| Literature DB >> 33553692 |
Eun Jeong Park1, Phyoe Kyawe Myint1, Michael G Appiah1, Patsorn Worawattananutai1, Janjira Inprasit1, Onmanee Prajuabjinda1, Zay Yar Soe1, Arong Gaowa1, Eiji Kawamoto1,2, Motomu Shimaoka1.
Abstract
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.Entities:
Keywords: CX3CR1; Chemokine; Chemokine receptor; Exosome; Fractalkine
Year: 2021 PMID: 33553692 PMCID: PMC7859287 DOI: 10.1016/j.bbrep.2021.100932
Source DB: PubMed Journal: Biochem Biophys Rep ISSN: 2405-5808