Transformation of Cell-Derived Microparticles into Quantum-Dot-Labeled Nanovectors for Antitumor siRNA Delivery
Cell‐derived microparticles (MPs) have been recently recognized as critical intercellular information conveyors. However, further understanding of their biological behavior and potential application has been hampered by the limitations of current labeling techniques. Herein, a universal donor‐cell‐a...
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Published in: | Angewandte Chemie International Edition Vol. 54; no. 3; pp. 1036 - 1040 |
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Main Authors: | , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Weinheim
WILEY-VCH Verlag
12-01-2015
WILEY‐VCH Verlag Wiley Subscription Services, Inc |
Edition: | International ed. in English |
Subjects: | |
Online Access: | Get full text |
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Summary: | Cell‐derived microparticles (MPs) have been recently recognized as critical intercellular information conveyors. However, further understanding of their biological behavior and potential application has been hampered by the limitations of current labeling techniques. Herein, a universal donor‐cell‐assisted membrane biotinylation strategy was proposed for labeling MPs by skillfully utilizing the natural membrane phospholipid exchange of their donor cells. This innovative strategy conveniently led to specific, efficient, reproducible, and biocompatible quantum dot (QD) labeling of MPs, thereby reliably conferring valuable traceability on MPs. By further loading with small interference RNA, QD‐labeled MPs that had inherent cell‐targeting and biomolecule‐conveying ability were successfully employed for combined bioimaging and tumor‐targeted therapy. This study provides the first reliable and biofriendly strategy for transforming biogenic MPs into functionalized nanovectors.
Illuminating biogenic microparticles: Cell‐derived microparticles (MPs) are transformed to functionalized nanovectors by combining quantum dot (QD) labeling and efficient siRNA loading. This strategy not only reliably conferred excellent traceability and therapeutic potential on MPs, but also preserved their natural properties, thus facilitating the identification and further application of biogenic MPs. SA=streptavidin. |
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Bibliography: | istex:436658E51B77B4F089FBB358969C285B7CE00026 National Natural Science Foundation of China - No. 81300895; No. 81170977; No. 81371159 China Postdoctoral Science Foundation - No. 2013M540607 ark:/67375/WNG-G3R8CD4Q-G National Basic Research Program of China - No. 2011CB933600 This work was supported by the National Basic Research Program of China (973 Program, 2011CB933600), the National Natural Science Foundation of China (81300895, 81170977 and 81371159), the Doctoral Program Foundation of Higher Education of China (20130141120089 and 20130141130006), and the China Postdoctoral Science Foundation (2013M540607). ArticleID:ANIE201410223 Doctoral Program Foundation of Higher Education of China - No. 20130141120089; No. 20130141130006 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1433-7851 1521-3773 |
DOI: | 10.1002/anie.201410223 |