Publication:
Implementation of the EGFP-K562 flow cytometric NK test: Determination of NK cytotoxic activity in healthy elderly volunteers before and after feeding

dc.contributor.authorSéverine Allegraen_US
dc.contributor.authorCécile Deleineen_US
dc.contributor.authorRime Michael-Jubelyen_US
dc.contributor.authorCéline Grysonen_US
dc.contributor.authorYves Boirieen_US
dc.contributor.authorWannee Kantakamalakulen_US
dc.contributor.authorMarie Paule Vassonen_US
dc.contributor.otherUniversite d'Auvergne, Faculte de Medecine Clermont-Ferranden_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherCentre Jean Perrinen_US
dc.date.accessioned2018-08-20T06:50:10Z
dc.date.available2018-08-20T06:50:10Z
dc.date.issued2006-09-01en_US
dc.description.abstractBackground: Natural Killer (NK) cells are key actors of innate immunity that supervise the organism's cells, and fight against viral infections and cancer development through their cytotoxic activity. This cytotoxic activity is modulated by cytokines and hormones and could be influenced by physiological or pathological conditions. New techniques for measuring NK cytotoxic activity by flow-cytometry have recently been developed, and they correlated strongly with the standard chromium ( 51Cr) release assay. Our aim was to implement a previously published enhanced green fluorescent protein (EGFP)-K562 flow cytometric method and use it to evaluate NK cytotoxic activity under different nutritional conditions. Methods: NK effector cells were isolated from peripheral blood mononuclear cells, and a K562 cell line stably transfected by EGFP was used as target cells. Different analytical parameters, including cell ratios and incubation times, were studied to improve the EGFP-K562 flow cytometric NK test conditions. Results: The optimized test was then used to determine the effect of fasting and refeeding on NK cell numbers and activity in a physiological situation. NK cytotoxic activity in fasted conditions (30.4 ± 4.4%) increased by a factor 1.7 ± 0.2 (P = 0.0025) in nourished conditions (45.0 ± 4.6%) in healthy elderly people. Conclusion: Therefore, this method provides a reliable, reproducible and rapid test for analyzing NK cytotoxicity under various conditions. © 2006 International Society for Analytical Cytology.en_US
dc.identifier.citationCytometry Part A. Vol.69, No.9 (2006), 992-998en_US
dc.identifier.doi10.1002/cyto.a.20301en_US
dc.identifier.issn15524930en_US
dc.identifier.issn15524922en_US
dc.identifier.other2-s2.0-33749470542en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/22989
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33749470542&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleImplementation of the EGFP-K562 flow cytometric NK test: Determination of NK cytotoxic activity in healthy elderly volunteers before and after feedingen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33749470542&origin=inwarden_US

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