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首页> 外文期刊>World Journal of Gastroenterology >Effects of adrenomedullin gene overexpression on biological behavior of hepatic stellate cells.
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Effects of adrenomedullin gene overexpression on biological behavior of hepatic stellate cells.

机译:肾上腺髓质素基因过表达对肝星状细胞生物学行为的影响。

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AIM: To investigate the effects of adrenomedullin (AM) gene overexpression on the biological characteristics of human hepatic stellate cells (hHSCs) by stable transfection. METHODS: hHSCs which express low basal levels of AM were stably transfected with an expression construct containing rat AM gene or with an empty expression vector. Expression of AM in hHSCs was determined by reverse transcription (RT)-polymerase chain reaction (PCR) and radioimmunoassay (RIA). Cell proliferation was evaluated by 5-bromo-2'-deoxyuridine (BrdU) incorporation and immunocytochemistry. RT-PCR and Western blot were used to test the expression of procollagen types I and III. Protein expressions of interstitial collagenase (MMP-1), gelatinase (MMP-2) and tissue inhibitors of matrix metalloproteinases-2 (TIMP-2) were assessed by Western blot. RESULTS: Two cell clones (A-2, A-8) transfected with the AM gene expressed higher levels of AM mRNA (non-transfected group: 0.86+/-0.11, empty vector group: 1.01+/-0.11, A-2 clone group: 1.44+/-0.08 and A-8 clone group: 1.36+/-0.05) and protein (12.31+/-0.17, 12.35+/-0.12, 12.56+/-0.06 and 12.62+/-0.07) (P<0.05). AM gene overexpression had inhibitory effects on cell proliferation of hHSCs (29.6%, 30.9%, 18.9% and 21.8%, respectively. P<0.05) and expression of procollagen type I (0.58+/-0.1, 0.48+/-0.11, 0.3+/-0.06 and 0.31+/-0.07 at mRNA level) (0.27+/-0.07, 0.3+/-0.06, 0.14+/-0.05 and 0.13+/-0.05 at protein level) (P<0.05) and procollagen type III (0.17+/-0.04, 0.15+/-0.03, 0.1+/-0.02 and 0.09+/-0.02 at mRNA level) (0.22+/-0.04, 0.2+/-0.03, 0.11+/-0.04 and 0.13+/-0.03 at protein level) (P<0.05). Compared with cells non-transfected (TIMP2: 2.77+/-0.03, MMP-2: 0.5+/-0.04, MMP-1: 0.49+/-0.07) and transfected with empty vector (TIMP2: 2.79+/-0.04, MMP-2: 0.48+/-0.03, MMP-1: 0.45+/-0.09), these two clones had lower expression levels of TIMP2(A-2 clone group: 2.7+/-0.02 and A-8 clone group: 2.71+/-0.02) (P<0.05) and MMP-2(A-2 clone group: 0.15+/-0.05 and A-8 clone group: 0.13+/-0.04) (P<0.05) but displayed a higher expression level of MMP-1(A-2 clone group: 0.68+/-0.06 and A-8 clone group: 0.81+/-0.09) (P<0.05). CONCLUSION: AM gene exerts negative influence to some extent on hHSCs by inhibiting proliferation and production of extracellular matrix (ECM) in addition to inducing MMP-1 expression.
机译:目的:通过稳定转染研究肾上腺髓质素(AM)基因过表达对人肝星状细胞(hHSCs)生物学特性的影响。方法:用含有大鼠AM基因的表达构建体或空表达载体稳定转染表达低基础水平AM的hHSC。通过逆转录(RT)-聚合酶链反应(PCR)和放射免疫分析(RIA)确定hHSC中AM的表达。通过5-溴-2'-脱氧尿苷(BrdU)掺入和免疫细胞化学评估细胞增殖。用RT-PCR和Western blot检测I和III型胶原原的表达。通过蛋白质印迹法评估间质胶原酶(MMP-1),明胶酶(MMP-2)和基质金属蛋白酶-2(TIMP-2)的组织抑制剂的蛋白表达。结果:转染AM基因的两个细胞克隆(A-2,A-8)表达更高水平的AM mRNA(未转染组:0.86 +/- 0.11,空载体组:1.01 +/- 0.11,A-2克隆组:1.44 +/- 0.08和A-8克隆组:1.36 +/- 0.05)和蛋白质(12.31 +/- 0.17、12.35 +/- 0.12、12.56 +/- 0.06和12.62 +/- 0.07)(P <0.05)。 AM基因过表达对hHSCs的细胞增殖具有抑制作用(分别为29.6%,30.9%,18.9%和21.8%。P<0.05)和I型前胶原的表达(0.58 +/- 0.1、0.48 +/- 0.11、0.3)。在mRNA水平上为+/- 0.06和0.31 +/- 0.07)(在蛋白水平上为0.27 +/- 0.07、0.3 +/- 0.06、0.14 +/- 0.05和0.13 +/- 0.05)(P <0.05)和前胶原类型III(在mRNA水平上为0.17 +/- 0.04、0.15 +/- 0.03、0.1 +/- 0.02和0.09 +/- 0.02)(0.22 +/- 0.04、0.2 +/- 0.03、0.11 +/- 0.04和0.13+在蛋白质水平上为--0.03)(P <0.05)。与未转染的细胞(TIMP2:2.77 +/- 0.03,MMP-2:0.5 +/- 0.04,MMP-1:0.49 +/- 0.07)并用空载体转染的细胞(TIMP2:2.79 +/- 0.04,MMP -2:0.48 +/- 0.03,MMP-1:0.45 +/- 0.09),这两个克隆的TIMP2表达水平较低(A-2克隆组:2.7 +/- 0.02,A-8克隆组:2.71+ /-0.02)(P <0.05)和MMP-2(A-2克隆组:0.15 +/- 0.05和A-8克隆组:0.13 +/- 0.04)(P <0.05),但表达水平较高MMP-1(A-2克隆组:0.68 +/- 0.06和A-8克隆组:0.81 +/- 0.09)(P <0.05)。结论:AM基因除了诱导MMP-1表达外,还通过抑制细胞外基质(ECM)的增殖和产生,在一定程度上对hHSCs产生负面影响。

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