Abstract

A perifusion technique for microscopy with computerized detection of early changes in cell morphology during continuous perifusion was used to show that the geometry of cultured glioma cells (MG-251) changes rapidly when they are exposed to estramustine phosphate (EMP). When the cells were exposed to 20 or 40 mg l(-1) EMP, cell volume projected cell area (PCA) rapidly increased. When the Na+,K+-ATPase blocker ouabain (100 micromol l(-1)) was added to the EMP (40 mg l(-1)) perifusion, the acute EMP response was eradicated. When the PCA curve for ouabain alone was subtracted from the curve of combined ouabain and EMP perifusion, the resulting curve showed that ouabain completely blocked the EMP-induced increase in PCA. When the Na+, K+, Cl- co-transport inhibitors bumetanide (10 micromol l(-1)), or furosemide (100 micromol l(-1)), were added to EMP (40 mg l(-1)), the acute increase in PCA seen for EMP alone was also completely blocked. This study shows that inhibitors of ion transmembrane transport can modify EMP-induced cell volume increases. This may be of particular importance since the blockers have been found to interfere also with the cytotoxic function of EMP during cell culture. Thus, it is possible that cell volume changes could serve as a rapid technique for predicting the cytotoxic activity of antineoplastic drugs.

Highlights

  • We have investigated the effect of bumetanide and furosemide, inhibitors of Na+, K+, Cl- co-transport, and ouabain, an inhibitor of Na+, K+-ATPase, on the cytotoxic effect of estramustine phosphate (EMP)

  • We show that acute changes in cell size correlate strictly to the concentration of EMP in the perfusion systems

  • Neither was the projected cell area (PCA) slope calculated from medium change to the end of the perifusion significant: -0.13 ± 0.07% s-' (P < 0.20)

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Summary

Methods

The human malignant glioma cell line MG-251 was grown as monolayer culture in Eagle's minimal essential medium (MEM). The cells were incubated at 37°C in humidified atmosphere containing 5% carbon dioxide. Medium was changed three times a week. Cells were harvested by incubation with 0.2 ml of EDTA (5.0 mmol 1-') for 5 min followed by trypsin (0.1%). The cells were portioned into plastic tissue culture dishes containing basal medium and kept under controlled conditions (37°C and 5% carbon dioxide) before use. Estramustine phosphate [oestradiol-3-N-bis (chloroethyl) carbamate phosphate] was diluted in Eagle's MEM to appropriate concentrations and included in the incubation media

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