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缺氧在人垂体腺瘤细胞系中诱导细胞侵袭增加。

Elevated cell invasion is induced by hypoxia in a human pituitary adenoma cell line.

作者信息

Yoshida Daizo, Teramoto Akira

机构信息

Department of Neurosurgery, Nippon Medical School, Nippon Medical School, Tokyo, Japan.

出版信息

Cell Adh Migr. 2007 Jan-Mar;1(1):43-51. Epub 2007 Jan 27.

Abstract

Pituitary adenoma tissues are hypovascular, and have a lower partial oxygen pressure compared with neighboring normal organs. In this study, we investigated whether hypoxia influences the cell invasiveness of the human pituitary adenoma cell line, HP-75. HP-75 cells were exposed to hypoxic (1-10% oxygen) or normoxic (21% oxygen) conditions for 24 hours. Gelatin and reverse zymogram assays were used to determine the enzyme activities of matrix metalloproteinases (MMP) and tissue inhibitor of metalloproteinases (TIMP). Cell adhesion and Matrigel cell invasion were examined with a Boiden chamber. Finally, the mRNA gene expression profiles of cells exposed to hypoxia or normoxia were examined by cDNA microarray and confirmed with real-time RT-PCR and flow cytometry. The gelatin and reverse zymograms revealed that the activities of MMP and TIMP were not significantly altered by hypoxia. Matrigel cell invasion and cell adhesion to Matrigel or collagen type IV were increased by hypoxia (3.8- and 4.8-fold, respectively). The cDNA microarray analysis revealed that laminin beta2 chain mRNA was specifically up-regulated under hypoxic conditions (4.96-fold). Finally, real-time RT-PCR and flow cytometry verified the elevated expression of laminin beta2 chain at the mRNA and protein levels under hypoxic conditions. RNA interference with siRNA targeting laminin beta2 inhibited Matrigel invasion and adhesion to collagen type IV in a dose-dependent manner. Collectively, these results suggested that hypoxia (1% oxygen) enhanced the cell invasion properties of a pituitary adenoma cell line in association with elevated expression of laminin beta2 and enhanced binding to collagen type IV.

摘要

垂体腺瘤组织血管较少,与邻近正常器官相比局部氧分压较低。在本研究中,我们调查了缺氧是否会影响人垂体腺瘤细胞系HP - 75的细胞侵袭性。将HP - 75细胞置于低氧(1 - 10%氧气)或常氧(21%氧气)条件下24小时。采用明胶和反向酶谱分析来测定基质金属蛋白酶(MMP)和金属蛋白酶组织抑制剂(TIMP)的酶活性。用Boyden小室检测细胞黏附和基质胶细胞侵袭情况。最后,通过cDNA微阵列检测暴露于低氧或常氧条件下细胞的mRNA基因表达谱,并通过实时RT - PCR和流式细胞术进行验证。明胶和反向酶谱显示,缺氧并未显著改变MMP和TIMP的活性。缺氧使基质胶细胞侵袭以及细胞与基质胶或IV型胶原的黏附增加(分别增加3.8倍和4.8倍)。cDNA微阵列分析显示,层粘连蛋白β2链mRNA在低氧条件下特异性上调(4.96倍)。最后,实时RT - PCR和流式细胞术验证了低氧条件下层粘连蛋白β2链在mRNA和蛋白质水平的表达升高。用靶向层粘连蛋白β2的小干扰RNA(siRNA)进行RNA干扰,以剂量依赖方式抑制基质胶侵袭和与IV型胶原的黏附。总的来说,这些结果表明,缺氧(1%氧气)与层粘连蛋白β2表达升高及与IV型胶原结合增强相关,增强了垂体腺瘤细胞系的细胞侵袭特性。

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