Abstract
Constitutively released microvesicles (cMVs) are released as a part of normal cell physiology and this is summarised in Fig. 1 (1). However stimulated microvesicles (sMVs) are released as a result of a number of possible stress factors (2, 3). We found sMVs to be released in higher numbers than cMVs, typically ten-fold higher numbers, in the same time frame, and where the stress factor was a pharmacological agent, the microvesiculation was an attempt to release this chemical stress factor. Using a mass sensing technique, the sMVs were released over a 15 min period after stimulation. Using sizing beads on a flow cytometer and by transmission electron microscopy the cMVs were typically smaller (less than 300 nm in diameter) than sMVs (300-500 nm in diameter). However cMVs were found to carry more protein. By contrast, phosphatidylserine expression was greater on the larger sMVs, which also more effectively inhibited complement-mediated lysis.
Original language | English |
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Publication status | Published - 13 Sept 2012 |
Event | Microvesiculation and Disease, a Biochemical Society Focused Meeting: Microvesiculation and Disease - London Metropolitan University, London, United Kingdom Duration: 13 Sept 2012 → 14 Sept 2012 https://www.biochemistry.org/Events/tabid/379/View/programme/MeetingNo/SA133/Default.aspx |
Conference
Conference | Microvesiculation and Disease, a Biochemical Society Focused Meeting |
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Country/Territory | United Kingdom |
City | London |
Period | 13/09/12 → 14/09/12 |
Internet address |