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人类巨细胞病毒感染对血管平滑肌细胞脂代谢相关基因表达的影响 被引量:4

The Influence of HCMV Infection on Expression of Genes Associated With Lipid Metabolism in Vascular Smooth Muscle Cells
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摘要 目的研究人类巨细胞病毒感染对体外培养血管平滑肌细胞脂代谢相关基因表达的影响,探讨该病毒致动脉粥样硬化(As)的机制。方法以1 MOI人类巨细胞病毒感染体外培养的血管平滑肌细胞,利用基因表达谱芯片技术检测细胞脂代谢相关基因的表达变化。结果人类巨细胞病毒感染血管平滑肌细胞后,细胞内与脂代谢有关的基因表达出现明显的异常,其中表达上调的基因主要有低密度脂蛋白受体相关蛋白10、11、12、极低密度脂蛋白受体、B型清道夫受体、HMG-CoA合成酶、HMG-CoA还原酶、酰基辅酶A∶胆固醇酰基转移酶及脂肪酶合成酶等基因;表达下调的主要有载脂蛋白A1、载脂蛋白M和载脂蛋白H等基因。结论人类巨细胞病毒感染可能通过改变血管平滑肌细胞脂代谢相关基因的表达而参与As的发病过程。 Objective To investigate the effect of human cytomegalovirus infection on expression of genes associated with lipid metabolism in vascular smooth muscle ceils cultured in vitro, and to clarify the possible mechanisms of atherosclero- sis induced by this virus. Methods The expression change of genes associated with lipid metabolism in vascular smooth muscle cells cultivated in vitro after human cytomegalovirus infection were scanned by gene expression profiling chip. Re- sults There was an obvious abnorm~ expression profile of genes associated with lipid metabolism in vascular smooth muscle cells after challenged with human cytomegalovirus, the main up-regulated genes were low density lipoprotein receptor-related protein,very low density lipoprotein receptor, scavenger receptor class B, HMG-CoA synthetase, HMG-CoA reductases, acyl- Coenzyme A:cholesterol acyltransferase,fatty acid synthase,and so on,while the main down-regulated genes were apolipopro- rein A-I (APOA1), apolipoprotein M (APOM) and apolipoprotein H (APOH). Conclusion The involvement of human cytomegalovirus in the pathogenesis of atherosclerosis may be by changing the expression level of lipid metabolism genes.
出处 《中南医学科学杂志》 CAS 2013年第1期17-20,共4页 Medical Science Journal of Central South China
基金 湖南省卫生厅科研基金(B2008-079) 湖南省自然科学基金重点项目(10JJ2012)
关键词 动脉粥样硬化 人类巨细胞病毒 脂代谢 基因表达谱芯片 血管平滑肌细胞 atherosclerosis human cytomegalovirus lipid metabolism gene expression profiling chip vascular smooth muscle cells
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  • 1曹碧茵,施建蓉,童瑶,邹军.心理应激动物模型的研制及其应用[J].中国行为医学科学,2005,14(2):191-192. 被引量:29
  • 2王淳本,宗义强,吴万生,冯友梅,邓耀祖,冯宗忱.两步超速离心法快速分离大量血浆极低密度脂蛋白及低密度脂蛋白[J].同济医科大学学报,1995,24(3):169-171. 被引量:92
  • 3姚磊,何作云,董解菊.巨细胞病毒感染对SMC脂质代谢的影响及反义寡核苷酸的调节作用[J].重庆医学,2006,35(18):1643-1644. 被引量:6
  • 4何平,成蓓,王洪星,戚本玲.格列本脲对泡沫细胞形成的影响[J].中国医院药学杂志,2007,27(3):312-315. 被引量:2
  • 5Smith JL,Rangaraj K,Simpson R,et al.Quantitative analysis of the expression of ACAT genes in human tissues by real-time PCR.J Lipid Res,2004,45:686-696.
  • 6Kalayoglu MV,Byme GI.Induction of macrophage foam cell formation by Chlamydia pneumaniae.J Infect Dis,1998,177:725-729.
  • 7Boblin PM,Dumornay W,Hammersehlag MR.Use of HEp-2 cells for improved isolation and passage of Chlamydia pneumoniae.J Clin Microbiol,1992,30:1968-1971.
  • 8Saikku P,Leinanen M,Mattila K,et al.Serological evidence of an association of a novel Chlamydia,TWAR,with chronic coronary heart disease and acute myocardial infarction.Lancet,1988,332:983-986.
  • 9Romano Carratelli C,Nuzzo I,Cozzolino D,et al.Relationship between Chlamydia pneumoniae infection,inflammatory markers,and coronary heart diseases.Int Immunopharmacol,2006,6:848-853.
  • 10Jiang SJ,Kuo CC,Berry MW,et al.Identification and characterization of Chlamydia pneumoniae-specifie proteins that activate tumor necrosis factor alpha production in RAW 264.7 murine macrophages.Infect lmmun,2008,76:1558-1564.

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  • 1Ozkan TB, Mistik R, Dikiei B, et al. Antiviraltherapy in neonatal cholestatie eytomegalovirus hepatitis [J]. BMC Gastroenterol, 2007, 7- 9.
  • 2Sabouri Ghannad M, Roshanaei G, Habibi H, et al. The assessment of affected factors on cytomegalovirus and rubella virus prevalence in females in Hamadan, Iran [J]. Aeta Med Iran, 2014, 2(4): 303-309.
  • 3Griffiths P, Baraniak I, Reeves M. The pathogenesis of human cytomegalovirus[J].JPathol, 2014, 235(2): 288-297.
  • 4A1-Ghamdi A. Role of herpes simplex virus-1, eytomegalovirus and Epstein-Barr virus in atherosclerosis [J]. Pak J Pharm Sci, 2012, 25(1): 89-97.
  • 5Weinstock-Guttman B, Horakova D, Zivadinov R, et al. Interactions of serum cholesterol with anti-herpesvirus responses affect disease progression in clinically isolated syndromes [J]. J Neuroimmunol, 2013, 263(1-2): 121-127.
  • 6Liu L, Tuo HZ, Wang RJ, et al. Human cytomegalovirus-IgM seropositivity is not associated with atherogenic alterations of lipid profiles and inflammatory status in isehemic stroke patients: a preliminary study [J]. Neurol Res, 2011, 33(5): 473-481.
  • 7Gudleski-O'Regan N, Greco TM, Cristea 1M, et al. Increased expression of LDL receptor-related protein 1 during human cytomegalovirus infection reduces virion cholesterol and infectivity [J]. CellHost Microbe, 2012, 12(1): 86-96.
  • 8Gredmark-Russ S, S6derberg-Naucl6r C. Dendritic cell biology in human cytomegalovirus infection and the clinical consequences for host immunity and pathology [J]. Virulence, 2012, 3(7) : 621-634.
  • 9Halary F, Amara A, Lortat-Jacob H, et al. Human cytomegalovirus binding to DC-SIGN is required for dendritic cell infection and target cell trans-infeefion [J]. Immunity, 2002, 17(5) : 653-664.
  • 10Haspot F, Lavault A, Sinzger C, et al. Human cytomegalovirus entry into dendritic cells occurs via a macropinocytosis-like pathway in a pH-independent and cholesterol-dependent manner [J]. PLoS One, 2012, 7(4): e34795.

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