The chemokine CXC4 and CC2 receptors form homo- and heterooligomers that can engage their signaling G-protein effectors and βarrestin

FASEB J. 2014 Oct;28(10):4509-23. doi: 10.1096/fj.13-242446. Epub 2014 Jul 22.


G-protein-coupled receptors have been shown to assemble at least as dimers early in the biosynthetic path, but some evidence suggests that they can also form larger oligomeric complexes. Using the human chemokine receptors CXCR4 and CCR2 as models, we directly probed the existence of higher order homo- and heterooligomers in human embryonic kidney cells. Combining bimolecular fluorescence and luminescence complementation (BiFC, BiLC) with bioluminescence resonance energy transfer (BRET) assays, we show that CXCR4 and CCR2 can assemble as homo- and heterooligomers, forming at least tetramers. Selective activation of CCR2 with the human monocyte chemotactic protein 1 (MCP-1) resulted in trans-conformational rearrangement of the CXCR4 dimer with an EC50 of 19.9 nM, compatible with a CCR2 action. Moreover, MCP-1 promoted the engagement of Gαi1, Gα13, Gαz, and βarrestin2 to the heterooligomer, resulting in calcium signaling that was synergistically potentiated on coactivation of CCR2 and CXCR4, demonstrating that complexes larger than dimers reach the cell surface as functional units. A mutation of CXCR4 (N119K), which prevents Gi activation, also affects the CCR2-promoted engagement of Gαi1 and βarrestin2 by the heterooligomer, supporting the occurrence of transprotomer regulation. Together, the results demonstrate that homo- and heteromultimeric CXCR4 and CCR2 can form functional signaling complexes that have unique properties.

Keywords: GPCR; allosteric regulation; complex formation; protein complementation assays; resonance energy transfer; transactivation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arrestins / metabolism*
  • Chemokine CCL2 / metabolism*
  • GTP-Binding Protein alpha Subunits / metabolism*
  • HEK293 Cells
  • Humans
  • Protein Binding
  • Protein Multimerization
  • Receptors, CCR2 / metabolism*
  • Receptors, CXCR4 / genetics
  • Receptors, CXCR4 / metabolism*
  • Signal Transduction*
  • beta-Arrestins


  • Arrestins
  • CCL2 protein, human
  • CCR2 protein, human
  • CXCR4 protein, human
  • Chemokine CCL2
  • GTP-Binding Protein alpha Subunits
  • Receptors, CCR2
  • Receptors, CXCR4
  • beta-Arrestins