کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
33043 44954 2016 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Development of a magnetic bead-based method for the collection of circulating extracellular vesicles
ترجمه فارسی عنوان
توسعه یک روش مبتنی بر مغناطیسی برای جمع آوری غشاء خارج سلول گردش
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی بیو مهندسی (مهندسی زیستی)
چکیده انگلیسی


• Apoptotic bodies captured by ANX-beads contained both DNA and amplifiable RNA.
• Plasma EVs can be captured with ANX-beads.
• Tumor-derived EVs could be found in body fluids.

Cells release different types of extracellular vesicles (EVs). These EVs contain biomolecules, including proteins and nucleic acids, from their parent cells, which can be useful for diagnostic applications. The aim of this study was to develop a convenient procedure to collect circulating EVs with detectable mRNA or other biomolecules. Magnetic beads coated with annexin A5 (ANX-beads), which bound to phosphatidylserine moieties on the surfaces of most EVs, were tested for their ability to capture induced apoptotic bodies in vitro and other phosphatidylserine-presenting vesicles in body fluids. Our results show that up to 60% of induced apoptotic bodies could be captured by the ANX-beads. The vesicles captured from cultured media or plasma contained amplifiable RNA. Suitable blood samples for EV collection included EDTA-plasma and serum but not heparin-plasma. In addition, EVs in plasma were labile to freeze-and-thaw cycles. In rodents xenografted with human cancer cells, tumor-derived mRNA could be detected in EVs captured from serum samples. Active proteins could be detected in EVs captured from ascites but not from plasma. In conclusion, we have developed a magnetic bead-based procedure for the collection of EVs from body fluids and proved that captured EVs contain biomolecules from their parent cells, and therefore have great potential for disease diagnosis.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: New Biotechnology - Volume 33, Issue 1, 25 January 2016, Pages 116–122
نویسندگان
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