G protein subtype-specific signaling bias in a series of CCR5 chemokine analogs

Sci Signal. 2018 Oct 16;11(552):eaao6152. doi: 10.1126/scisignal.aao6152.

Abstract

Chemokines and some chemical analogs of chemokines prevent cellular HIV-1 entry when bound to the HIV-1 coreceptors C-C chemokine receptor 5 (CCR5) or C-X-C chemokine receptor 4 (CXCR4), which are G protein-coupled receptors (GPCRs). The ideal HIV-1 entry blocker targeting the coreceptors would display ligand bias and avoid activating G protein-mediated pathways that lead to inflammation. We compared CCR5-dependent activation of second messenger pathways in a single cell line. We studied two endogenous chemokines [RANTES (also known as CCL5) and MIP-1α (also known as CCL3)] and four chemokine analogs of RANTES (5P12-, 5P14-, 6P4-, and PSC-RANTES). We found that CCR5 signaled through both Gi/o and Gq/11 IP1 accumulation and Ca2+ flux arose from Gq/11 activation, rather than from Gβγ subunit release after Gi/o activation as had been previously proposed. The 6P4- and PSC-RANTES analogs were superagonists for Gq/11 activation, whereas the 5P12- and 5P14-RANTES analogs displayed a signaling bias for Gi/o These results demonstrate that RANTES analogs elicit G protein subtype-specific signaling bias and can cause CCR5 to couple preferentially to Gq/11 rather than to Gi/o signaling pathways. We propose that G protein subtype-specific signaling bias may be a general feature of GPCRs that can couple to more than one G protein family.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Calcium / metabolism
  • Chemokine CCL3 / pharmacology
  • Chemokine CCL5 / pharmacology
  • Chemokines / metabolism*
  • Cyclic AMP / metabolism
  • GTP-Binding Protein alpha Subunits, Gi-Go / metabolism
  • GTP-Binding Protein alpha Subunits, Gq-G11 / metabolism
  • HEK293 Cells
  • HIV-1 / metabolism
  • Humans
  • Inflammation
  • Inositol Phosphates / metabolism
  • Ligands
  • Peptides, Cyclic / pharmacology
  • Receptors, CCR5 / metabolism*
  • Signal Transduction*
  • Transfection

Substances

  • CCR5 protein, human
  • Chemokine CCL3
  • Chemokine CCL5
  • Chemokines
  • Inositol Phosphates
  • Ligands
  • Peptides, Cyclic
  • Receptors, CCR5
  • YM-254890
  • inositol 1-phosphate
  • Cyclic AMP
  • GTP-Binding Protein alpha Subunits, Gi-Go
  • GTP-Binding Protein alpha Subunits, Gq-G11
  • Calcium