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dc.contributor.authorStratton, Dan
dc.contributor.authorInal, Jameel
dc.date.accessioned2018-07-31T12:50:47Z
dc.date.available2018-07-31T12:50:47Z
dc.date.issued2012-09-13
dc.identifier.citationStratton , D & Inal , J 2012 , ' Characterisation of microvesicles released from cells constitutively and upon stimulation ' , Microvesiculation and Disease, a Biochemical Society Focused Meeting , London , United Kingdom , 13/09/12 - 14/09/12 .
dc.identifier.citationconference
dc.identifier.urihttp://hdl.handle.net/2299/20308
dc.description.abstractConstitutively 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.en
dc.format.extent104776
dc.language.isoeng
dc.titleCharacterisation of microvesicles released from cells constitutively and upon stimulationen
dc.contributor.institutionSchool of Life and Medical Sciences
dc.contributor.institutionDepartment of Biological and Environmental Sciences
dc.contributor.institutionBiosciences Research Group
dc.description.statusPeer reviewed
rioxxterms.typeOther
herts.preservation.rarelyaccessedtrue


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