| Literature DB >> 26874686 |
Eva C Schwarz1, Christina Backes2, Arne Knörck1, Nicole Ludwig3, Petra Leidinger3, Cora Hoxha1, Gertrud Schwär1, Thomas Grossmann4, Sabine C Müller4, Martin Hart3, Jan Haas5,6,7, Valentina Galata4, Isabelle Müller8, Tobias Fehlmann4, Hermann Eichler8, Andre Franke9, Benjamin Meder5,6,7, Eckart Meese3, Markus Hoth1, Andreas Keller4.
Abstract
A systematic understanding of different factors influencing cell type specific microRNA profiles is essential for state-of-the art biomarker research. We carried out a comprehensive analysis of the biological variability and changes in cell type pattern over time for different cell types and different isolation approaches in technical replicates. All combinations of the parameters mentioned above have been measured, resulting in 108 miRNA profiles that were evaluated by next-generation-sequencing. The largest miRNA variability was due to inter-individual differences (34 %), followed by the cell types (23.4 %) and the isolation technique (17.2 %). The change over time in cell miRNA composition was moderate (<3 %) being close to the technical variations (<1 %). Largest variability (including technical and biological variance) was observed for CD8 cells while CD3 and CD4 cells showed significantly lower variations. ANOVA highlighted that 51.5 % of all miRNAs were significantly influenced by the purification technique. While CD4 cells were least affected, especially miRNA profiles of CD8 cells were fluctuating depending on the cell purification approach. To provide researchers access to the profiles and to allow further analyses of the tested conditions we implemented a dynamic web resource.Entities:
Keywords: Blood cells; FACS; Next-generation sequencing; microRNA
Mesh:
Substances:
Year: 2016 PMID: 26874686 DOI: 10.1007/s00018-016-2154-9
Source DB: PubMed Journal: Cell Mol Life Sci ISSN: 1420-682X Impact factor: 9.261