International Immunology Advance Access published online on July 6, 2005
International Immunology, doi:10.1093/intimm/dxh279
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1 Department of Biological Chemistry, University of Michigan Medical School, Ann Arbor, MI, USA; Present address: 5410 CCGCB, 1500 East Medical Center Drive, Ann Arbor, MI 48109-0940, USA
* To whom correspondence should be addressed. Many of the downstream signaling defects observed in aged T cells are believed to be the result of very early events involving the initial interaction between T cells and antigen-presenting cells. Recent findings suggest that this interaction is hindered by glycosylated surface macromolecules, including CD43, on the T cell surface. Treatment of CD4+ T cells by O-sialoglycoprotein endopeptidase (OSGE), which cleaves glycosylated forms of CD43, restores the ability of cells from aged mice to form immunological synapses and to express early activation markers. Here we show that OSGE enhances Ca2+ influx in T cells from CB6F1 mice, and enhances their ability to produce IL-2, IL-4, IL-5, IL-6, IL-10, IL-13 and IFN
Received September 22, 2004
Accepted May 10, 2005
Article
A glycoprotein endopeptidase enhances calcium influx and cytokine production by CD4+ T cells of old and young mice
2 Department of Pathology, University of Michigan Medical School, Ann Arbor, MI, USA
3 Department of Pathology, University of Michigan Medical School, Ann Arbor, MI, USA; Geriatrics Center, University of Michigan, Ann Arbor, MI, USA; Ann Arbor DVA Medical Center, Ann Arbor, MI 48109-0940, USA
Scott B. Berger, E-mail: bergers{at}umich.edu
Abstract 
at the mRNA level, and IL-2 and IFN at the protein level, in the first 6 h after activation. Although OSGE has little effect on synapse formation in CD4+ T cells from young mice, our new data show that OSGE increases the production of most cytokines by young as well as old T cells. Secretion of the Th2 cytokine, IL-4, was altered only slightly by OSGE treatment, suggesting that the removal of OSGE-sensitive surface molecules may have differential effects on Th1 and Th2 cytokines. These data support a model in which O-glycosylated surface proteins inhibit CD4+ lymphocyte activation in both young and old mice, and in which such glycoproteins contribute to the age-related decline in cytokine production.
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