Sarad Katarzyna, Jankowska Urszula, Skupien-Rabian Bozena, Babler Anne, Kramann Rafael, Dulak Józef, Jaźwa-Kusior Agnieszka
Department of Medical Biotechnology, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Gronostajowa Str. 7, 30-387, Krakow, Poland.
Doctoral School of Exact and Natural Sciences, Jagiellonian University, Kraków, Poland.
Mol Cell Biochem. 2025 Feb;480(2):1027-1043. doi: 10.1007/s11010-024-05028-7. Epub 2024 May 14.
Aging is the most important risk factor for the development of cardiovascular diseases. Senescent cells release plethora of factors commonly known as the senescence-associated secretory phenotype, which can modulate the normal function of the vascular wall. It is currently not well understood if and how endothelial cell senescence can affect adventitial niche. The aim of this study was to characterize oxidative stress-induced endothelial cells senescence and identify their paracrine effects on the primary cell type of the adventitia, the fibroblasts. Human aortic endothelial cells (HAEC) were treated with hydrogen peroxide to induce premature senescence. Mass spectrometry analysis identified several proteomic changes in senescent HAEC with top upregulated secretory protein growth differentiation factor 15 (GDF-15). Treatment of the human adventitial fibroblast cell line (hAdv cells) with conditioned medium (CM) from senescent HAEC resulted in alterations in the proteome of hAdv cells identified in mass spectrometry analysis. Majority of differentially expressed proteins in hAdv cells treated with CM from senescent HAEC were involved in the uptake and metabolism of lipoproteins, mitophagy and ferroptosis. We next analyzed if some of these changes and pathways might be regulated by GDF-15. We found that recombinant GDF-15 affected some ferroptosis-related factors (e.g. ferritin) and decreased oxidative stress in the analyzed adventitial fibroblast cell line, but it had no effect on erastin-induced cell death. Contrary, silencing of GDF-15 in hAdv cells was protective against this ferroptotic stimuli. Our findings can be of importance for potential therapeutic strategies targeting cell senescence or ferroptosis to alleviate vascular diseases.
衰老是心血管疾病发生发展的最重要风险因素。衰老细胞会释放大量通常被称为衰老相关分泌表型的因子,这些因子可调节血管壁的正常功能。目前对于内皮细胞衰老是否以及如何影响外膜微环境尚不清楚。本研究的目的是表征氧化应激诱导的内皮细胞衰老,并确定其对外膜主要细胞类型成纤维细胞的旁分泌作用。用人主动脉内皮细胞(HAEC)用过氧化氢处理以诱导过早衰老。质谱分析确定了衰老的HAEC中几种蛋白质组学变化,其中分泌蛋白生长分化因子15(GDF-15)上调最为明显。用衰老HAEC的条件培养基(CM)处理人外膜成纤维细胞系(hAdv细胞),导致质谱分析中鉴定出hAdv细胞蛋白质组发生改变。用衰老HAEC的CM处理的hAdv细胞中,大多数差异表达蛋白参与脂蛋白的摄取和代谢、线粒体自噬和铁死亡。接下来,我们分析了其中一些变化和途径是否可能受GDF-15调节。我们发现重组GDF-15影响了一些与铁死亡相关的因子(如铁蛋白),并降低了所分析的外膜成纤维细胞系中的氧化应激,但对埃拉斯汀诱导的细胞死亡没有影响。相反,在hAdv细胞中沉默GDF-15可保护细胞免受这种铁死亡刺激。我们的发现对于针对细胞衰老或铁死亡的潜在治疗策略以缓解血管疾病可能具有重要意义。