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Review
. 2020 May 27:2020:2319616.
doi: 10.1155/2020/2319616. eCollection 2020.

Exosomes: Potential Therapies for Disease via Regulating TLRs

Affiliations
Review

Exosomes: Potential Therapies for Disease via Regulating TLRs

Hong-Yan Guo et al. Mediators Inflamm. .

Abstract

Exosomes are small membrane vesicles that retain various substances such as proteins, nucleic acids, and small RNAs. Exosomes play crucial roles in many physiological and pathological processes, including innate immunity. Innate immunity is an important process that protects the organism through activating pattern recognition receptors (PRRs), which then can induce inflammatory factors to resist pathogen invasion. Toll-like receptor (TLR) is one member of PRRs and is important in pathogen clearance and nervous disease development. Although exosomes and TLRs are two independent materials, abundant evidences imply exosomes can regulate innate immunity through integrating with TLRs. Herein, we review the most recent data regarding exosome regulation of TLR pathways. Specifically, exosome-containing materials can regulate TLR pathways through the interaction with TLRs. This is a new strategy regulating immunity to resist pathogens and therapy diseases, which provide a potential method to cure diseases.

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Conflict of interest statement

The authors declare that there is no conflict of interest regarding this publication.

Figures

Figure 1
Figure 1
The formation and transportation of exosome. The formation of a mature exosome is closely related to two processes. First, the limiting membrane is invaginated to form multivescular bodies (MVB). Second, a part of MVBs called exocytic MVBs bud off into the lumen of the late endosome to form the second membrane and then secrete into the extracellular space along with their cargo, while another part of MVBs evolve into lysosomes for degradation called degradative MVBs. Then, exosomes are translated by body fluid and the three ways for receipt cell to take up exosomes are ➀ endocytosis, ➁ lipid raft-mediated internalization, and ➂ by combining with the target cell membrane directly.

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