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

During the process of aging, the fraction of CD4(+) T Cells with a naive phenotype, that is, Pgp-1(-) CD45RB(High)MEL-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 cell...

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Detalles Bibliográficos
Autores principales: Nagelkerken, Lex, Hertogh-Huijbregts, Anita
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 1992
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2275905/
https://www.ncbi.nlm.nih.gov/pubmed/1364177
http://dx.doi.org/10.1155/1992/31573
Descripción
Sumario:During the process of aging, the fraction of CD4(+) T Cells with a naive phenotype, that is, Pgp-1(-) CD45RB(High)MEL-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.