Literature DB >> 33634435

Innate Immunity Communicates Using the Language of Extracellular Microvesicles.

Mariusz Z Ratajczak1,2, Janina Ratajczak3.   

Abstract

The innate immunity system and extracellular microvesicles (ExMVs) both emerged early in the evolution of life, which is why its innate immunity cellular arm and its soluble-component arm learned, understood, and adapted to the "language" of ExMVs. This was most likely the first language of cell-cell communication during evolution, which existed before more specific intercellular crosstalk involving specific ligands and receptors emerged. ExMVs are involved in several processes in the body, including immune and coagulation responses, which are part of inflammation. In this review we will briefly highlight what is known about how ExMVs regulate the function of the cellular arm of innate immunity, including macrophages, monocytes, granulocytes, natural killer cells, and dendritic cells, and affect the soluble components of this system, which consists of the complement cascade (ComC) and soluble, circulating, pattern-recognition receptors (collectins, ficolins, and pentaxrins). These effects are direct, due to the fact that ExMVs affect the biological functions of innate immunity cells and may directly interact with soluble components of this system. Moreover, by activating coagulation proteases, ExMVs may also indirectly activate the ComC. In this review, we will use the term "extracellular microvesicles" (ExMVs) to refer to these small, spheroidal blebs of different sizes, which are surrounded by a membrane lipid layer. We will focus on the role of both ExMVs released during cell-surface membrane budding and smaller ExMVs, known as exosomes, which are derived from the budding of the endosomal membrane compartment. Finally, we will provide a brief update on the potential therapeutic applications of ExMVs, with a special emphasis on innate immunity.

Entities:  

Keywords:  Complement cascade; ExMVs; Exosomes; Horizontal transfer of RNA; Innate immunity; RNA

Mesh:

Year:  2021        PMID: 33634435      PMCID: PMC7906088          DOI: 10.1007/s12015-021-10138-6

Source DB:  PubMed          Journal:  Stem Cell Rev Rep        ISSN: 2629-3277            Impact factor:   5.739


  32 in total

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Journal:  Diabetes       Date:  2018-06-04       Impact factor: 9.461

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Journal:  Front Immunol       Date:  2020-09-02       Impact factor: 7.561

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Review 3.  Nanomaterial Exposure, Extracellular Vesicle Biogenesis and Adverse Cellular Outcomes: A Scoping Review.

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4.  Increased Circulating CD62E+ Endothelial Extracellular Vesicles Predict Severity and in- Hospital Mortality of COVID-19 Patients.

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5.  A systematic review and Meta-analysis of urinary extracellular vesicles proteome in diabetic nephropathy.

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