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MDCK细胞外基质对HK-2细胞的增殖和迁移的影响
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  • 英文篇名:Effects of MDCK extracellular matrix on the proliferation and migration of HK-2 cells
  • 作者:袁育珺 ; 杨秀玲 ; 胡志坚 ; 汪渊
  • 英文作者:Yuan Yujun;Yang Xiuling;Hu Zhijian;Clinical Laboratory,The Affiliated Hospital of Jiujiang University;Hospital Sense,The Affiliated Hospital of Jiujiang University;Dept of Molecular Biology and Biochemistry,Anhui Medical University;
  • 关键词:细胞外基质 ; HK-2 ; 整合素 ; 增殖 ; 迁移
  • 英文关键词:extracellular matrix;;HK-2;;integrins;;proliferation;;migration
  • 中文刊名:YIKE
  • 英文刊名:Acta Universitatis Medicinalis Anhui
  • 机构:江西省九江学院附属医院检验科;江西省九江学院附属医院院感科;安徽医科大学分子生物学实验室生物化学教研室安徽省/省部共建教育部重要遗传病基因资源利用重点实验室;
  • 出版日期:2019-01-11 14:06
  • 出版单位:安徽医科大学学报
  • 年:2019
  • 期:v.54
  • 基金:江西省卫生计生委科技计划项目(编号:20181141)
  • 语种:中文;
  • 页:YIKE201902011
  • 页数:4
  • CN:02
  • ISSN:34-1065/R
  • 分类号:52-55
摘要
目的研究MDCK细胞外基质对HK-2细胞的增殖和迁移的影响。方法用氨水制备MDCK细胞外间质,并且作为HK-2细胞培养基础,随机分为正常对照组和细胞外基质组。用酸性磷酸酶、细胞划痕实验观察细胞的增殖和迁移状况;细胞免疫荧光和Westen blot分析整合素α3和α6蛋白的表达变化。结果与正常对照组比较,MDCK细胞外基质能明显促进HK-2细胞的体外增殖和迁移,整合素α3和α6表达增加(P <0. 05)。结论 MDCK细胞外基质可促进体外培养的HK-2细胞的增殖和迁移。
        Objective To study the effects of extracellular matrix on the proliferation and migration of HK-2 cells.Methods The MDCK extracellular matrix was used as the basis for the culture of HK-2 cells and randomly divided into normal control group and extracellular matrix group. The condition of cell proliferation and migration was observed with acid phosphatase and cell scratches; the expression of integrin α3 and α6 protein was analyzed by immunofluorescence and Western blot. Results Compared with normal group,MDCK extracellular matrix significantly promoted the proliferation and migration of HK-2 cells in vitro,and increased the expression of integrin α3 andα6(P < 0. 05). Conclution MDCK extracellular matrix could promote the proliferation and migration of HK-2 cells cultured in vitro.
引文
[1] Humphries M J. Integrin structure[J]. Biochem Soc Trans,2000,28(4):311-39.
    [2] Takahashi T,Friedmacher F,Zimmer J,et al. Decreased expression of integrin subunitsα3,α6,andα8 in the branching airway mesenchyme of nitrofen-induced hypoplastic lungs[J]. Eur J Pediatr Surq,2018,28(1):109-14.
    [3] Liao H D,Mao Y,Ying Y G. The involvement of the laminin-integrinα7β1 signaling pathway in mechanical ventilation-induced pulmonary fibrosis[J]. J Thorac Dic,2017,9(10):3961-72.
    [4] Schütte K,Schulz C,Link A,et al. Current biomarkers for hepatocellular carcinoma:surveillance,diagnosis and prediction of prognosis[J]. World J Hepatol,2015,7(2):139-49.
    [5]汪渊,桂淑玉. 804G细胞外间质对体外培养牛角膜内皮细胞增殖的影响[J].中国药理学通报,1998,14(4):348-50.
    [6]张金明,崔永言,徐路生.兔脱细胞尿道基质制备的可行性[J].中国临床康复,2005,9(42):48-9.
    [7]袁育珺,段惠芳,胡志坚,等.高糖诱导人肾近曲小管上皮细胞凋亡及其调控机制[J].安徽医科大学学报,2016,51(4):497-501.
    [8] De Nicola L,Gabbai F B,Liberti M E,et al. Sodium/glucose cotransporter2 inhibitors and prevention of diabetic nephropathy:targeting the renal tubule in diabetes[J]. Am J Kidney Dis,2014,64(1):16-24.
    [9] Guo K,Lu J,Huang Y,et al. Protective role of PGC-1αin diabetic nephropathy is associated with the inhibition of ROS through mitochondrial dynamic remodeling[J]. PLo S One,2015,10(4):e0125176.
    [10]胡红林,王共先.肾缺血再灌注损伤中细胞凋亡和氧化应激[J].中国现代医学杂志,2010,20(15):2279-83.
    [11] Chan L S,Wang X S,Lapiere J C,et al. A newly identified 105-kD lower lamina lucida autoantigen is an acidic protein distinct from the 105-kD gamma 2 chain of laminin-5[J]. J Invet Dermatol,1995,105(1):75-9.
    [12] Campbell I D,Humphries M J. Integrin structure,activation,and interactions[J]. Cold Spring Harb Perspect Biol,2011,3(3):a004994.
    [13]李雪映,孙小然,张宏权.整合素相关微环境调控肿瘤转移[J].生物化学与生物物理进展,2017,44(8):672-7.
    [14] Caswell P T,Vadrevu S,Norman J C. Integrins:Masters and slaves of endocytic transport[J]. Nat Rev Mol Cell Biol,2009,10(12):843-53.
    [15] Lonqmate W M,Lyons S P,De Freest L,et al. Opposing roles of epidermal integrinsα3β1 andα9β1 in Regulation of m TLD/BMP-1-mediated laminin-γ2 processing during wound healing[J]. J Invest Dermatol,2018,38(2):444-51.

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