From the Department of Molecular Medicine and Surgery (L.P., E.H., A.R., M.L., C.O., U.H.), and Department of Medicine (G.P.-B., J.O.), Karolinska Institute, Stockholm, Sweden; Department of Molecular Genetics, Novo Nordisk, Copenhagen, Denmark (L.F.); Department of Surgery, Södersjukhuset, Stockholm, Sweden (P.G.); Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden (F.P.); and Department of Proteomics, Royal Institute of Technology, Stockholm, Sweden (J.O.).
Arterioscler Thromb Vasc Biol. 2013 Oct;33(10):2432-43. doi: 10.1161/ATVBAHA.113.301743. Epub 2013 Aug 1.
Carotid plaque instability is a major cause of ischemic stroke, but detailed knowledge about underlying molecular pathways is still lacking. Here, we evaluated large-scale transcriptomic and protein expression profiling in a biobank of carotid endarterectomies followed by characterization of identified candidates, as a platform for discovery of novel proteins differentially regulated in unstable carotid lesions.
Genes highly upregulated in symptomatic versus asymptomatic plaques were selected from Affymetrix microarray analyses (n=127 plaques), and tissue microarrays constructed from 34 lesions were assayed for 21 corresponding proteins by immunohistochemistry. Quantification of stainings demonstrated differential expression of CD36, CD137, and DOCK7 (P<0.05) in unstable versus stable lesions and the most significant upregulation of a proprotein convertase, PCSK6 (P<0.0001). Increased expression of PCSK6 in symptomatic lesions was verified by quantitative real-time polymerase chain reaction (n=233), and the protein was localized to smooth muscle α-actin positive cells and extracellular matrix of the fibrous cap by immunohistochemistry. PCSK6 expression positively correlated to genes associated with inflammation, matrix degradation, and mitogens in microarrays. Stimulation of human carotid smooth muscle cells in vitro with cytokines caused rapid induction of PCSK6 mRNA.
Using a combination of transcriptomic and tissue microarray profiling, we demonstrate a novel approach to identify proteins differentially expressed in unstable carotid atherosclerosis. The proprotein convertase PCSK6 was detected at increased levels in the fibrous cap of symptomatic carotid plaques, possibly associated with key processes in plaque rupture such as inflammation and extracellular matrix remodeling. Further studies are needed to clarify the role of PCSK6 in atherosclerosis.
颈动脉斑块不稳定是缺血性卒中的主要原因,但对潜在的分子途径仍知之甚少。在此,我们通过对颈动脉内膜切除术的生物样本库进行大规模转录组和蛋白质表达谱分析,并对鉴定出的候选物进行特征分析,以此作为发现不稳定颈动脉病变中差异调节的新型蛋白质的平台。
从 Affymetrix 微阵列分析中选择在有症状斑块与无症状斑块中高表达的基因(n=127 个斑块),并通过免疫组织化学法对 34 个病变构建的组织微阵列检测 21 个相应蛋白质。染色的定量分析显示,不稳定病变中 CD36、CD137 和 DOCK7 的表达有差异(P<0.05),而前蛋白转化酶 PCSK6 的表达上调最为显著(P<0.0001)。通过定量实时聚合酶链反应(n=233)验证了 PCSK6 在有症状病变中的表达增加,并通过免疫组织化学法将其定位到平滑肌α-肌动蛋白阳性细胞和纤维帽的细胞外基质中。PCSK6 的表达与微阵列中与炎症、基质降解和有丝分裂原相关的基因呈正相关。体外用细胞因子刺激人颈动脉平滑肌细胞可迅速诱导 PCSK6 mRNA 的表达。
我们使用转录组和组织微阵列分析相结合的方法,提出了一种鉴定不稳定颈动脉粥样硬化中差异表达蛋白的新方法。在有症状颈动脉斑块的纤维帽中检测到前蛋白转化酶 PCSK6 水平升高,可能与斑块破裂的关键过程有关,如炎症和细胞外基质重塑。需要进一步研究来阐明 PCSK6 在动脉粥样硬化中的作用。