Literature DB >> 23731456

Cellular communication via nanoparticle-transporting biovesicles.

Silvia Ferrati1, Kellie I McConnell1, Aaron C Mack1, Natalie Sirisaengtaksin2, Rodrigo Diaz1, Andrew J Bean2,3, Mauro Ferrari1, Rita E Serda1.   

Abstract

AIMS: Endothelial cells are dynamic cells tasked with selective transport of cargo from blood vessels to tissues. Here we demonstrate the potential for nanoparticle transport across endothelial cells in membrane-bound vesicles. MATERIALS &
METHODS: Cell-free endothelial-derived biovesicles were characterized for cellular and nanoparticle content by electron microscopy. Confocal microscopy was used to evaluate biovesicles for organelle-specific proteins, and to monitor biovesicle engulfment by naive cells.
RESULTS: Nanoparticle-laden biovesicles containing low-density polyethyleneimine nanoparticles appear to be predominately of endosomal origin, combining features of multivesicular bodies, lysosomes and autophagosomes. Conversely, high-density polyethyleneimine nanoparticles stimulate the formation of biovesicles associated with cellular apoptotic breakdown. Secreted LAMP-1-positive biovesicles are internalized by recipient cells, either of the same origin or of novel phenotype.
CONCLUSION: Cellular biovesicles, rich in cellular signals, present an important mode of cell-to-cell communication either locally or through broadcasting of biological messages.

Entities:  

Keywords:  biovesicle; endothelia; exocytosis; iron oxide; microvesicle; nanoparticle

Mesh:

Year:  2013        PMID: 23731456      PMCID: PMC3947494          DOI: 10.2217/nnm.13.57

Source DB:  PubMed          Journal:  Nanomedicine (Lond)        ISSN: 1743-5889            Impact factor:   5.307


  28 in total

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