Histamine H4 receptor

HRH4
Identifiers
AliasesHRH4, AXOR35, BG26, GPCR105, GPRv53, H4, H4R, HH4R, histamine receptor H4
External IDsOMIM: 606792 MGI: 2429635 HomoloGene: 11002 GeneCards: HRH4
Gene location (Human)
Chr.Chromosome 18 (human)[1]
BandNo data availableStart24,460,629 bp[1]
End24,479,957 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

59340

225192

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: 13.01 – 13.02 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

The histamine H4 receptor is, like the other three histamine receptors, a member of the G protein-coupled receptor superfamily.[5][6][7]

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.[8] It is also expressed in the colon, liver, lung, small intestine, spleen, testes, thymus, tonsils, and trachea.[9] It was also found that H4R 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 polymerisation and eventually chemotaxis.

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[12] was built by homology modelling based on the crystal structure of bovine rhodopsin.[13] 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.[14]

Recent advancements in GPCR crystallization, in particular the determination of the human histamine H1 receptor in complex with doxepin[15] will likely increase the quality of novel structural H4 receptor models.[16][17]

Ligands

Agonists

Antagonists

Therapeutic potential

By inhibiting the H4 receptor, asthma and allergy may be treated.[18]

The highly selective histamine H4 antagonist VUF-6002 is orally active and inhibits the activity of both mast cells and eosinophils in vivo,[19] and has antiinflammatory and antihyperalgesic effects.[20]

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000134489 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000037346 - Ensembl, May 2017
  3. ↑ "Human PubMed Reference:".
  4. ↑ "Mouse PubMed Reference:".
  5. ↑ Oda T, Morikawa N, Saito Y, Masuho Y, Matsumoto S (2000). "Molecular cloning and characterization of a novel type of histamine receptor preferentially expressed in leukocytes". J. Biol. Chem. 275 (47): 36781–6. PMID 10973974. doi:10.1074/jbc.M006480200.
  6. ↑ Nakamura T, Itadani H, Hidaka Y, Ohta M, Tanaka K (2000). "Molecular cloning and characterization of a new human histamine receptor, HH4R". Biochem. Biophys. Res. Commun. 279 (2): 615–20. PMID 11118334. doi:10.1006/bbrc.2000.4008.
  7. ↑ Nguyen T, Shapiro DA, George SR, Setola V, Lee DK, Cheng R, Rauser L, Lee SP, Lynch KR, Roth BL, O'Dowd BF (2001). "Discovery of a novel member of the histamine receptor family" (abstract). Mol. Pharmacol. 59 (3): 427–33. PMID 11179435.
  8. ↑ Takeshita K, Bacon KB, Gantner F (2004). "Critical role of L-selectin and histamine H4 receptor in zymosan-induced neutrophil recruitment from the bone marrow: comparison with carrageenan". J. Pharmacol. Exp. Ther. 310 (1): 272–80. PMID 14996947. doi:10.1124/jpet.103.063776.
  9. ↑ Bioreagents.com: Histamine H4 Receptor
  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: http://dx.doi.org/10.1111/bjd.14995.
  11. ↑ Hofstra CL, Desai PJ, Thurmond RL, Fung-Leung WP (2003). "Histamine H4 receptor mediates chemotaxis and calcium mobilization of mast cells". J. Pharmacol. Exp. Ther. 305 (3): 1212–21. PMID 12626656. doi:10.1124/jpet.102.046581.
  12. ↑ Shin N, Coates E, Murgolo NJ, Morse KL, Bayne M, Strader CD, Monsma FJ (July 2002). "Molecular modeling and site-specific mutagenesis of the histamine-binding site of the histamine H4 receptor". Mol. Pharmacol. 62 (1): 38–47. PMID 12065753. doi:10.1124/mol.62.1.38.
  13. ↑ Palczewski K, Kumasaka T, Hori T, Behnke CA, Motoshima H, Fox BA, Le Trong I, Teller DC, Okada T, Stenkamp RE, Yamamoto M, Miyano M (August 2000). "Crystal structure of rhodopsin: A G protein-coupled receptor". Science. 289 (5480): 739–45. PMID 10926528. doi:10.1126/science.289.5480.739.
  14. ↑ Kiss R, Kiss B, Könczöl A, Szalai F, Jelinek I, László V, Noszál B, Falus A, Keseru GM (June 2008). "Discovery of novel human histamine H4 receptor ligands by large-scale structure-based virtual screening". J. Med. Chem. 51 (11): 3145–53. PMID 18459760. doi:10.1021/jm7014777. Lay summary – blog.mcule.com.
  15. ↑ Shimamura T, Shiroishi M, Weyand S, Tsujimoto H, Winter G, Katritch V, Abagyan R, Cherezov V, Liu W, Han GW, Kobayashi T, Stevens RC, Iwata S (June 2011). "Structure of the human histamine H(1) receptor complex with doxepin". Nature. 475 (7354). PMC 3131495 Freely accessible. PMID 21697825. doi:10.1038/nature10236.
  16. ↑ Schultes S, Nijmeijer S, Engelhardt H, Kooistra AJ, Vischer HF, de Esch IJ, Haaksma EJ, Leurs R, de Graaf C (2013). "Mapping histamine H4 receptor-ligand binding modes". MedChemComm. 4: 193–204. doi:10.1039/C2MD20212C.
  17. ↑ Nijmeijer S, Engelhardt H, Schultes S, van de Stolpe AC, Lusink V, de Graaf C, Wijtmans M, Haaksma EE, de Esch IJ, Stachurski K, Vischer HF, Leurs R (2013). "Design and pharmacological characterization of VUF14480, a covalent partial agonist that interacts with cysteine 98(3.36) of the human histamine H₄ receptor.". Br J Pharmacol. 170 (1): 89–100. PMID 23347159. doi:10.1111/bph.12113.
  18. ↑ InterPro: IPR008102 Histamine H4 receptor
  19. ↑ Varga, C; Horvath, K; Berko, A; Thurmond, RL; Dunford, PJ; Whittle, BJ. (2005). "Inhibitory effects of histamine H4 receptor antagonists on experimental colitis in the rat". European Journal of Pharmacology. 522 (1-3): 130–8. PMID 16213481. doi:10.1016/j.ejphar.2005.08.045.
  20. ↑ Coruzzi, G; Adami, M; Guaita, E; de Esch, IJ; Leurs, R. (2007). "Antiinflammatory and antinociceptive effects of the selective histamine H4-receptor antagonists JNJ7777120 and VUF6002 in a rat model of carrageenan-induced acute inflammation". European Journal of Pharmacology. 563 (1-3): 240–4. PMID 17382315. doi:10.1016/j.ejphar.2007.02.026.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.