Tumour cell proliferation is abolished by inhibitors of [formula omitted] and [formula omitted] exchange

Abstract

Cell membrane-associated ion transporters, Na + H + exchanger and Na +-dependent HCO 3 − Cl − antiport, were shown to be important in the regulation of acidic intracellular pH in different cell types. This study investigated the role of the ion exchangers and their inhibitors in the serum-induced proliferation of two murine tumour cell lines, P815 and L929. The presence of Na + H + exchanger [inhibited by amiloride and 5-( N-ethyl- N-isopropyl)amiloride (EIPA)] and Na +-dependent HCO 3 − Cl − antiport [inhibited by 4,4′diisothiocyanostilben-2,2-disulphonic acid (DIDS)] was shown on the tumour cell line tested. EIPA suppressed tumour cell proliferation more strongly than amiloride, and its effect was further increased after intracellular acidification by nigericin. DIDS slightly inhibited proliferation of L929 cell line and did not influence proliferation of P815 cells. However, in nigericin acidified cells DIDS had a dose dependent antiproliferative effect. Furthermore, DIDS significantly increased antiproliferative effects of amiloride and EIPA, suggesting the activity of Na +-dependent HCO 3 − Cl − antiport in tumour cell proliferation. These results demonstrate the importance of Na +-dependent HCO 3 − Cl − exchange in addition to Na + H + antiport, in tumour cell proliferation and indicate the possibility that ion exchange inhibitors could act as antitumour reagents.