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Ligand-competent fractalkine receptor is expressed on exosomes

Expression of chemokine receptor CX3CR1 is reportedly restricted to several cell types including natural killer cells, cytotoxic T cells, monocytes, and macrophages. However, its expression and function on exosomes, which are nanosized extracellular vesicles known to act as mediators of intercellula...

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Autores principales: Park, Eun Jeong, Myint, Phyoe Kyawe, Appiah, Michael G., Worawattananutai, Patsorn, Inprasit, Janjira, Prajuabjinda, Onmanee, Soe, Zay Yar, Gaowa, Arong, Kawamoto, Eiji, Shimaoka, Motomu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7859287/
https://www.ncbi.nlm.nih.gov/pubmed/33553692
http://dx.doi.org/10.1016/j.bbrep.2021.100932
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author Park, Eun Jeong
Myint, Phyoe Kyawe
Appiah, Michael G.
Worawattananutai, Patsorn
Inprasit, Janjira
Prajuabjinda, Onmanee
Soe, Zay Yar
Gaowa, Arong
Kawamoto, Eiji
Shimaoka, Motomu
author_facet Park, Eun Jeong
Myint, Phyoe Kyawe
Appiah, Michael G.
Worawattananutai, Patsorn
Inprasit, Janjira
Prajuabjinda, Onmanee
Soe, Zay Yar
Gaowa, Arong
Kawamoto, Eiji
Shimaoka, Motomu
author_sort Park, Eun Jeong
collection PubMed
description Expression of chemokine receptor CX3CR1 is reportedly restricted to several cell types including natural killer cells, cytotoxic T cells, monocytes, and macrophages. However, its expression and function on exosomes, which are nanosized extracellular vesicles known to act as mediators of intercellular communications, remain unclear. Here, we investigated CX3CR1 expression on exosomes isolated from various cell types. Although we found that all the exosomes tested in our study highly expressed CX3CR1, this chemokine receptor was expressed only inside, but barely on, their source cells. Moreover, exosomal CX3CR1 was capable of binding soluble CX3CL1. Therefore, our study suggests that CX3CR1 is a novel and ligand-competent exosome receptor.
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spelling pubmed-78592872021-02-05 Ligand-competent fractalkine receptor is expressed on exosomes Park, Eun Jeong Myint, Phyoe Kyawe Appiah, Michael G. Worawattananutai, Patsorn Inprasit, Janjira Prajuabjinda, Onmanee Soe, Zay Yar Gaowa, Arong Kawamoto, Eiji Shimaoka, Motomu Biochem Biophys Rep Research Article Expression of chemokine receptor CX3CR1 is reportedly restricted to several cell types including natural killer cells, cytotoxic T cells, monocytes, and macrophages. However, its expression and function on exosomes, which are nanosized extracellular vesicles known to act as mediators of intercellular communications, remain unclear. Here, we investigated CX3CR1 expression on exosomes isolated from various cell types. Although we found that all the exosomes tested in our study highly expressed CX3CR1, this chemokine receptor was expressed only inside, but barely on, their source cells. Moreover, exosomal CX3CR1 was capable of binding soluble CX3CL1. Therefore, our study suggests that CX3CR1 is a novel and ligand-competent exosome receptor. Elsevier 2021-02-02 /pmc/articles/PMC7859287/ /pubmed/33553692 http://dx.doi.org/10.1016/j.bbrep.2021.100932 Text en © 2021 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Article
Park, Eun Jeong
Myint, Phyoe Kyawe
Appiah, Michael G.
Worawattananutai, Patsorn
Inprasit, Janjira
Prajuabjinda, Onmanee
Soe, Zay Yar
Gaowa, Arong
Kawamoto, Eiji
Shimaoka, Motomu
Ligand-competent fractalkine receptor is expressed on exosomes
title Ligand-competent fractalkine receptor is expressed on exosomes
title_full Ligand-competent fractalkine receptor is expressed on exosomes
title_fullStr Ligand-competent fractalkine receptor is expressed on exosomes
title_full_unstemmed Ligand-competent fractalkine receptor is expressed on exosomes
title_short Ligand-competent fractalkine receptor is expressed on exosomes
title_sort ligand-competent fractalkine receptor is expressed on exosomes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7859287/
https://www.ncbi.nlm.nih.gov/pubmed/33553692
http://dx.doi.org/10.1016/j.bbrep.2021.100932
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