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动脉粥样硬化斑块中细胞凋亡及其相关基因的表达 被引量:4

Apoptosis and expression of its related genes in human atherosclerotic plaques
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摘要 目的 :研究动脉粥样硬化 (AS)病灶中细胞凋亡的发生情况及其相关基因的表达情况 ,探讨细胞凋亡与bcl 2、p5 3、C myc基因表达的内在联系。方法 :选择因AS住院手术患者 2 0例作为研究对象〔其中男 17例 ,女 3例 ,平均年龄 (6 6 .8± 9.86 )岁 ,主要取患者的股动脉〕 ,及因意外伤害手术患者的 10例〔其中男 8例 ,女 2例 ,平均年龄 (5 1.6± 11.97)岁〕作为正常对照。采用末端脱氧核苷酸转移酶介导的dUTP缺口末端标记 (TUNEL)技术检测两组动脉标本的细胞凋亡情况 ,采用免疫组化的方法检测bcl 2、p5 3及C myc基因的表达情况 ,应用透射电镜进行两组动脉标本的细胞形态学观察。结果 :AS病灶中 ,细胞凋亡的发生率明显高于正常对照血管 (P <0 .0 1) ,bcl 2蛋白的表达明显降低 ,p5 3蛋白及C myc蛋白的表达明显升高 (P <0 .0 1) ;透射电镜证实AS病灶中有大量的平滑肌细胞发生凋亡。结论 :细胞凋亡是AS病灶中细胞死亡的一种主要形式 ,bcl 2、p5 3及C myc基因的表达可能对细胞凋亡的发生起重要的调控作用。 Objective:To study apoptosis and expressions of protooncogenes bcl-2, p53 and C-myc of cells in human atherosclerotic (AS) plaques.Method:Arterial specimens were derived from 20 patients operated as arteriosclerosis and 10 victims. Cell apoptosis was in site detected with the terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) and transmission electron microscope. The expressions of protooncogenes bcl-2, p53 and C-myc was detected with immunohistochemistry.Result:Compared with normal arteries, more cells were found to be positively stained with TUNEL in AS plaques (P< 0.01). Lots of smooth muscle cells in AS plaques were found to be apoptosis with electron microscope. The expression of protooncogene bcl-2 was markedly decreased in AS plaques, but the expressions of p53 and c-myc was markedly increased (P< 0.01).Conclusion:Apoptosis is a main type of cell death in human AS plaques. The expressions of protooncogenes bcl-2, p53 and C-myc may play an important role in regulating the apoptosis.
出处 《临床心血管病杂志》 CAS CSCD 北大核心 2004年第8期451-454,共4页 Journal of Clinical Cardiology
基金 福建省卫生厅资助 (No :2 0 0 0 0 6 )
关键词 动脉粥样硬化 细胞凋亡 基因 BCL 2 基因 P53 Atherosclerosis Apoptosis Gene, bcl 2 Gene, p53
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  • 1Isner J M, Kearney M, Bortman S, et al. Apoptosis in human atherosclerosis and restenosis. Circulation,1995, 91:2703-2711.
  • 2Bjorkerud S, Bjorkerud B. Apoptosis is abundant in human atherosclerotic lesions, especially in inflammatory cells (macrophages and T cells), and may contribute to the accumulation of gruel and plaque instability. Am J Pathol, 1996, 149:367-380.
  • 3Han D K, Haudenschild C C, Hong M K, et al. Evidence for apoptosis in human atherogenesis and in a rat vascular injury model. Am J Pathol, 1995, 147:267-277.
  • 4Harada K, Chen Z, Ishibashi S, et al. Apoptotic cell death in atherosclerotic plaques of hyperlipidemic knockout mice. Atherosclerosis, 1997, 135:235-239.
  • 5Davies M J. Apoptosis in cardiovascular disease.Heart, 1997, 77:498-501.
  • 6Rekhter M D. Collagen synthesis in atherosclerosis: too much and not enough. Cardiovasc Res, 1999, 41:376-384.
  • 7Kockx M M, Muhring J, Bortier H, et al. Biotin-or digoxigenin-conjugated nucleotides bind to matrix vesicles in atherosclerotic plaques. Am J Pathol, 1996,148:1771-1777.
  • 8Flynn P D, Byrne C D, Baglin T P, et al. Thrombin generation by apoptotic vascular smooth muscle cells.Blood, 1997, 89:4378-4384.
  • 9Bennett M R, Evan G I, Newby A C. Deregulated expression of the c-myc oncogene abolishes inhibition of proliferation of rat vascular smooth muscle cells by serum reduction, interferon-gamma, heparin, and cyclic nucleotide analogues and induces apoptosis.
  • 10Bennett M R, Littlewood T D, Schwartz S M, et al.Increased sensitivity of human vascular smooth muscle cells from atherosclerotic plaques to p53-mediated apoptosis. Circ Res, 1997, 81:591-599.

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