Quantitative and integrated proteome and microRNA analysis of endothelial replicative senescence

•Proteome and miRNAome profiles are altered during the progression of endothelial replicative senescence.•Integrated data analysis shows interaction between miRNA and protein expression.•Senescence-related changes in the endothelial proteome are regulated by alteration in miRNA levels.•Affected pathways include changes in the metabolism, cell cycle and structural organization.•These pathways may contribute to increased risk of age-related cardiovascular disease.

Age-related changes in vascular functioning are a harbinger of cardiovascular disease but the biological mechanisms during the progression of endothelial senescence have not been studied. We investigated alterations in the proteome and miRNA profiles in the course of replicative senescence using primary human umbilical vein endothelial cells as an in vitro vascular model. Quantitative proteomic profiling from early growth stage to senescence was performed by isotope-coded protein label coupled to LC-ESI-MS/MS analysis. Some proteins consistently changed their expression during the senescence whereas others appeared as deregulated only during the late senescence. The latter was accompanied by alterations in morphology of senescent endothelial cells. MicroRNA expression profiling revealed transient changes in the level of miR-16-5p, miR-28-3p and miR-886-5p in the early senescence, decrease in the level of miR-106b-3p at the late stage, and continuous changes in the expression of miR-181a-5p and miR-376a-3p during the whole senescence process. Integrating data on proteomic and microRNA changes indicated potential crosstalk between specific proteins and non-coding RNAs in the regulation of metabolism, cell cycle progression and cytoskeletal organization in the endothelial senescence. The knowledge of molecular targets that change during the senescence can ultimately contribute to a better understanding and prevention of age-related vascular diseases.

Graphical abstractFigure optionsDownload full-size imageDownload high-quality image (175 K)Download as PowerPoint slide