Literature DB >> 22767229

Prion-infected cells regulate the release of exosomes with distinct ultrastructural features.

Bradley M Coleman1, Eric Hanssen, Victoria A Lawson, Andrew F Hill.   

Abstract

Exosomes are small membrane-bound vesicles released from cells and found in vivo in most biological fluids. Functions reported for exosomes include cell-cell communication, roles in modulating immune responses, and roles in the transfer of pathogens such as prions. Here we investigated the molecular characteristics of the structure of exosomes that harbor prion infectivity to determine the native structure of exosomes and whether infected exosomes have a distinct structure. Cryo-electron tomography revealed the previously unidentified ultrastructural detail of exosomes with high resolution. Exosomes were found to be naturally spherical in shape and to have a diverse population that varies in size and internal structure, such as differences in the number of membrane structures. Exosomes isolated from prion-infected cells contained a significantly different population of exosomes with distinct structural features compared to control vesicles from mock-infected cells. Exosomes are highly structured vesicles that can modify their structure on altering their protein cargo. This finding provides further insight into the role that the exosomal protein cargo plays on influencing the structure of the vesicles as well as highlighting the diversity of exosomes and their relationship to biological processes.

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Year:  2012        PMID: 22767229     DOI: 10.1096/fj.11-202077

Source DB:  PubMed          Journal:  FASEB J        ISSN: 0892-6638            Impact factor:   5.191


  61 in total

Review 1.  Exosomes function in cell-cell communication during brain circuit development.

Authors:  Pranav Sharma; Lucio Schiapparelli; Hollis T Cline
Journal:  Curr Opin Neurobiol       Date:  2013-08-30       Impact factor: 6.627

2.  First demonstration of transmissible spongiform encephalopathy-associated prion protein (PrPTSE) in extracellular vesicles from plasma of mice infected with mouse-adapted variant Creutzfeldt-Jakob disease by in vitro amplification.

Authors:  Paula Saá; Oksana Yakovleva; Jorge de Castro; Irina Vasilyeva; Silvia H De Paoli; Jan Simak; Larisa Cervenakova
Journal:  J Biol Chem       Date:  2014-08-25       Impact factor: 5.157

3.  Breast Cancer-Specific miR Signature Unique to Extracellular Vesicles Includes "microRNA-like" tRNA Fragments.

Authors:  Nicole Guzman; Kitty Agarwal; Dilip Asthagiri; Lianbo Yu; Motoyasu Saji; Matthew D Ringel; Michael E Paulaitis
Journal:  Mol Cancer Res       Date:  2015-02-26       Impact factor: 5.852

4.  Microencapsulation technology by nature: Cell derived extracellular vesicles with therapeutic potential.

Authors:  A Kittel; A Falus; E Buzás
Journal:  Eur J Microbiol Immunol (Bp)       Date:  2013-06-05

5.  Efficient inhibition of infectious prions multiplication and release by targeting the exosomal pathway.

Authors:  Didier Vilette; Karine Laulagnier; Alvina Huor; Sandrine Alais; Sabrina Simoes; Romao Maryse; Monique Provansal; Sylvain Lehmann; Olivier Andreoletti; Laurent Schaeffer; Graça Raposo; Pascal Leblanc
Journal:  Cell Mol Life Sci       Date:  2015-06-06       Impact factor: 9.261

6.  Extracellular vesicles as modulators of cell-to-cell communication in the healthy and diseased brain.

Authors:  D M Pegtel; L Peferoen; S Amor
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2014-09-26       Impact factor: 6.237

7.  Nanoscale lateral displacement arrays for the separation of exosomes and colloids down to 20 nm.

Authors:  Benjamin H Wunsch; Joshua T Smith; Stacey M Gifford; Chao Wang; Markus Brink; Robert L Bruce; Robert H Austin; Gustavo Stolovitzky; Yann Astier
Journal:  Nat Nanotechnol       Date:  2016-08-01       Impact factor: 39.213

8.  Prognostic serum miRNA biomarkers associated with Alzheimer's disease shows concordance with neuropsychological and neuroimaging assessment.

Authors:  L Cheng; J D Doecke; R A Sharples; V L Villemagne; C J Fowler; A Rembach; R N Martins; C C Rowe; S L Macaulay; C L Masters; A F Hill
Journal:  Mol Psychiatry       Date:  2014-10-28       Impact factor: 15.992

9.  Pathogenic mutations within the hydrophobic domain of the prion protein lead to the formation of protease-sensitive prion species with increased lethality.

Authors:  Bradley M Coleman; Christopher F Harrison; Belinda Guo; Colin L Masters; Kevin J Barnham; Victoria A Lawson; Andrew F Hill
Journal:  J Virol       Date:  2013-12-18       Impact factor: 5.103

10.  Analysis of exosome release as a cellular response to MAPK pathway inhibition.

Authors:  K Agarwal; M Saji; S M Lazaroff; A F Palmer; M D Ringel; M E Paulaitis
Journal:  Langmuir       Date:  2015-05-05       Impact factor: 3.882

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