Department of Anatomy, School of Medicine, University of Patras, 26500, Rio, Patras, Greece.
Department of Anatomy, School of Medicine, University of Patras, 26500, Rio, Patras, Greece.
Cardiovasc Pathol. 2014 May-Jun;23(3):131-8. doi: 10.1016/j.carpath.2014.02.003. Epub 2014 Feb 25.
Adipose tissue is considered an endocrine organ, producing bioactive peptides, called adipokines. Adipokines produced by periadventitial fat have been implicated in the pathogenesis of vascular disease, including atherosclerosis. Adiponectin has established antiatherogenic actions, while the role of T-cadherin as an adiponectin receptor is not fully elucidated. The apelinergic system, consisting of apelin and its APJ receptor, is a mediator of various cardiovascular functions and may also be involved in the atherosclerotic process. We investigated the protein expression of adiponectin, T-cadherin, apelin and APJ in human aortas, coronary vessels, and the respective periadventitial adipose tissue and correlated their expression with the presence of atherosclerosis and clinical parameters.
Immunohistochemistry for adiponectin, T-cadherin, apelin, and APJ was performed on human aortic and coronary artery samples including the periadventitial adipose tissue. Aortic and coronary atherosclerotic lesions were assessed using the american heart association (AHA) classification.
Adiponectin immunostaining, of varied intensity, was detected only in adipocytes, while T-cadherin was localized to vascular smooth muscle cells (VSMCs) and endothelial cells. Apelin immunostaining was detected in adipocytes, VSMCs, endothelial cells, and foam cells in atherosclerotic lesions, while APJ was found in VSMCs and endothelia. Periadventitial adiponectin and VSMC T-cadherin expression were negatively correlated with atherosclerosis in both sites, as was VSMC apelin expression. Several other - depot specific - associations were observed.
Our results suggest a possible role for T-cadherin as a mediator of antiatherogenic adiponectin actions, while they support the putative antiatherogenic profile for apelin and its APJ receptor in human arteries. Further research is absolutely necessary to confirm these notions.
Periadventitial adipose tissue adipokines are implicated in vascular physiology and pathology. Adiponectin/T-cadherin and apelin/APJ immunoreactivity is detected in human aortas and coronary arteries. Adiponectin/T-cadherin and apelin/APJ expression patterns were found to be inversely associated with human aortic and coronary atherosclerosis.
脂肪组织被认为是一种内分泌器官,可产生生物活性肽,称为脂肪因子。血管周围脂肪产生的脂肪因子已被牵连到血管疾病的发病机制中,包括动脉粥样硬化。脂联素具有明确的抗动脉粥样硬化作用,而 T-钙黏蛋白作为脂联素受体的作用尚未完全阐明。由 Apelin 和其 APJ 受体组成的 Apelin 能系统是各种心血管功能的介质,也可能参与动脉粥样硬化过程。我们研究了人主动脉、冠状动脉及其相应血管周围脂肪组织中脂联素、T-钙黏蛋白、Apelin 和 APJ 的蛋白表达,并将其表达与动脉粥样硬化的存在及其临床参数相关联。
采用免疫组织化学方法检测人主动脉和冠状动脉样本中的脂联素、T-钙黏蛋白、Apelin 和 APJ,包括血管周围脂肪组织。采用美国心脏协会(AHA)分类法评估主动脉和冠状动脉粥样硬化病变。
脂联素免疫染色强度不同,仅在脂肪细胞中检测到,而 T-钙黏蛋白定位于血管平滑肌细胞(VSMCs)和内皮细胞。Apelin 免疫染色在动脉粥样硬化病变中的脂肪细胞、VSMCs、内皮细胞和泡沫细胞中检测到,而 APJ 则在 VSMCs 和内皮细胞中发现。在两个部位,血管周围脂肪组织中的脂联素和 VSMC T-钙黏蛋白表达与动脉粥样硬化呈负相关,VSMC 中的 Apelin 表达也是如此。还观察到一些其他的“特定脂肪组织库”的相关性。
我们的研究结果表明,T-钙黏蛋白可能作为抗动脉粥样硬化脂联素作用的介导物,而支持 Apelin 及其 APJ 受体在人类动脉中的抗动脉粥样硬化作用。需要进一步的研究来证实这些观点。
血管周围脂肪组织的脂肪因子与血管生理学和病理学有关。在人主动脉和冠状动脉中检测到脂联素/T-钙黏蛋白和 Apelin/APJ 免疫反应性。发现脂联素/T-钙黏蛋白和 Apelin/APJ 的表达模式与人类主动脉和冠状动脉粥样硬化呈负相关。