Histamine H4 receptor

Source: Wikipedia, the free encyclopedia.
HRH4
Identifiers
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Ensembl

ENSG00000134489

ENSMUSG00000037346

UniProt

Q9H3N8

Q91ZY2

RefSeq (mRNA)

NM_001143828
NM_001160166
NM_021624

NM_153087

RefSeq (protein)

NP_001137300
NP_001153638
NP_067637

NP_694727

Location (UCSC)Chr 18: 24.46 – 24.48 MbChr 18: 13.14 – 13.16 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

The histamine H4 receptor, like the other three

histamine receptors, is a member of the G protein-coupled receptor superfamily that in humans is encoded by the HRH4 gene.[5][6][7]

Discovery

Unlike the histamine receptors discovered earlier, H4 was found in 2000 through a search of the human genomic DNA data base.[8]

Tissue distribution

H4 is highly expressed in bone marrow and white blood cells and regulates neutrophil release from bone marrow and subsequent infiltration in the zymosan-induced pleurisy mouse model.[9] It was also found that H4 receptor exhibits a uniform expression pattern in the human oral epithelium.[10]

Function

The Histamine H4 receptor has been shown to be involved in mediating

eosinophil shape change and mast cell chemotaxis.[11] This occurs via the βγ subunit acting at phospholipase C to cause actin polymerization and eventually chemotaxis.[11]

The histamine H4 receptor has been identified as a vital regulator of the immune system, involved in eosinophil migration, mast cell recruitment, dendritic cell activation, and T cell differentiation. The discovery of this receptor has brought it to increasing attention for its therapeutic use in inflammatory diseases such as allergy, asthma, chronic itch, and autoimmune diseases.[12]

Structure

The 3D structure of the H4 receptor has not been solved yet due to the difficulties of GPCR crystallization. Some attempts have been made to develop structural models of the H4 receptor for different purposes. The first H4 receptor model[13] was built by homology modelling based on the crystal structure of bovine rhodopsin.[14] This model was used for the interpretation of site-directed mutagenesis data, which revealed the crucial importance of Asp94 (3.32) and Glu182 (5.46) residues in ligand binding and receptor activation.

A second rhodopsin based structural model of the H4 receptor was successfully used for the identification of novel H4 ligands.[15]

Recent advancements in GPCR crystallization, in particular the determination of the human histamine H1 receptor in complex with doxepin[16] will likely increase the quality of novel structural H4 receptor models.[17][18]

Ligands

Although the effectiveness of H4 receptor ligands has been studied in animal models and human biological samples, further research is needed to understand genetic polymorphisms and interspecies differences in their actions and pharmacological characteristics.[12]

Agonists

Antagonists

Therapeutic potential

The available data support the H4 receptor as a promising new drug target for modulating histamine-mediated immune signaling and offer optimistic prospects for developing new therapies for inflammatory diseases.[12]

H4 receptor antagonists could be used to treat asthma and allergies.[19]

The highly selective histamine H4 antagonist VUF-6002 is orally active and inhibits the activity of both mast cells and eosinophils in vivo,[20] and has anti-inflammatory and antihyperalgesic effects.[21]

See also

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000134489 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000037346 – Ensembl, 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. PMID 10973974
    .
  6. PMID 11118334
    .
  7. PMID 11179435
    .
  8. PMID 10973974
    .
  9. S2CID 6698467
    .
  10. ^ Salem A, Rozov S, Al-Samadi A, et al. Histamine metabolism and transport are deranged in human keratinocytes in oral lichen planus. Br J Dermatol. 2016. Available at: https://dx.doi.org/10.1111/bjd.14995.
  11. ^
    S2CID 14932773
    .
  12. ^
    PMID 19309354
    .
  13. S2CID 16628657
    .
  14. PMID 10926528
    .
  15. PMID 18459760
    .
  16. PMID 21697825
    .
  17. doi:10.1039/C2MD20212C
    .
  18. PMID 23347159
    .
  19. ^ InterPro: IPR008102 Histamine H4 receptor
  20. PMID 16213481
    .
  21. PMID 17382315
    .

External links
Retrieved from "https://en.wikipedia.org/w/index.php?title=Histamine_H4_receptor&oldid=1191988756"