Utilizing Extracellular Vesicles for Eliminating 'Unwanted Molecules': Harnessing Nature's Structures in Modern Therapeutic Strategies.
Monika KisielewskaKatarzyna RakoczyIzabela SkowronJulia GórczyńskaJulia KacerAgata BocheńskaAnna ChoromanskaPublished in: Molecules (Basel, Switzerland) (2024)
Extracellular vesicles (EVs) are small phospholipid bilayer-bond structures released by diverse cell types into the extracellular environment, maintaining homeostasis of the cell by balancing cellular stress. This article provides a comprehensive overview of extracellular vesicles, their heterogeneity, and diversified roles in cellular processes, emphasizing their importance in the elimination of unwanted molecules. They play a role in regulating oxidative stress, particularly by discarding oxidized toxic molecules. Furthermore, endoplasmic reticulum stress induces the release of EVs, contributing to distinct results, including autophagy or ER stress transmission to following cells. ER stress-induced autophagy is a part of unfolded protein response (UPR) and protects cells from ER stress-related apoptosis. Mitochondrial-derived vesicles (MDVs) also play a role in maintaining homeostasis, as they carry damaged mitochondrial components, thereby preventing inflammation. Moreover, EVs partake in regulating aging-related processes, and therefore they can potentially play a crucial role in anti-aging therapies, including the treatment of age-related diseases such as Alzheimer's disease or cardiovascular conditions. Overall, the purpose of this article is to provide a better understanding of EVs as significant mediators in both physiological and pathological processes, and to shed light on their potential for therapeutic interventions targeting EV-mediated pathways in various pathological conditions, with an emphasis on age-related diseases.
Keyphrases
- endoplasmic reticulum stress
- induced apoptosis
- oxidative stress
- stress induced
- single cell
- ischemia reperfusion injury
- cell death
- dna damage
- diabetic rats
- cell cycle arrest
- signaling pathway
- cell therapy
- stem cells
- bone marrow
- big data
- cancer therapy
- combination therapy
- cognitive decline
- heat stress
- amino acid
- mass spectrometry
- protein protein