Potential Role of Sodium-Proton Exchangers in the Low Concentration Arsenic Trioxide-Increased Intracellular pH and Cell Proliferation

Aravena, C; Beltrán A.R.; Cornejo M.; Torres V.; Diaz E.S.; Guzman-Gutierrez, E; Pardo F.; Leiva A.; Sobrevia L.; Ramirez, M. A.

Abstract

Arsenic main inorganic compound is arsenic trioxide (ATO) presented in solution mainly as arsenite. ATO increases intracellular pH (pHi), cell proliferation and tumor growth. Sodium-proton exchangers (NHEs) modulate the pHi, with NHE1 playing significant roles. Whether ATO-increased cell proliferation results from altered NHEs expression and activity is unknown. We hypothesize that ATO increases cell proliferation by altering pHi due to increased NHEs-like transport activity. Madin-Darby canine kidney (MDCK) cells grown in 5 mmol/L D-glucose-containing DMEM were exposed to ATO (0.05, 0.5 or 5 μmol/L, 0-48 hours) in the absence or presence of 5-N,N-hexamethylene amiloride (HMA, 5-100 μmol/L, NHEs inhibitor), PD-98059 (30 μmol/L, MAPK1/2 inhibitor), Gö6976 (10 μmol/L, PKCα, βI and μ inhibitor), or Schering 28080 (10 μmol/L, H+/K+ATPase inhibitor) plus concanamycin (0.1 μmol/L, V type ATPases inhibitor). Incorporation of [3H]thymidine was used to estimate cell proliferation, and counting cells with a hemocytometer to determine the cell number. The pHi was measured by fluorometry in 2,7-bicarboxyethyl-5,6-carboxyfluorescein loaded cells. The Na+-dependent HMA-sensitive NHEs-like mediated proton transport kinetics, NHE1 protein abundance in the total, cytoplasm and plasma membrane protein fractions, and phosphorylated and total p42/44 mitogen-activated protein kinases (p42/44mapk) were also determined. Lowest ATO (0.05 μmol/L, ~0.01 ppm) used in this study increased cell proliferation, pHi, NHEs-like transport and plasma membrane NHE1 protein abundance, effects blocked by HMA, PD-98059 or Gö6976. Cell-buffering capacity did not change by ATO. The results show that a low ATO concentration increases MDCK cells proliferation by NHEs (probably NHE1)-like transport dependent-increased pHi requiring p42/44mapk and PKCα, βI and/or μ activity. This finding could be crucial in diseases where uncontrolled cell growth occurs, such as tumor growth, and in circumstances where ATO, likely arsenite, is available at the drinking-water at these levels. © 2012 Aravena et al.

Más información

Título según WOS: Potential Role of Sodium-Proton Exchangers in the Low Concentration Arsenic Trioxide-Increased Intracellular pH and Cell Proliferation
Título según SCOPUS: Potential Role of Sodium-Proton Exchangers in the Low Concentration Arsenic Trioxide-Increased Intracellular pH and Cell Proliferation
Título de la Revista: PLOS ONE
Volumen: 7
Número: 12
Editorial: PUBLIC LIBRARY SCIENCE
Fecha de publicación: 2012
Idioma: English
URL: http://www.scopus.com/inward/record.url?eid=2-s2.0-84870827215&partnerID=40&md5=bd05600702183dad1cffd3fbd81a522f
DOI:

10.1371/journal.pone.0051451

Notas: ISI, SCOPUS