Purinergic enzymes on extracellular vesicles: immune modulation on the go

Front Immunol. 2024 Feb 15:15:1362996. doi: 10.3389/fimmu.2024.1362996. eCollection 2024.

Abstract

An increase in the extracellular concentration of ATP as a consequence of cellular stress or cell death results in the activation of immune cells. To prevent inflammation, extracellular ATP is rapidly metabolized to adenosine, which deploys an anti-inflammatory signaling cascade upon binding to P1 receptors on immune cells. The ectonucleotidases necessary for the degradation of ATP and generation of adenosine are present on the cell membrane of many immune cells, and their expression is tightly regulated under conditions of inflammation. The discovery that extracellular vesicles (EVs) carry purinergic enzyme activity has brought forward the concept of EVs as a new player in immune regulation. Adenosine-generating EVs derived from cancer cells suppress the anti-tumor response, while EVs derived from immune or mesenchymal stem cells contribute to the restoration of homeostasis after infection. Here we will review the existing knowledge on EVs containing purinergic enzymes and molecules, and discuss the relevance of these EVs in immune modulation and their potential for therapy.

Keywords: CD73; adenosine; extracellular vesicles; immune regulation; purinergic signaling; tumor microenvironment.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Adenosine* / metabolism
  • Extracellular Vesicles* / metabolism
  • Humans
  • Immunity
  • Inflammation

Substances

  • Adenosine
  • Adenosine Triphosphate

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. Work on the purinergic system in our research groups is supported by the German Research Council SFB 1328 (Project-ID: 335447717 to ET and NG, subproject A14) and FOR 2879 ImmunoStroke (Project-ID: 405358801 to ET, subproject C1). We acknowledge financial support from the Open Access Publication Fund of UKE - Universitätsklinikum Hamburg-Eppendorf and DFG – German Research Foundation