晚期颈动脉粥样硬化内膜上调 Natriuretic Peptide Receptor-C

Journal of medical & surgical pathology Pub Date : 2016-07-01 Epub Date: 2016-07-05 DOI:10.4172/2472-4971.1000131
Mohamed A Zayed, Scott D Harring, Dana R Abendschein, Chandu Vemuri, Dongsi Lu, Lisa Detering, Yongjian Liu, Pamela K Woodard
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摘要

目的:钠尿肽受体-C(NPR-C/NPR-3)是一种参与血管重塑的细胞表面蛋白,在动脉粥样硬化中被上调。在人类颈动脉闭塞病变中,NPR-C 的表达尚未得到很好的描述。我们假设 NPR-C 的表达与易损动脉粥样硬化颈动脉斑块的内膜特征相关:为了验证这一假设,我们通过免疫组化(IHC)评估了从 18 名患者分离的颈动脉内膜切除术(CEA)标本中 NPR-C 的表达。我们使用两种组织分析技术对 CEA 标本中 NPR-C 的等级、位置和共定位进行了评估:结果:相对于轻度病变的CEA标本,我们在重度病变的CEA标本内膜中观察到了大量的NPR-C组织染色(65%;P=0.06)。具体来说,病变最严重的 CEA 标本在浅层内膜(61%,p=0.17)和深层内膜(138%;p=0.05)中的 NPR-C 表达增加。在浅层内膜,NPR-C 的表达明显与血管平滑肌细胞(VSMC)和巨噬细胞共定位。在浅层内膜斑肩和斑盖区域,NPR-C的表达强度也较高,并与动脉粥样斑块和纤维粥样斑块易损斑块区域明显相关(β=1.04,95% CI=0.46,1.64):这些研究结果表明,NPR-C在晚期颈动脉斑块内膜中表达明显。此外,NPR-C 在易损颈动脉斑块内膜区域的表达量更高,并与晚期疾病的特征相关。我们的研究结果表明,NPR-C 可作为晚期颈动脉闭塞性疾病患者颈动脉斑块脆弱性和进展的潜在生物标志物。
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Natriuretic Peptide Receptor-C is Up-Regulated in the Intima of Advanced Carotid Artery Atherosclerosis.

Objective: Natriuretic peptide receptor-C (NPR-C/NPR-3) is a cell surface protein involved in vascular remodelling that is up-regulated in atherosclerosis. NPR-C expression has not been well characterized in human carotid artery occlusive lesions. We hypothesized that NPR-C expression correlates with intimal features of vulnerable atherosclerotic carotid artery plaque.

Methods: To test this hypothesis, we evaluated NPR-C expression by immunohistochemistry (IHC) in carotid endarterectomy (CEA) specimens isolated from 18 patients. The grade, location, and co-localization of NPR-C in CEA specimens were evaluated using two tissue analysis techniques.

Results: Relative to minimally diseased CEA specimens, we observed avid NPR-C tissue staining in the intima of maximally diseased CEA specimens (65%; p=0.06). Specifically, maximally diseased CEA specimens demonstrated increased NPR-C expression in the superficial intima (61%, p=0.17), and deep intima (138% increase; p=0.05). In the superficial intima, NPR-C expression significantly co-localized with vascular smooth muscle cells (VSMCs) and macrophages. The intensity of NPR-C expression was also higher in the superficial intima plaque shoulder and cap regions, and significantly correlated with atheroma and fibroatheroma vulnerable plaque regions (β=1.04, 95% CI=0.46, 1.64).

Conclusion: These findings demonstrate significant NPR-C expression in the intima of advanced carotid artery plaques. Furthermore, NPR-C expression was higher in vulnerable carotid plaque intimal regions, and correlate with features of advanced disease. Our findings suggest that NPR-C may serve as a potential biomarker for carotid plaque vulnerability and progression, in patients with advanced carotid artery occlusive disease.

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