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An atypical addition to the chemokine receptor nomenclature: IUPHAR Review 15

Journal

BRITISH JOURNAL OF PHARMACOLOGY
Volume 172, Issue 16, Pages 3945-3949

Publisher

WILEY-BLACKWELL
DOI: 10.1111/bph.13182

Keywords

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Funding

  1. Investissements d'Avenir
  2. INSERM
  3. ERA-Net for Research Programmes on Rare Diseases [E-Rare-013]
  4. Italian Association for Cancer Research
  5. European Commission
  6. Italian Ministry of Education, Universities and Research
  7. Italian Ministry of Health
  8. Division of Intramural Research of the National Institute of Allergy and Infectious Diseases
  9. Medical Research Council [G0802838]
  10. Wellcome Trust
  11. Helmut Horten Foundation
  12. Swiss National Science Foundation
  13. Chief Scientist Office [ETM/67, ETM/276, ETM/115, CZB/4/697] Funding Source: researchfish
  14. Medical Research Council [G0901113, G0802838, MR/M019764/1] Funding Source: researchfish
  15. Wellcome Trust [099251/Z/12/Z] Funding Source: researchfish
  16. MRC [G0802838, G0901113, MR/M019764/1] Funding Source: UKRI

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Chemokines and their receptors are essential regulators of in vivo leukocyte migration and, some years ago, a systematic nomenclature system was developed for the chemokine receptor family. Chemokine receptor biology and biochemistry was recently extensively reviewed. In this review, we also highlighted a new component to the nomenclature system that incorporates receptors previously known as scavenging', or decoy', chemokine receptors on the basis of their lack of classical signalling responses to ligand binding and their general ability to scavenge, or sequester, their cognate chemokine ligands. These molecules are now collectively referred to as atypical chemokine receptors', or ACKRs, and play fundamental roles in regulating in vivo responses to chemokines. This commentary highlights this new addition to the chemokine receptor nomenclature system and provides brief information on the four receptors currently covered by this nomenclature.

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