Regulators of G protein signaling exhibit distinct patterns of gene expression and target G protein specificity in human lymphocytes.
The newly recognized regulators of G protein signaling (RGS) attenuate heterotrimeric G protein signaling pathways. We have cloned an IL-2-induced gene from human T cells, cytokine-responsive gene 1, which encodes a member of the RGS family, RGS16. The RGS16 protein binds Gialpha and Gqalpha proteins present in T cells, and ... inhibits Gi- and Gq-mediated signaling pathways. By comparison, the mitogen-induced RGS2 inhibits Gq but not Gi signaling. Moreover, the two RGS genes exhibit marked differences in expression patterns. The IL-2-induced expression of the RGS16 gene in T cells is suppressed by elevated cAMP, whereas the RGS2 gene shows a reciprocal pattern of regulation by these stimuli. Because the mitogen and cytokine receptors that trigger expression of RGS2 and RGS16 in T cells do not activate heterotrimeric G proteins, these RGS proteins and the G proteins that they regulate may play a heretofore unrecognized role in T cell functional responses to Ag and cytokine activation.
Mesh Terms:
Cells, Cultured, Cyclic AMP, GTP-Binding Proteins, Humans, Lymphocytes, Proteins, RGS Proteins, Receptors, Interleukin-2
Cells, Cultured, Cyclic AMP, GTP-Binding Proteins, Humans, Lymphocytes, Proteins, RGS Proteins, Receptors, Interleukin-2
J. Immunol.
Date: Mar. 01, 1999
PubMed ID: 10072511
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