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Function of Heterogeneous Nuclear Ribonucleoprotein U and related MicroRNAs in Human Coronary Artery Endothelial Cells and Endothelial Microparticles

dc.contributor.advisorWerner, Nikos
dc.contributor.authorWang, Han
dc.date.accessioned2020-04-23T08:47:32Z
dc.date.available2020-04-23T08:47:32Z
dc.date.issued18.12.2017
dc.identifier.urihttps://hdl.handle.net/20.500.11811/6990
dc.description.abstractThe protein heterogeneous nuclear ribonucleoprotein U (hnRNP U) plays an essential role in the development and function of the heart. The hnRNP U protein in human coronary artery endothelial cells (HCAEC) mediates its function by binding microRNAs (miRNAs). Endothelial microparticles (EMP) derived from HCAEC regulate several processes in cardiovascular biology by transferring miRNAs to target cells. In this study, we aimed to explore the function of hnRNP U in HCAEC and EMP.
We found that the hnRNP U protein binds to microRNA-30c (miRNA-30c) and microRNA-24 (miRNA-24) in HCAEC in vitro. Furthermore, the downregulation of hnRNP U in HCAEC decreases the levels of both miRNA-30c and miRNA-24. Downregulation of hnRNP U did not affect the number of EMP released from HCAEC. The miRNA-30c and miRNA-24 expression levels were higher in both EMP and the supernatant when transfected with si-hnRNP U compared to transfection with the siRNA negative control. EMP derived from HCAEC transfected with si-hnRNP U inhibit HCAEC migration and promote proliferation. Furthermore, upregulated miRNA-30c and miRNA-24 expression both inhibit HCAEC motility and promote proliferation in vitro.
HnRNP U protein binds to miRNA-30c and miRNA-24 in vitro. EMP derived from HCAEC cells transfected with si-hnRNP U negatively regulate HCAEC motility and positively promote proliferation.
dc.language.isoeng
dc.rightsIn Copyright
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/
dc.subject.ddc610 Medizin, Gesundheit
dc.titleFunction of Heterogeneous Nuclear Ribonucleoprotein U and related MicroRNAs in Human Coronary Artery Endothelial Cells and Endothelial Microparticles
dc.typeDissertation oder Habilitation
dc.publisher.nameUniversitäts- und Landesbibliothek Bonn
dc.publisher.locationBonn
dc.rights.accessRightsopenAccess
dc.identifier.urnhttps://nbn-resolving.org/urn:nbn:de:hbz:5n-48535
ulbbn.pubtypeErstveröffentlichung
ulbbnediss.affiliation.nameRheinische Friedrich-Wilhelms-Universität Bonn
ulbbnediss.affiliation.locationBonn
ulbbnediss.thesis.levelDissertation
ulbbnediss.dissID4853
ulbbnediss.date.accepted29.08.2017
ulbbnediss.instituteMedizinische Fakultät / Kliniken : Medizinische Klinik und Poliklinik II - Kardiologie, Angiologie, Pneumologie und Internistische Intensivmedizin
ulbbnediss.fakultaetMedizinische Fakultät
dc.contributor.coRefereeMüller, Stefan C.


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