© 2010


Structure to Function

  • Simon Yona
  • Martin Stacey
  • Includes evolution of the adhesion-GPCR genes in several species

  • Explores how this proteolytic cleavage was identified as an intrinsic protein modification process in the majority adhesion-GPCRs

  • Describes the expression of adhesion-GPCRs within the male reproductive tract and reviews their potential contribution in reproductive competence


Part of the Advances in Experimental Medicine and Biology book series (AEMB, volume 706)

Table of contents

  1. Front Matter
    Pages i-xxi
  2. Helgi B. Schiöth, Karl J. V. Nordström, Robert Fredriksson
    Pages 1-13
  3. Tobias Langenhan, Andreas P. Russ
    Pages 37-48
  4. Hsi-Hsien Lin, Martin Stacey, Simon Yona, Gin-Wen Chang
    Pages 49-58
  5. John-Paul Silva, Yuri A. Ushkaryov
    Pages 59-75
  6. Natalie Strokes, Xianhua Piao
    Pages 87-97
  7. Gabriela Aust
    Pages 109-120
  8. Simon Yona, Hsi-Hsien Lin, Martin Stacey
    Pages 121-127
  9. Jörg Hamann, Henrike Veninga, Dorien M. de Groot, Lizette Visser, Claudia L. Hofstra, Paul P. Tak et al.
    Pages 128-137
  10. Ian Spendlove, Ruhcha Sutavani
    Pages 138-148
  11. Hsi-Hsien Lin, Martin Stacey, Joan Stein-Streilein, Siamon Gordon
    Pages 149-156
  12. Norikazu Mizuno, Hiroshi Itoh
    Pages 157-166
  13. Daeho Park, Kodi S. Ravichandran
    Pages 167-178
  14. Ben Davies, Christiane Kirchhoff
    Pages 179-188
  15. Back Matter
    Pages 189-199

About this book


Upon completion of the human genome project over 800 G protein-coupled receptor 1 (GPCR) genes, subdivided into five categories, were identified. These receptors sense a diverse array of stimuli, including peptides, ions, lipid analogues, light and odour, in a discriminating fashion. Subsequently, they transduce a signal from the ligand–receptor complex into numerous cellular responses. The importance of GPCRs is further reflected in the fact that they constitute the most common target for therapeutic drugs across a 2 wide range of human disorders. Phylogenetic analysis of GPCRs produced the GRAFS classification system, which subdivides GPCRs into five discrete families: glutamate, rhodopsin, adhesion, frizzled/taste2 and secretin receptors. The adhesion-GPCR family 2 can be further subdivided into eight groups. The field of adhesion-GPCR biology has indeed become large enough to require a volume dedicated solely to this field. The contributors to this book have made a courageous effort to address the key concepts of adhesion-GPCR biology, including the evolution and biochemistry of adhesion-GPCRs; there are extensive discussions on the functional nature of these receptors during development, the immune response and tumourgenesis. Finally, there are chapters dedicated to adhesion-GPCR signalling, an area of intense investigation.


Adhesion Function GPCR Stacey Structure Yona leukocyte tissue

Editors and affiliations

  • Simon Yona
    • 1
  • Martin Stacey
    • 2
  1. 1.Department of ImmunologyThe Weizmann Institute of ScienceRehovotIsrael
  2. 2.Institute of Molecular and Cellular BiologyUniversity of LeedsLeedsUK

About the editors

Simon Yona, PhD, graduated from Kings College, University London with a BSc in Physiology and a MSc in Pharmacology, before completing a PhD with Prof. R.J. Flower FRS and Prof. M. Perretti, at St. Bartholomew’s Hospital, University of London. Following his doctorate Simon took up a Postdoctoral Research position with Prof. S. Gordon FRS, at the Sir William Dunn School of Pathology, University of Oxford, where he investigated the roles and functions of the leukocyte restricted adhesion‑GPCRs. Dr. Yona moved from Oxford to join the group of Prof. S. Jung, at the Weizmann Institute of Science, Rehovot, when he was awarded a Federation of European Biochemical Societies, International Fellowship. Currently he is investigating the developmental profile of mononuclear phagocytes in a number of pathologies. Martin Stacey, DPhil (Oxon), graduated from Hertford College, University of Oxford with an MBiochem before completing a DPhil in the laboratory of Prof. S. Gordon FRS. He continued working at the Sir William Dunn School of Pathology for a number of years where he cloned and characterized leukocyte adhesion‑GPCRs and demonstrated the existence of their cell surface ligands. More recently, Dr. Stacey has been appointed as a Lecturer of Immunology, at the University of Leeds where his laboratory focuses on adhesion‑GPCRs and role of myeloid cells in human disease.

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