<?xml version="1.0" encoding="ASCII"?>
<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="species">human</item><item key="factors"><item><item key="GSM813068"><item key="GENDER">female</item><item key="AGE">28</item></item></item><item><item key="GSM813069"><item key="GENDER">female</item><item key="AGE">80</item></item></item><item><item key="GSM813070"><item key="GENDER">male</item><item key="AGE">79</item></item></item><item><item key="GSM81307"><item key="GENDER">female</item><item key="AGE">46</item></item></item></item><item key="id">4255</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">4</item><item key="summary_wrapped">Recently, the bone marrow (BM) has been shown to play a key role in regulating the survival and function of memory T cells. However, the...</item><item key="geo_gse_id">E-GEOD-32725</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">2</item><item key="sample_count">4</item><item key="tags"><item>bone</item><item>bone marrow</item><item>cell</item><item>line</item><item>peripheral</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">the-impact-of-aging-on-memory-t-cell-phenotype-and</item><item key="geo_id_plat">E-GEOD-32725_A-AFFY-44</item><item key="name">The impact of aging on memory T cell phenotype and function in the human bone marrow</item><item key="created">Sep.16, 2014</item><item key="summary">Recently, the bone marrow (BM) has been shown to play a key role in regulating the survival and function of memory T cells. However, the impact of aging on these processes has not yet been studied. We demonstrate that the number of CD4+ and CD8+ T cells in the BM is maintained during aging. However, the composition of the T cell pool in the aged BM is altered with a decline of na&#239;ve and an increase in effector-memory T cells. In contrast to the peripheral blood (PB), a highly activated CD8+CD28&#8211; T cell population, which lacks the late differentiation marker CD57, accumulates in the BM of elderly persons. IL-6 and IL-15, which are both increased in the aged BM, efficiently induce the activation, proliferation and differentiation of CD8+ T cell in vitro, highlighting a role of these cytokines in the age-dependent accumulation of highly activated CD8+CD28&#8211; T cells in the BM. Yet, these age-related changes do not impair the maintenance of a high number of polyfunctional memory CD4+ and CD8+ T cells in the BM of elderly persons. In summary, aging leads to the accumulation of a highly activated CD8+CD28&#8211; T cell population in the BM, which is driven by the age-related increase of IL-6 and IL-15. Despite these changes, the aged BM is a rich source of polyfunctional memory T cells and may thus represent an important line of defense to fight recurrent infections in old age. A total of 4 samples (bone marrow mononuclear cells) were analyzed (2 young and 2 elderly persons)</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-32725</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-32725/samples/</item></data></biogps>
