The G protein beta 3 subunit splice variant G beta 3-s causes enhanced chemotaxis of human neutrophils in response to interleukin-8

A C825T polymorphism was recently described in GNB3, the gene encoding the G beta 3 subunit of heterotrimeric G proteins. The 825T allele is associate d with the expression of a shorter splice variant (G beta 3-s) and enhanced signal transduction via pertussis toxin (PTX)sensitive G proteins. Given t he pivotal role of G protein py dimers in chemotaxis, we related the genoty pe at the GNB3 locus as a marker for G beta 3-s expression to chemotaxis of human neutrophils in response to stimulation with interleukin-8 (IL-8). IL -8, which activates a CXC receptor coupled to PTX-sensitive G proteins, ind uced at 10 nM an enhanced maximum chemotaxis of neutrophils from individual s with TC/TT genotype compared to CC genotype. Furthermore, migration of ne utrophils from 825T allele carriers was 2.5-fold higher at 0.1 nM and 1 nM IL-8. At these concentrations of IL-8, no significant chemotaxis was observ ed in neutrophils from homozygous C825 allele carriers, indicating a genoty pe-dependent, different potency of IL-8 to chemoattract neutrophils. In con trast, IL-X-induced Ca2+ signals and O2- generation were independent of gen otype. The role of G beta 3-s in enhanced chemotaxis could be confirmed by determination of chemotaxis of COS-7 cells following transfection with eith er G beta 3-s or "wild-type" G beta 3. Upon stimulation of the transfected cells with the chemoattractant lysophosphatidic acid (LPA), we observed an enhanced chemotactic response of G beta 3-s-transfected compared to G beta 3-transfected COS-7 cells, confirming that G beta 3-s actually causes enhan ced chemotaxis.