“…Due to the surrounding lipid membrane, EVs prevent degradation of the transported lipid mediators (e.g., eicosanoids), proteins (cytokines, chemokines, growth factors), genetic material (mRNA, long non-coding RNAs, short non-coding RNAs/miRs, nuclear and mitochondrial DNA) and organelles (e.g., mitochondria) by enzymes. EVs in the bronchoalveolar fluid (BALF) are mainly lung-specific exosomes, suggesting that exosomes predominantly serve for local signaling [ 52 ] with most cross talk taking place between alveolar epithelial cells and alveolar macrophages. Lung cells communicate intensely via EVs, which are released by respiratory cells at the apical and at the basal site, by alveolar macrophages, by other immune cells in the lungs and by fibroblasts [ 53 ].…”