Egyszerű nézet

dc.contributor.author Kollár, Szonja
dc.contributor.author Berta L
dc.contributor.author Vasarhelyi ZE
dc.contributor.author Balog, Attila
dc.contributor.author Vásárhelyi, Barna
dc.contributor.author Rigó, János Jr
dc.contributor.author Toldi, Gergely
dc.date.accessioned 2016-06-27T11:32:19Z
dc.date.available 2016-06-27T11:32:19Z
dc.date.issued 2015
dc.identifier 84931069681
dc.identifier.citation pagination=13750-13756; journalVolume=6; journalIssueNumber=15; journalTitle=ONCOTARGET;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/2147
dc.description.abstract Adaptive immunity and T cell function are affected by aging. Calcium influx patterns, regulated by Kv1.3 and IKCa1 potassium channels, influence T cell activation. We aimed to compare calcium influx kinetics in CD8, Th1 and Th2 cells in human peripheral blood samples obtained from five different age groups (cord blood, 10-15 ys, 25-40 ys, 45-55 ys, 60-75 ys).We measured calcium influx using flow cytometry in samples treated with or without specific inhibitors of Kv1.3 and IKCa1 channels (MGTX and TRAM, respectively).Calcium influx was higher in Th1 cells of adults, however, its extent decreased again with aging. Importantly, these changes were not detected in Th2 cells, where the pattern of calcium influx kinetics is similar throughout all investigated age groups. MGTX had a more pronounced inhibitory effect on calcium influx in Th2 cells, while in Th1 cells the same was true for TRAM in the 25-40 ys and 45-55 ys groups. Calcium influx of CD8 cells were inhibited to a similar extent by both applied inhibitors in these groups, and had no effect in the elderly.Altered lymphocyte potassium channel inhibitory patterns, regulators of calcium influx kinetics, might contribute to the development of age-related changes of T cell function.
dc.relation.ispartof urn:issn:1949-2553
dc.title Impact of aging on calcium influx and potassium channel characteristics of T lymphocytes.
dc.type Journal Article
dc.date.updated 2015-08-31T09:34:24Z
dc.language.rfc3066 en
dc.identifier.mtmt 2891853
dc.identifier.pubmed 25948778
dc.contributor.department SE/AOK/K/II. Sz. Szülészeti és Nőgyógyászati Klinika
dc.contributor.department SE/AOK/K/I. Sz. Szülészeti és Nőgyógyászati Klinika
dc.contributor.department SE/AOK/I/Laboratóriumi Medicina Intézet
dc.contributor.department SE/AOK/K/I. Sz. Gyermekgyógyászati Klinika
dc.contributor.department SE/AOK/K/ISZGYK/MTA-SE Gyermekgyógyászati és Nephrológiai Kutatócsoport
dc.contributor.institution Semmelweis Egyetem


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