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人类动脉粥样硬化性颈动脉斑块中的组织标志物。

Tissue markers in human atherosclerotic carotid artery plaque.

作者信息

Moller Michelle J, Qin Zhenyu, Toursarkissian Boulos

机构信息

Division of Vascular Surgery, Department of Surgery, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA.

出版信息

Ann Vasc Surg. 2012 Nov;26(8):1160-5. doi: 10.1016/j.avsg.2012.06.008.

Abstract

Carotid artery stenosis predisposes to thrombo-embolization and stroke. Established tissue markers such as osteopontin, nitric oxide synthases, myeloperoxidases, and matrix metalloproteinases have been examined within stenotic plaques and their impact upon plaque stability discussed. However, a new generation of tissue markers is being discovered, and their role in atherosclerotic development and plaque stability is being debated. Prostaglandin synthase, 15-lipoxygenase-2, myeloid-related proteins 8 and 14, and protease nexin-1 have recently been shown to correlate with carotid artery atherosclerosis. These proteins highlight new areas of interest in the role of macrophages in atherosclerotic development, plaque formation, and rupture. Additionally, these new molecules raise the possibility of new screening and treatment techniques.

摘要

颈动脉狭窄易引发血栓栓塞和中风。诸如骨桥蛋白、一氧化氮合酶、髓过氧化物酶和基质金属蛋白酶等已确立的组织标志物已在狭窄斑块中进行了检测,并讨论了它们对斑块稳定性的影响。然而,新一代组织标志物正在被发现,它们在动脉粥样硬化发展和斑块稳定性中的作用也在被争论。前列腺素合酶、15-脂氧合酶-2、髓样相关蛋白8和14以及蛋白酶nexin-1最近已被证明与颈动脉粥样硬化相关。这些蛋白质凸显了巨噬细胞在动脉粥样硬化发展、斑块形成和破裂中的作用这一令人感兴趣的新领域。此外,这些新分子增加了新的筛查和治疗技术的可能性。

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