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Microvesicles were isolated from the conditioned media of 3 cell lines (MDA‐MB‐231, AsPC‐1 and A375) by ultracentrifugation at a range of relative centrifugal forces, and the tissue factor (TF) protein and activity, microvesicle number, size distribution and relative density compared. Also, by expressing TF‐tGFP in cells and isolating the microvesicles, the relative density of TF‐containing microvesicles was established. Nanoparticle tracking analysis (NTA) indicated that the larger‐diameter microvesicles (>200 nm) were primarily sedimented at 100,000 g  and possessed TF‐dependent thrombin and factor Xa generation potential, while in the absence of factor VII, all microvesicles possessed some thrombin generation capacity. Immuno‐precipitation of TF‐containing microvesicles followed by NTA also indicated the range of these microvesicles to be 200–400 nm. Analysis of the microvesicles by gradient density centrifugation showed that lower‐density (<1.1 g/ml) microvesicles were mainly present in the samples recovered at 100,000 g  and were associated with TF antigen and activity. Analysis of these fractions by NTA confirmed that these fractions were principally composed of the larger‐diameter microvesicles. Similar analysis of microvesicles from healthy or patient plasma supported those obtained from conditioned media indicating that TF activity was mainly associated with lower‐density microvesicles. Furthermore, centrifugation of healthy plasma, supplemented with TF‐tGFP‐containing microvesicles, resulted in 67% retrieval of the fluorescent microvesicles at 100,000 g , but only 26% could be recovered at 20,000 g . Pre‐centrifugation of conditioned media or plasma at 10,000 g  improved the speed and yield of recovered TF‐containing microvesicles by subsequent centrifugation at either 20,000 g  or 100,000 g . In conclusion, TF appears to be associated with low‐density (1.03–1.08 g/ml), larger‐diameter (200–350 nm) microvesicles.

Characterization of physical properties of tissue factor–containing microvesicles and a comparison of ultracentrifuge‐based recovery procedures