Literature DB >> 19366680

Function of a subunit isoforms of the V-ATPase in pH homeostasis and in vitro invasion of MDA-MB231 human breast cancer cells.

Ayana Hinton1, Souad R Sennoune, Sarah Bond, Min Fang, Moshe Reuveni, G Gary Sahagian, Daniel Jay, Raul Martinez-Zaguilan, Michael Forgac.   

Abstract

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.

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Year:  2009        PMID: 19366680      PMCID: PMC2713521          DOI: 10.1074/jbc.M901201200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  35 in total

1.  Molecular cloning and expression of three isoforms of the 100-kDa a subunit of the mouse vacuolar proton-translocating ATPase.

Authors:  T Nishi; M Forgac
Journal:  J Biol Chem       Date:  2000-03-10       Impact factor: 5.157

2.  Overexpression of vacuolar ATPase 16-kDa subunit in 10T1/2 fibroblasts enhances invasion with concomitant induction of matrix metalloproteinase-2.

Authors:  S Kubota; Y Seyama
Journal:  Biochem Biophys Res Commun       Date:  2000-11-19       Impact factor: 3.575

3.  Yeast V-ATPase complexes containing different isoforms of the 100-kDa a-subunit differ in coupling efficiency and in vivo dissociation.

Authors:  S Kawasaki-Nishi; T Nishi; M Forgac
Journal:  J Biol Chem       Date:  2001-03-02       Impact factor: 5.157

4.  pH and drug resistance. II. Turnover of acidic vesicles and resistance to weakly basic chemotherapeutic drugs.

Authors:  N Raghunand; R Martínez-Zaguilán; S H Wright; R J Gillies
Journal:  Biochem Pharmacol       Date:  1999-05-01       Impact factor: 5.858

5.  pH and drug resistance. I. Functional expression of plasmalemmal V-type H+-ATPase in drug-resistant human breast carcinoma cell lines.

Authors:  R Martínez-Zaguilán; N Raghunand; R M Lynch; W Bellamy; G M Martinez; B Rojas; D Smith; W S Dalton; R J Gillies
Journal:  Biochem Pharmacol       Date:  1999-05-01       Impact factor: 5.858

6.  Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing.

Authors:  A N Smith; J Skaug; K A Choate; A Nayir; A Bakkaloglu; S Ozen; S A Hulton; S A Sanjad; E A Al-Sabban; R P Lifton; S W Scherer; F E Karet
Journal:  Nat Genet       Date:  2000-09       Impact factor: 38.330

7.  a4, a unique kidney-specific isoform of mouse vacuolar H+-ATPase subunit a.

Authors:  T Oka; Y Murata; M Namba; T Yoshimizu; T Toyomura; A Yamamoto; G H Sun-Wada; N Hamasaki; Y Wada; M Futai
Journal:  J Biol Chem       Date:  2001-08-09       Impact factor: 5.157

8.  Elevated expression of vacuolar proton pump genes and cellular PH in cisplatin resistance.

Authors:  T Murakami; I Shibuya; T Ise; Z S Chen; S Akiyama; M Nakagawa; H Izumi; T Nakamura; K Matsuo ; Y Yamada; K Kohno
Journal:  Int J Cancer       Date:  2001-09       Impact factor: 7.396

9.  Three subunit a isoforms of mouse vacuolar H(+)-ATPase. Preferential expression of the a3 isoform during osteoclast differentiation.

Authors:  T Toyomura; T Oka; C Yamaguchi; Y Wada; M Futai
Journal:  J Biol Chem       Date:  2000-03-24       Impact factor: 5.157

10.  Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis.

Authors:  A Frattini; P J Orchard; C Sobacchi; S Giliani; M Abinun; J P Mattsson; D J Keeling; A K Andersson; P Wallbrandt; L Zecca; L D Notarangelo; P Vezzoni; A Villa
Journal:  Nat Genet       Date:  2000-07       Impact factor: 38.330

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  89 in total

Review 1.  Regulation and isoform function of the V-ATPases.

Authors:  Masashi Toei; Regina Saum; Michael Forgac
Journal:  Biochemistry       Date:  2010-06-15       Impact factor: 3.162

2.  Inhibition of osteoclast bone resorption by disrupting vacuolar H+-ATPase a3-B2 subunit interaction.

Authors:  Norbert Kartner; Yeqi Yao; Keying Li; Gazelle J Crasto; Alessandro Datti; Morris F Manolson
Journal:  J Biol Chem       Date:  2010-09-13       Impact factor: 5.157

3.  Domain characterization and interaction of the yeast vacuolar ATPase subunit C with the peripheral stator stalk subunits E and G.

Authors:  Rebecca A Oot; Stephan Wilkens
Journal:  J Biol Chem       Date:  2010-06-07       Impact factor: 5.157

4.  Definition of membrane topology and identification of residues important for transport in subunit a of the vacuolar ATPase.

Authors:  Masashi Toei; Satoko Toei; Michael Forgac
Journal:  J Biol Chem       Date:  2011-08-08       Impact factor: 5.157

Review 5.  Dysregulated pH: a perfect storm for cancer progression.

Authors:  Bradley A Webb; Michael Chimenti; Matthew P Jacobson; Diane L Barber
Journal:  Nat Rev Cancer       Date:  2011-08-11       Impact factor: 60.716

Review 6.  Regulation of luminal acidification by the V-ATPase.

Authors:  Sylvie Breton; Dennis Brown
Journal:  Physiology (Bethesda)       Date:  2013-09

Review 7.  Proposed new lymphology combined with lymphatic physiology, innate immunology, and oncology.

Authors:  Toshio Ohhashi; Yoshiko Kawai
Journal:  J Physiol Sci       Date:  2014-11-07       Impact factor: 2.781

8.  Activity of plasma membrane V-ATPases is critical for the invasion of MDA-MB231 breast cancer cells.

Authors:  Kristina Cotter; Joseph Capecci; Souad Sennoune; Markus Huss; Martin Maier; Raul Martinez-Zaguilan; Michael Forgac
Journal:  J Biol Chem       Date:  2014-12-10       Impact factor: 5.157

9.  Models for the a subunits of the Thermus thermophilus V/A-ATPase and Saccharomyces cerevisiae V-ATPase enzymes by cryo-EM and evolutionary covariance.

Authors:  Daniel G Schep; Jianhua Zhao; John L Rubinstein
Journal:  Proc Natl Acad Sci U S A       Date:  2016-03-07       Impact factor: 11.205

Review 10.  Proton pump inhibitors as anti vacuolar-ATPases drugs: a novel anticancer strategy.

Authors:  Enrico P Spugnini; Gennaro Citro; Stefano Fais
Journal:  J Exp Clin Cancer Res       Date:  2010-05-08
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