Literature DB >> 28254382

A direct-imaging cryo-EM study of shedding extracellular vesicles from leukemic monocytes.

Na'ama Koifman1, Idan Biran1, Anat Aharon2, Benjamin Brenner2, Yeshayahu Talmon3.   

Abstract

The human leukemia monocytic cell line (THP-1) is known to shed extracellular vesicles (EVs) under various stimulations. We studied the effects of two types of common stimulation types, lipopolysaccharide (LPS) and starvation conditions by high resolution cryogenic electron microscopy, namely, cryo-SEM and cryo-TEM. Cryo-SEM data of cells undergoing EV blebbing and shedding is presented here for the first time. The high-resolution images show good agreement with models describing the membrane processes of shedding. Cells that underwent a 48-h starvation treatment exhibited differing morphological features, including shrunken nucleus and elongated membrane protrusions. LPS treated cells, however, showed extensive blebbing originating from the cell membrane, in good agreement with the sizes of EVs imaged by cryo-TEM. EVs isolated from both types of stimulations were measured by nanoparticle tracking analysis (NanoSight), by which LPS-EVs samples exhibited higher concentration and smaller mean diameter, as compared to starvation-EVs. Our results suggest a difference in the effects of the two stimulation types on the shedding process and possibly on the type of EVs shed. Our unique methodologies provide an important and innovative outlook of the shedding process and on its products, paving the way to further discoveries in this developing field of research, in which much is still unknown.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Blebbing; Cell stimulation; Cryo-EM; Endotoxins; Microparticles; NTA

Mesh:

Substances:

Year:  2017        PMID: 28254382     DOI: 10.1016/j.jsb.2017.02.004

Source DB:  PubMed          Journal:  J Struct Biol        ISSN: 1047-8477            Impact factor:   2.867


  16 in total

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2.  Direct comparison of optical and electron microscopy methods for structural characterization of extracellular vesicles.

Authors:  Jade M Noble; LaDeidra Monét Roberts; Netta Vidavsky; Aaron E Chiou; Claudia Fischbach; Matthew J Paszek; Lara A Estroff; Lena F Kourkoutis
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Authors:  Charlotte Volgers; Gert E Grauls; Pauline H M Hellebrand; Paul H M Savelkoul; Frank R M Stassen
Journal:  Inflammopharmacology       Date:  2017-05-20       Impact factor: 4.473

Review 7.  Technologies and Standardization in Research on Extracellular Vesicles.

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Journal:  Trends Biotechnol       Date:  2020-06-18       Impact factor: 19.536

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9.  Extracellular vesicles provide a capsid-free vector for oncolytic adenoviral DNA delivery.

Authors:  Heikki Saari; Tiia Turunen; Andres Lõhmus; Mikko Turunen; Matti Jalasvuori; Sarah J Butcher; Seppo Ylä-Herttuala; Tapani Viitala; Vincenzo Cerullo; Pia R M Siljander; Marjo Yliperttula
Journal:  J Extracell Vesicles       Date:  2020-04-17

Review 10.  Message in a Bottle: Upgrading Cardiac Repair into Rejuvenation.

Authors:  Carolina Balbi; Ambra Costa; Lucio Barile; Sveva Bollini
Journal:  Cells       Date:  2020-03-15       Impact factor: 6.600

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