The Acquisition of a Memory Phenotype by Murine CD4+T Cells Is Accompanied by a Loss in Their Capacity to Increase Intracellular Calcium

Author:

Nagelkerken Lex1,Hertogh-Huijbregts Anita1

Affiliation:

1. Section of Immunology, TNO Institute of Aging and Vascular Research TNO, P.O. Box 430, Leiden 2300 AK, The Netherlands

Abstract

During the process of aging, the fraction of CD4+T Cells with a naive phenotype, that is, Pgp-1-CD45RBHighMEL-14+, decreases in favor of CD4+T memory cells. Total CD4+T cells from aged mice displayed a diminished calcium response to anti-CD3 and even ionomycin as compared to the cells from young mice, and this was related to the changed composition of the CD4+T-cell population. Regardless the age of the donor mice, naive CD4+T cells effectively increased intracellular calcium, whereas memory CD4+T cells were impaired in this regard. In addition, a heterogeneity in the differentiation stage of the naive CD4+T cells was shown by the observation that calcium mobilization in naive CD4+T cells from young mice was more profound than that in their aged counterparts. These data thus indicate that during the acquisition of a memory phenotype, murine CD4+T cells lose the capacity to increase intracellular calcium, which in turn may be responsible for the decreased level of IL-2 production by these cells.

Publisher

Hindawi Limited

Subject

Developmental Biology,Immunology

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