» Articles » PMID: 39697631

Hitting the Target: Cell Signaling Pathways Modulation by Extracellular Vesicles

Overview
Authors
Affiliations
Soon will be listed here.
Abstract

Extracellular vesicles (EVs) are lipid bilayer-enclosed nanoparticles released outside the cell. EVs have drawn attention not only for their role in cell waste disposal, but also as additional tools for cell-to-cell communication. Their complex contents include not only lipids, but also proteins, nucleic acids (RNA, DNA), and metabolites. A large part of these molecules are involved in mediating or influencing signal transduction in target cells. In multicellular organisms, EVs have been suggested to modulate signals in cells localized either in the neighboring tissue or in distant regions of the body by interacting with the cell surface or by entering the cells via endocytosis or membrane fusion. Most of the EV-modulated cell signaling pathways have drawn considerable attention because they affect morphogenetic signaling pathways, as well as pathways activated by cytokines and growth factors. Therefore, they are implicated in relevant biological processes, such as embryonic development, cancer initiation and spreading, tissue differentiation and repair, and immune response. Furthermore, it has recently emerged that multicellular organisms interact with and receive signals through EVs released by their microbiota as well as by edible plants. This review reports studies investigating EV-mediated signaling in target mammalian cells, with a focus on key pathways for organism development, organ homeostasis, cell differentiation and immune response.

Citing Articles

Extracellular Vesicles as Mediators of Endothelial Dysfunction in Cardiovascular Diseases.

Jimenez-Trinidad F, Calvo-Gomez S, Sabate M, Brugaletta S, Campuzano V, Egea G Int J Mol Sci. 2025; 26(3).

PMID: 39940780 PMC: 11816526. DOI: 10.3390/ijms26031008.

References
1.
Skog J, Wurdinger T, van Rijn S, Meijer D, Gainche L, Sena-Esteves M . Glioblastoma microvesicles transport RNA and proteins that promote tumour growth and provide diagnostic biomarkers. Nat Cell Biol. 2008; 10(12):1470-6. PMC: 3423894. DOI: 10.1038/ncb1800. View

2.
Zhang Y, Meng J, Zhang L, Ramkrishnan S, Roy S . Extracellular Vesicles with Exosome-like Features Transfer TLRs between Dendritic Cells. Immunohorizons. 2019; 3(6):186-193. PMC: 8011940. DOI: 10.4049/immunohorizons.1900016. View

3.
Liu Y, Xiang X, Zhuang X, Zhang S, Liu C, Cheng Z . Contribution of MyD88 to the tumor exosome-mediated induction of myeloid derived suppressor cells. Am J Pathol. 2010; 176(5):2490-9. PMC: 2861113. DOI: 10.2353/ajpath.2010.090777. View

4.
Pucci M, Raimondo S, Urzi O, Moschetti M, Di Bella M, Conigliaro A . Tumor-Derived Small Extracellular Vesicles Induce Pro-Inflammatory Cytokine Expression and PD-L1 Regulation in M0 Macrophages via IL-6/STAT3 and TLR4 Signaling Pathways. Int J Mol Sci. 2021; 22(22). PMC: 8621495. DOI: 10.3390/ijms222212118. View

5.
Gu J, Qian H, Shen L, Zhang X, Zhu W, Huang L . Gastric cancer exosomes trigger differentiation of umbilical cord derived mesenchymal stem cells to carcinoma-associated fibroblasts through TGF-β/Smad pathway. PLoS One. 2013; 7(12):e52465. PMC: 3527492. DOI: 10.1371/journal.pone.0052465. View