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首页> 外文期刊>Cell biology international. >Inhibition of new vessel growth in mouse model of laser-induced choroidal neovascularization by adiponectin peptide II.
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Inhibition of new vessel growth in mouse model of laser-induced choroidal neovascularization by adiponectin peptide II.

机译:脂联素肽Ⅱ抑制小鼠激光诱导的脉络膜新血管形成模型中新血管的生长。

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We have investigated the effect of adiponectin (APN) peptide II on new vessel growth in mouse model of choroidal neovascularization (CNV) or wet type age-related macular degeneration (AMD). Mice were injected intraperitoneally with APN peptide II, control peptide, or PBS on day 1-7 or day 5-14. APN, AdipoR1, PCNA, and VEGF localization was investigated using confocal microscopy, immunohistochemistry, and RT-PCR. APN peptide II decreased the relative area of FITC-dextran perfused vessels by 4-fold, PCNA expression by 3-fold, and the number of PCNA stained HUVEC and MAVEC cells by 38 and 46%, respectively. We concluded that APN peptide II inhibits CNV size on days 7 and 14 by inhibiting the proliferation of endothelial cells in vivo and in vitro. APN peptide II may have therapeutic potential to inhibit CNV or wet AMD.
机译:我们已经研究了脂联素(APN)肽II对脉络膜新生血管(CNV)或湿性年龄相关性黄斑变性(AMD)小鼠模型中新血管生长的影响。在第1-7天或第5-14天向小鼠腹膜内注射APN肽II,对照肽或PBS。使用共聚焦显微镜,免疫组织化学和RT-PCR研究了APN,AdipoR1,PCNA和VEGF的定位。 APN肽II使FITC-葡聚糖灌注血管的相对面积减少了4倍,PCNA表达减少了3倍,PCNA染色的HUVEC和MAVEC细胞的数量分别减少了38%和46%。我们得出的结论是,APN肽II通过在体内和体外抑制内皮细胞的增殖而在第7天和第14天抑制CNV大小。 APN肽II可能具有抑制CNV或湿性AMD的治疗潜力。

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