کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1931633 1050560 2010 5 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Red cell PMVs, plasma membrane-derived vesicles calling out for standards
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شیمی
پیش نمایش صفحه اول مقاله
Red cell PMVs, plasma membrane-derived vesicles calling out for standards
چکیده انگلیسی

Plasma membrane-derived vesicles (PMVs) or microparticles are vesicles (0.1–1 μm in diameter) released from the plasma membrane of all blood cell types under a variety of biochemical and pathological conditions. PMVs contain cytoskeletal elements and some surface markers from the parent cell but lack a nucleus and are unable to synthesise macromolecules. They are also defined on the basis that in most cases PMVs express varying amounts of the cytosolic leaflet lipid phosphatidylserine, which is externalised during activation on their surface. This marks the PMV as a biologically distinct entity from that of its parent cell, despite containing surface markers from the original cell, and also explains its role in events such as phagocytosis and thrombosis. There is currently a large amount of variation between investigators with regard to the pre-analytical steps employed in isolating red cell PMVs or RPMVs (which are slightly smaller than most PMVs), with key differences being centrifugation and sample storage conditions, which often leads to result variability. Unfortunately, standardization of preparation and detection methods has not yet been achieved. This review highlights and critically discusses the variables contributing to differences in results obtained by investigators, bringing to light numerous studies of which RPMVs have been analysed but have not yet been the subject of a review.

Research highlights
► Red cell Plasma Membrane-derived Vesicles (RPMVs) are the most numerous PMVs in plasma.
► RPMVs are implicated in a number of pathological states.
► RPMV isolation and detection is not standardised.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biochemical and Biophysical Research Communications - Volume 399, Issue 4, 3 September 2010, Pages 465–469
نویسندگان
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