Microarray analysis of senescent vascular smooth muscle cells: A link to atherosclerosis and vascular calcification

作者：Burton Dominick G A; Giles Peter J; Sheerin Angela N P; Smith S Kaye; Lawton Jessica J; Ostler Elizabeth L; Rhys Williams William; Kipling David; Faragher Richard G A^*

来源：Experimental Gerontology, 2009, 44(10): 659-665.

DOI：10.1016/j.exger.2009.07.004

• Vascular calcification
• Atherosclerosis
• Cellular senescence
• Ageing
• Cardiovascular disease
• Vascular smooth muscle

Little is known about the senescent phenotype of human vascular smooth muscle cells (VSMCs) and the potential involvement of senescent VSMCs in age-related vascular disease, such as atherosclerosis. As such, VSMCs were grown and characterised in vitro to generate senescent VSMCs needed for microarray analysis (Affymetrix). Comparative analysis of the transcriptome profiles of early (14 CPD) and late (39-42 CPD) passage VSMCs found a total of 327 probesets called as differentially expressed: 149 are up-regulated in senescence and 178 repressed (p-value < 0.5%, minimum effect size of at least 2-fold differential regulation, explore data at http://www.madras.cf.ac.uk/vsmc). Data mining shows a differential regulation of genes at senescence associated with the development of atherosclerosis and vascular calcification. These included genes with roles in inflammation (IL1 beta, IL8, ICAM1, TNFAP3, ESM1 and CCL2), tissue remodelling (VEGF, VEGF beta, ADM and MMP14) and vascular calcification (MGP, BMP2, SPP1, OPG and DCN). The microarray data for IL1 beta, IL8 and MGP were validated by either, ELISA, Western blot analysis or RT-PCR. These data thus provide the first evidence for a role of VSMC senescence in the development of vascular calcification and provides further support for the involvement of senescent VSMCs in the progression of atherosclerosis.

• 出版日期2009-10