Clinical and Surgical Pathology, Department of Specialty, Diagnostic and Experimental Medicine, S.Orsola-Malpighi Hospital, University of Bologna, via Massarenti 9, 40138, Bologna, Italy.
Vascular Surgery, Department of Specialty, Diagnostic and Experimental Medicine, S.Orsola-Malpighi Hospital, University of Bologna, via Massarenti 9, Bologna, 40138, Italy.
Virchows Arch. 2020 Feb;476(2):307-316. doi: 10.1007/s00428-019-02659-w. Epub 2019 Sep 10.
Arterial calcification is an actively regulated process, with different morphological manifestations. Micro-RNAs emerged as potential regulators of vascular calcification; they may become novel diagnostic tools and be used for a finest staging of the carotid plaque progression. The present study aimed at characterizing the different miRNA-mRNA axes in carotid plaques according to their histological patterns of calcification. Histopathological analysis was performed on 124 retrospective carotid plaques, with clinical data and preoperatory angio-CT. miRNA analysis was carried out with microfluidic cards. Real-time PCR was performed for selected miRNAs validation and for RUNX-2 and SOX-9 mRNA levels. CD31, CD68, SMA, and SOX-9 were analyzed by immunohistochemistry. miRNA levels on HUVEC cells were analyzed for confirming results under in vitro osteogenic conditions. Histopathological analysis revealed two main calcification subtypes of plaques: calcific cores (CC) and protruding nodules (PN). miRNA array and PCR validation of miR-1275, miR-30a-5p, and miR-30d indicated a significant upregulation of miR-30a-5p and miR-30d in the PN plaques. Likewise, the miRNA targets RUNX-2 and SOX-9 resulted poorly expressed in PN plaques. The inverse correlation between miRNA and RUNX-2 levels was confirmed on osteogenic-differentiated HUVEC. miR-30a-5p and miR-30d directly correlated with calcification extension and thickness at angio-CT imaging. Our study demonstrated the presence of two distinct morphological subtypes of calcification in carotid atheromatous plaques, supported by different miRNA signatures, and by different angio-CT features. These results shed the light on the use of miRNA as novel diagnostic markers, suggestive of plaque evolution.
动脉钙化是一个受调控的过程,具有不同的形态表现。microRNAs 作为血管钙化的潜在调节因子而出现;它们可能成为新的诊断工具,并用于对颈动脉斑块进展进行最精细的分期。本研究旨在根据颈动脉斑块的组织学钙化模式来描述不同的 miRNA-mRNA 轴。对 124 例回顾性颈动脉斑块进行了组织病理学分析,同时进行了临床数据和术前血管 CT 检查。采用微流控卡进行 miRNA 分析。对选定的 miRNA 进行实时 PCR 验证,并对 RUNX-2 和 SOX-9 mRNA 水平进行检测。通过免疫组织化学分析 CD31、CD68、SMA 和 SOX-9。在体外成骨条件下对 HUVEC 细胞中的 miRNA 水平进行分析,以验证结果。组织病理学分析显示斑块有两种主要的钙化亚型:钙化核心(CC)和突出结节(PN)。miRNA 阵列和 miR-1275、miR-30a-5p 和 miR-30d 的 PCR 验证表明,PN 斑块中 miR-30a-5p 和 miR-30d 的表达显著上调。同样,PN 斑块中 miRNA 靶标 RUNX-2 和 SOX-9 的表达水平也较低。在成骨分化的 HUVEC 中证实了 miRNA 与 RUNX-2 水平之间的负相关。miR-30a-5p 和 miR-30d 与血管 CT 成像中的钙化扩展和厚度直接相关。我们的研究表明,在颈动脉粥样硬化斑块中存在两种不同的形态钙化亚型,这两种亚型由不同的 miRNA 特征和不同的血管 CT 特征支持。这些结果为 miRNA 作为新的诊断标志物的应用提供了依据,提示了斑块的演变。