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Cell membrane microfragments called microvesicles (MV) originating from different cells are circulating in the blood of healthy subjects and their elevated numbers are found in different diseases, including cancer. This study was designed to characterise MV present in plasma of gastric cancer patients. Since majority of MV in blood are platelets-derived (PMV), plasma samples deprived of PMV were used. In comparison to control, the number of MV in patients was significantly elevated in all stages, higher in more advanced disease. Patients' MV showed an increased membrane expression of CCR6 and HER-2/neu. The proportion of MV carrying some leucocyte determinants was low and similar in patients and control. Transmission electron microscopy showed their substantial heterogeneity in size and shape. The size determined by dynamic light scattering analysis confirmed this heterogeneity. The MV size distribution in patients was broader within the range of 10-800 nm, while in control MV showed 3-mode distribution within the range of 10-400 nm. Atomic force microscopy confirmed MV size heterogeneity with implication that larger objects represented aggregates of smaller microparticles. Patients' MV exhibited increased absolute values of zeta potential, indicating a higher surface charge. Tumour markers HER-2/neu, MAGE-1, c-MET and EMMPRIN were detected both in control and patients' samples with stronger expression in the latter. Significantly higher expression of MAGE-1 and HER-2/neu mRNA was observed in individual patients. All together, it suggests that at least some MV in plasma of gastric cancer patients are tumour-derived. However, their role in cancer requires further studies.

The zeta potentials of natural mica, bare and covered by positively charged latex particles of micrometer size range, were determined by the streaming potential method. Measurements were carried out using the parallel-plate channel formed by clamping together two mica sheets separated by a Teflon spacer. The dependence of streaming potential on surface coverage (ϑ) of adsorbed particles was determined for various ionic strengths and particle sizes. The coverage was determined directly by optical and electron microscope counting procedures. It was found that the negative streaming potential for bare mica E s was significantly increased by the presence of adsorbed particles. The dependence of the reduced streaming potential E s p /E s (where E s p is the zeta potential in the presence of particles) on ϑ exhibited an universal behavior being independent of particle size and ionic strength. These experimental data were interpreted in terms of a theoretical model postulating that the streaming potential change was due to flow damping over the interface and by charge transport from the double-layer surrounding adsorbed particles. In contrast with previous approaches no assumption of the slip (shear) plane shift upon particle adsorption was made. By exploiting the experimental results it was suggested that colloid and bioparticle adsorption kinetics can be studied in situ using the streaming potential method.

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