کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2088314 | 1545711 | 2013 | 6 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Analysis of cytokines and chemokines produced by whole blood, peripheral mononuclear and polymorphonuclear cells Analysis of cytokines and chemokines produced by whole blood, peripheral mononuclear and polymorphonuclear cells](/preview/png/2088314.png)
• Cytokine expression profiles of whole blood, PBMCs and PMNs after LPS stimulation.
• CCL11 and IL-23 were only expressed in whole blood.
• IL-20, VEGF and GM-CSF were only expressed by PBMC.
• Different experimental settings lead to different results, investigate before performing your experiment.
Cytokines are immunomodulating proteins involved in cellular communication. The levels of different cytokines reflect the immune capabilities of a person. In literature both whole blood and peripheral blood mononuclear cells (PBMCs) are used, which might lead to different results. The choice between these different sources is not always explained. The goal of our experiments is to determine the cytokine response of whole blood, PBMCs and polymorphonuclear cells (PMNs) after stimulation with lipopolysaccharide (LPS). We used a multiplex analysis to determine a difference in cytokine secretion patterns. In general, PBMCs demonstrated the highest cytokine production and PMNs have an overall low cytokine production. CCL11 and interleukin-23 (IL-23) (and IL-12p40) were exclusively expressed in whole blood. IL-20, VEGF and GM-CSF were expressed only by PBMCs. This difference in expression could be explained by the bioactive components in serum, presence and interaction with granulocytes or platelets in whole blood, the anticoagulant heparin in whole blood and others. The expression of cytokines by cells is dependent on the microenvironment. Different conditions lead to different results. We recommend a thorough examination of the conditions before performing experiments.
Journal: Journal of Immunological Methods - Volume 396, Issues 1–2, 31 October 2013, Pages 128–133