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Biology
Akım Sitometri Kullanımı Ekstrasellüler Veziküller Analizi Teknikleri
Akım Sitometri Kullanımı Ekstrasellüler Veziküller Analizi Teknikleri
JoVE Journal
Biology
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JoVE Journal Biology
Techniques for the Analysis of Extracellular Vesicles Using Flow Cytometry

Akım Sitometri Kullanımı Ekstrasellüler Veziküller Analizi Teknikleri

Full Text
24,092 Views
09:39 min
March 17, 2015

DOI: 10.3791/52484-v

Heather Inglis1, Philip Norris1,2,3, Ali Danesh1,3

1Blood Systems Research Institute, 2Department of Medicine,University of California, San Francisco, 3Department of Laboratory Medicine,University of California, San Francisco

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Please note that some of the translations on this page are AI generated. Click here for the English version.

Overview

This article presents two methods for measuring extracellular vesicles (EVs) using flow cytometry (FCM). The methods include individual detection and a bead-based approach, each with specific protocols for isolating and analyzing EVs from blood samples.

Key Study Components

Area of Science

  • Neuroscience
  • Cell Biology
  • Flow Cytometry

Background

  • Extracellular vesicles (EVs) play a crucial role in intercellular communication.
  • Measuring EVs is important for understanding various biological processes.
  • Flow cytometry (FCM) is a widely used technique for EV analysis.
  • Different methods can yield varying results based on the approach used.

Purpose of Study

  • To isolate and analyze circulating extracellular vesicles in blood.
  • To compare individual detection and bead-based methods for EV measurement.
  • To provide protocols that researchers can follow for accurate EV analysis.

Methods Used

  • Isolation of platelet poor plasma (PPP) from blood samples.
  • Staining PPP with fluorochrome conjugated antibodies for individual detection.
  • Incubation of EVs with beads for the bead-based detection method.
  • Analysis of stained samples using flow cytometry.

Main Results

  • Both methods effectively measure circulating EVs.
  • Individual detection provides specific insights into EV characteristics.
  • The bead-based approach allows for multiplexing and enhanced sensitivity.
  • Flow cytometry analysis reveals the content and distribution of EVs.

Conclusions

  • Both methods are valid for measuring EVs, with unique advantages.
  • Researchers can choose the method based on their specific needs.
  • Understanding EV dynamics can contribute to advancements in biomedical research.

Frequently Asked Questions

What are extracellular vesicles?
Extracellular vesicles (EVs) are membrane-bound particles released by cells that play a role in cell communication and signaling.
Why is flow cytometry used for EV analysis?
Flow cytometry allows for the rapid and quantitative analysis of EVs based on their size and fluorescence characteristics.
What is the difference between individual detection and bead-based methods?
Individual detection focuses on analyzing single EVs, while bead-based methods use beads to capture and analyze multiple EVs simultaneously.
How is platelet poor plasma (PPP) obtained?
PPP is obtained by centrifuging blood samples to remove cells and platelets, leaving a clear plasma layer.
What role do fluorochrome conjugated antibodies play?
Fluorochrome conjugated antibodies bind to specific markers on EVs, allowing for their detection and analysis during flow cytometry.
Can these methods be used for clinical applications?
Yes, measuring EVs can have clinical implications, such as in disease diagnosis and monitoring therapeutic responses.

Pek çok farklı yöntem akış sitometrik (FCM) ile hücre dışı veziküller (EVS) ölçülmesi için vardır. Kullanmak için en uygun yöntemi belirlerken çeşitli yönleri dikkate alınmalıdır. Ölçüm EVs için iki protokoller bireysel algılama veya boncuk esaslı yaklaşım kullanılarak sunulmuştur.

Bu prosedürün genel amacı, kandaki hücre dışı vezikül dolaşımını iki farklı yöntemle izole etmek ve analiz etmektir. Bireysel hücre dışı vezikül tespit yöntemi için. Trombositten fakir plazma veya PPP ilk olarak bir kan örneğinden izole edilir.

PPP daha sonra ilgilenilen florokrom konjuge antikorlar ile boyanır. Boncuk bazlı tespit yöntemi için, hücre dışı veziküller boncuklarla inkübe edilir ve daha sonra boncuk bağlı veziküller ilgili florokrom konjuge antikorlarla boyanır. Sonuç olarak, dolaşımdaki hücre dışı vezikül içeriği, numunelerin akış sitometrisi ile analizi ile belirlenebilir.

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