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Regulation of T Cell Activation, Anxiety, and Male Aggression by RGS2

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Specialty Science
Date 2000 Oct 12
PMID 11027316
Citations 97
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Abstract

Regulators of G protein signaling (RGS) proteins accelerate the GTPase activity of Galpha protein subunits in vitro, negatively regulating G protein-coupled receptor signaling. The physiological role of mammalian RGS proteins is largely unknown. The RGS family member rgs2 was cloned as an immediate early response gene up-regulated in T lymphocytes after activation. To investigate the role of RGS2 in vivo, we generated rgs2-deficient mice. We show that targeted mutation of rgs2 in mice leads to reduced T cell proliferation and IL-2 production, which translates in an impaired antiviral immunity in vivo. Interestingly, rgs2(-/-) mice also display increased anxiety responses and decreased male aggression in the absence of cognitive or motor deficits. RGS2 also controls synaptic development and basal electrical activity in hippocampal CA1 neurons. Thus, RGS2 plays an important role in T cell activation, synapse development in the hippocampus, and emotive behaviors.

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References
1.
Chen C, Burns M, He W, Wensel T, Baylor D, Simon M . Slowed recovery of rod photoresponse in mice lacking the GTPase accelerating protein RGS9-1. Nature. 2000; 403(6769):557-60. DOI: 10.1038/35000601. View

2.
Siderovski D, Strockbine B, Behe C . Whither goest the RGS proteins?. Crit Rev Biochem Mol Biol. 1999; 34(4):215-51. DOI: 10.1080/10409239991209273. View

3.
GILMAN A . G proteins: transducers of receptor-generated signals. Annu Rev Biochem. 1987; 56:615-49. DOI: 10.1146/annurev.bi.56.070187.003151. View

4.
White N, McDonald R . Acquisition of a spatial conditioned place preference is impaired by amygdala lesions and improved by fornix lesions. Behav Brain Res. 1993; 55(2):269-81. DOI: 10.1016/0166-4328(93)90122-7. View

5.
Siderovski D, Heximer S, Forsdyke D . A human gene encoding a putative basic helix-loop-helix phosphoprotein whose mRNA increases rapidly in cycloheximide-treated blood mononuclear cells. DNA Cell Biol. 1994; 13(2):125-47. DOI: 10.1089/dna.1994.13.125. View