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肿瘤条件培养基调节人脐静脉内皮细胞的增殖、黏附和迁移

[Tumor conditioned medium regulates the proliferation, adhesion and migration of human umbilical vein endothelial cells].

作者信息

Zhang Ting, Jiang Chun-Lei

机构信息

Department of Nautical Medicine, Second Military Medical University, Shanghai, China.

出版信息

Sheng Li Xue Bao. 2011 Jun 25;63(3):256-60.

Abstract

The aim of the present study was to investigate the effects of tumor conditioned medium (TCM) on the proliferation, adhesion and migration of human umbilical vein endothelial cell (HUVEC). Cells were divided into control group, TCM stock solution group, TCM monodilution group and TCM didilution group (n = 6), and MTT assay was used to determine endothelial cells proliferation level after being stimulated with TCM for 24 h. Coating culture dishes with Fn was used to detect the adhesion ability of endothelial cells to basement membrane in control group and TCM stock solution group (n = 6). Wound closure model was used to test the migration ability of endothelial cells in control group and TCM stock solution group at 12 h and 24 h (n = 6). The results showed that TCM at different concentrations influenced proliferation of endothelial cells in distinct degree. Compared to the control group (absorbance value: 0.58 ± 0.04), the stock solution had no effect on proliferation of endothelial cells (absorbance value: 0.55 ± 0.01). However, the TCM monodilution and TCM didilution enhanced the proliferation of endothelial cells significantly (absorbance value: 0.66 ± 0.03, P < 0.01 and 0.70 ± 0.02, P < 0.001 separately). TCM downregulated the adhesion of endothelial cells to basement membrane. Moreover, compared to the migration distance of control group at 12 h and 24 h [(14.05 ± 6.25) µm and (48.75 ± 16.37) µm separately], TCM upregulated the basement membrane migration [(68.25 ± 26.20) µm and (119.70 ± 34.90) µm at 12 h and 24 h, both P < 0.05 separately]. These results suggest that TCM downregulates the adhesion ability of endothelial cells and upregulates their migration ability, and thus facilitates tumor metastasis.

摘要

本研究旨在探讨肿瘤条件培养基(TCM)对人脐静脉内皮细胞(HUVEC)增殖、黏附和迁移的影响。将细胞分为对照组、TCM原液组、TCM单倍稀释组和TCM双倍稀释组(n = 6),采用MTT法检测TCM刺激24 h后内皮细胞的增殖水平。用纤连蛋白(Fn)包被培养皿,检测对照组和TCM原液组(n = 6)中内皮细胞与基底膜的黏附能力。采用划痕愈合模型检测对照组和TCM原液组在12 h和24 h时内皮细胞的迁移能力(n = 6)。结果显示,不同浓度的TCM对内皮细胞增殖有不同程度的影响。与对照组(吸光度值:0.58±0.04)相比,原液对内皮细胞增殖无影响(吸光度值:0.55±0.01)。然而,TCM单倍稀释组和TCM双倍稀释组显著增强了内皮细胞的增殖(吸光度值分别为0.66±0.03,P < 0.01和0.70±0.02,P < 0.001)。TCM下调了内皮细胞与基底膜的黏附。此外,与对照组在12 h和24 h时的迁移距离[分别为(14.05±6.25) µm和(48.75±16.37) µm]相比,TCM上调了基底膜迁移能力[在12 h和24 h时分别为(68.25±26.20) µm和(119.70±34.90) µm,P均< 0.05]。这些结果表明,TCM下调内皮细胞的黏附能力,上调其迁移能力,从而促进肿瘤转移。

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