor necrosis factor receptor family cysteine-rich common extracellular binding domain
chemokine receptors Seven transmembrane helix, rhodopsin-like receptor[3] G protein-coupled
TGF-beta receptor family Serine/threonine kinase receptors Dimeric TGFBR2 binds to TGFB and phosphorylates TGFBR1, which phosphorylates the SMADs. See TGF beta signaling pathway.

Solubility

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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. .[4]

Pharmacotherapeutic applications

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Cytokines and their receptors have a major part in the process of the human body's defense systems, Haematopoiesis, and the proliferation of immune cells.[5] Because of this, many scientists have recognized the potential utilizations that cytokine receptors can have for pharmaceutical treatments. Although cytokine receptors have been studied and documented for decades, there are still ongoing studies that are discovering new functions that pertain to immunology and pharmaceutical applications.

Among these applications is the involvement in cytokines and cytokine receptors in treating immune-mediated inflammatory diseases. These diseases occur when cytokines and cytokine receptors are dysregulated, leading to damage to the tissues and unregulated inflammation in the body. To combat these types of diseases, scientists have developed multiple cytokine receptor-targeting treatments. These newly developed treatments can combat several inflammatory and immune diseases, including rheumatoid arthritis, asthma and psoriasis.[6]

Interleukin-6 structure

One of the cytokines involved in the treatment of immune-mediated inflammatory diseases is interleukin-6 receptor. Dysregulation of this receptor occurs when there is a constant increase of the IL-6 cytokine, causing an increase in binding to the its receptor, which promotes inflammation. An influx of binding to the IL-6 receptor can cause inflammation to occur rapidly by activating B cells to produce autoantibodies and over-activating fibroblasts, leading to increased tissue inflammation. This dysregulation can also contribute to Regulatory T cell inhibition, causing inflammation in the body to lack regulation.

To treat diseases that involve the dysregulation of cytokines, a number of treatments are being used and studied. A common method of treating immune-mediated inflammatory diseases is to give monoclonal antibodies that are specific for the IL-6 receptor. Introducing this , type of antibody allows it to bind to the IL-6 receptor, which prevents the binding of IL-6 and its dysregulation of the receptor.

Because of the nature of cytokine's pleiotropy, this introduces potential obstacles to utilizing cytokines and cytokine receptors in pharmaceutical and clinical applications.[7] This is because the ability for cytokines to be able to interact with multiple cell types makes it difficult to utilize their characteristics in a clinical setting.

Erythropoietin is sent by the kidneys to stimulate red blood cell production in the bone marrow

Since cytokine receptors play a role in haematopoiesis, cytokine receptors have also been a common topic to study in the treatment of hematopoietic disorders such as anemia. A major cytokine and cytokine receptor in the process of haematopoiesis is erythropoietin and the erythropoietin receptor. Both have important roles in activating and maintaining red blood cell production. Scientists have studied the uses of stimulating erythropoietin and the erythropoietin receptor for the production of red blood cells in diseases such as kidney disease or certain types of anemia.

See also

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References

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  1. ^ Brooks, Andrew J.; Dehkhoda, Farhad; Kragelund, Birthe B. (2017). "Cytokine Receptors". Principles of Endocrinology and Hormone Action. Springer International Publishing. pp. 1–29. doi:10.1007/978-3-319-27318-1_8-2. ISBN 9783319273181.
  2. ^ Bagley, Christopher J.; Woodcock, Joanna M.; Stomski, Frank C.; Lopez, Angel F. (1997-03-01). "The Structural and Functional Basis of Cytokine Receptor Activation: Lessons From the Common β Subunit of the Granulocyte-Macrophage Colony-Stimulating Factor, Interleukin-3 (IL-3), and IL-5 Receptors". Blood. 89 (5): 1471–1482. doi:10.1182/blood.V89.5.1471. ISSN 0006-4971.
  3. ^ 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. 60 (12): 4735–4779. doi:10.1021/acs.jmedchem.6b01309. PMC 5483895. PMID 28165741.
  4. ^ Heaney, ML; Golde, DW (1998). "Soluble receptors in human disease". Journal of Leukocyte Biology. 64 (2): 135–146. doi:10.1002/jlb.64.2.135. PMID 9715251. S2CID 34021597.[permanent dead link]
  5. ^ Foster, Don; Parrish-Novak, Julia; Fox, Brian; Xu, Wenfeng (February 2004). "Cytokine–receptor pairing: accelerating discovery of cytokine function". Nature Reviews Drug Discovery. 3 (2): 160–170. doi:10.1038/nrd1305. ISSN 1474-1784. PMID 15040579.
  6. ^ Takeuchi, Tsutomu (2022-12-01). "Cytokines and cytokine receptors as targets of immune-mediated inflammatory diseases—RA as a role model". Inflammation and Regeneration. 42 (1) 35. doi:10.1186/s41232-022-00221-x. ISSN 1880-8190. PMC 9713106. PMID 36451227.
  7. ^ Saxton, Robert A.; Glassman, Caleb R.; Garcia, K. Christopher (January 2023). "Emerging principles of cytokine pharmacology and therapeutics". Nature Reviews Drug Discovery. 22 (1): 21–37. doi:10.1038/s41573-022-00557-6. ISSN 1474-1776. PMC 10292932. PMID 36131080.
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