Hinton Ayana, Sennoune Souad R, Bond Sarah, Fang Min, Reuveni Moshe, Sahagian G Gary, Jay Daniel, Martinez-Zaguilan Raul, Forgac Michael
From the Department of Physiology, Tufts University School of Medicine, Boston, Massachusetts 02111.
Department of Cell Physiology and Molecular Biophysics, Texas Tech University, Lubbock, Texas 79430.
J Biol Chem. 2009 Jun 12;284(24):16400-16408. doi: 10.1074/jbc.M901201200. Epub 2009 Apr 14.
It has previously been shown that highly invasive MDA-MB231 human breast cancer cells express vacuolar proton-translocating ATPase (V-ATPases) at the cell surface, whereas the poorly invasive MCF7 cell line does not. Bafilomycin, a specific V-ATPase inhibitor, reduces the in vitro invasion of MB231 cells but not MCF7 cells. Targeting of V-ATPases to different cellular membranes is controlled by isoforms of subunit a. mRNA levels for a subunit isoforms were measured in MB231 and MCF7 cells using quantitative reverse transcription-PCR. The results show that although all four isoforms are detectable in both cell types, levels of a3 and a4 are much higher in MB231 than in MCF7 cells. Isoform-specific small interfering RNAs (siRNA) were employed to selectively reduce mRNA levels for each isoform in MB231 cells. V-ATPase function was assessed using the fluorescent indicators SNARF-1 and pyranine to monitor the pH of the cytosol and endosomal/lysosomal compartments, respectively. Cytosolic pH was decreased only on knockdown of a3, whereas endosome/lysosome pH was increased on knockdown of a1, a2, and a3. Treatment of cells with siRNA to a4 did not affect either cytosolic or endosome/lysosome pH. Measurement of invasion using an in vitro transwell assay revealed that siRNAs to both a3 and a4 significantly inhibited invasion of MB231 cells. Immunofluorescence staining of MB231 cells for V-ATPase distribution revealed extensive intracellular staining, with plasma membrane staining observed in approximately 18% of cells. Knockdown of a4 had the greatest effect on plasma membrane staining, leading to a 32% reduction. These results suggest that the a4 isoform may be responsible for targeting V-ATPases to the plasma membrane of MB231 cells and that cell surface V-ATPases play a significant role in invasion. However, other V-ATPases affecting the pH of the cytosol and intracellular compartments, particularly those containing a3, are also involved in invasion.
先前的研究表明,高侵袭性的MDA-MB231人乳腺癌细胞在细胞表面表达液泡质子转运ATP酶(V-ATP酶),而低侵袭性的MCF7细胞系则不表达。巴弗洛霉素是一种特异性V-ATP酶抑制剂,它能降低MB231细胞的体外侵袭能力,但对MCF7细胞没有影响。V-ATP酶靶向不同细胞膜是由a亚基的同工型控制的。使用定量逆转录-PCR测量MB231和MCF7细胞中a亚基同工型的mRNA水平。结果表明,虽然在两种细胞类型中都能检测到所有四种同工型,但MB231细胞中a3和a4的水平远高于MCF7细胞。使用同工型特异性小干扰RNA(siRNA)选择性降低MB231细胞中每种同工型的mRNA水平。使用荧光指示剂SNARF-1和吡喃荧光素分别监测细胞质和内体/溶酶体区室的pH值,以评估V-ATP酶的功能。仅在敲低a3时细胞质pH值降低,而在敲低a1、a2和a3时内体/溶酶体pH值升高。用针对a4的siRNA处理细胞对细胞质或内体/溶酶体pH值均无影响。使用体外Transwell试验测量侵袭能力,结果显示针对a3和a4的siRNA均显著抑制MB231细胞的侵袭。对MB231细胞进行V-ATP酶分布的免疫荧光染色显示细胞内有广泛的染色,约18%的细胞观察到质膜染色。敲低a4对质膜染色的影响最大,导致质膜染色减少32%。这些结果表明,a4同工型可能负责将V-ATP酶靶向MB231细胞的质膜,并且细胞表面的V-ATP酶在侵袭中起重要作用。然而,其他影响细胞质和细胞内区室pH值的V-ATP酶,特别是那些含有a3的V-ATP酶,也参与了侵袭过程。