Regulation of thymus-dependent and thymus-independent production of immunoglobulin G subclasses by Galpha12 and Galpha13

Background: A previous study from this laboratory showed that Gα₁₂ members participate in the production of inflammatory cytokines. In spite of the identification of B cell homeostasis responses regulated by Gα₁₃, the functional roles of Gα₁₂ members in the production of immunoglobulin (Ig) isotypes remained unknown. This study investigated whether Gα₁₂ members are involved in the Ig isotype antibody production with the purpose of establishing their functions in thymus-dependent and thymus-independent humoral responses.

Results: Mice lacking Gα₁₂ and/or Gα₁₃ showed an impaired antigen-specific antibody production promoted by challenge(s) of ovalbumin or trinitrophenyl-lipopolysaccharide (TNP-LPS), used for thymus-dependent and thymus-independent stimuli, respectively. Homozygous knockout (KO) of Gα₁₂ or double heterozygous KO of Gα₁₂/Gα₁₃ significantly reduced the antigen-specific total IgG level after multiple ovalbumin immunizations with decreases in the production of IgG1, IgG2a and IgG2b subclasses, as compared to wild type control. In contrast, IgM production was not decreased. Moreover, mice deficient in Gα₁₂ or partially deficient in Gα₁₃ or Gα₁₂/Gα₁₃ showed significantly low production of IgG2b in response to TNP-LPS. In TNP-LPS-injected mice, IgG1 and IgG2a productions were unaffected by the G protein KOs.

Conclusion: Our results demonstrate that both Gα₁₂ and Gα₁₃ are essentially involved in thymusdependent and independent production of IgG subclasses, implying that the G-proteins contribute to the process of antigen-specific IgG antibody production.