Side-Directed Release of Differential Extracellular Vesicle-associated microRNA Profiles from Bronchial Epithelial Cells of Healthy and Asthmatic Subjects

• Published in: Biomedicines Vol. 10; no. 3; p. 622
• Main Authors: Schindler, Viktoria E. M., Alhamdan, Fahd, Preußer, Christian, Hintz, Lukas, Alashkar Alhamwe, Bilal, Nist, Andrea, Stiewe, Thorsten, Pogge von Strandmann, Elke, Potaczek, Daniel P., Thölken, Clemens, Garn, Holger
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 07.03.2022; MDPI
• Subjects: airway epithelium; Antibodies; Asthma; bronchial epithelial cells; Cell culture; Cell interactions; cellular compartmentalization; Cloning; Cytokines; Epithelial cells; extracellular vesicles; Flow cytometry; Gene expression; Lipids; MAP kinase; MicroRNAs; miRNA; miRNAs; Phenotypes; Proteins; Ribonucleic acid; RNA; Signal transduction; Software; Surface markers; TOR protein; United Kingdom > UK; United States > US; Germany; cellular compartmentalization; asthma; extracellular vesicles; bronchial epithelial cells; miRNAs; airway epithelium
• ISSN: 2227-9059; 2227-9059
• DOI: 10.3390/biomedicines10030622

Extracellular vesicles (EVs) are released by virtually all cells and may serve as intercellular communication structures by transmitting molecules such as proteins, lipids, and nucleic acids between cells. MicroRNAs (miRNAs) are an abundant class of vesicular RNA playing a pivotal role in regulating intracellular processes. In this work, we aimed to characterize vesicular miRNA profiles released in a side-directed manner by bronchial epithelial cells from healthy and asthmatic subjects using an air−liquid interface cell culture model. EVs were isolated from a culture medium collected from either the basolateral or apical cell side of the epithelial cell cultures and characterized by nano-flow cytometry (NanoFCM) and bead-based flow cytometry. EV-associated RNA profiles were assessed by small RNA sequencing and subsequent bioinformatic analyses. Furthermore, miRNA-associated functions and targets were predicted and miRNA network analyses were performed. EVs were released at higher numbers to the apical cell side of the epithelial cells and were considerably smaller in the apical compared to the basolateral compartment. EVs from both compartments showed a differential tetraspanins surface marker expression. Furthermore, 236 miRNAs were differentially expressed depending on the EV secretion side, regardless of the disease phenotype. On the apical cell side, 32 miRNAs were significantly altered in asthmatic versus healthy conditions, while on the basolateral cell side, 23 differentially expressed miRNAs could be detected. Downstream KEGG pathway analysis predicted mTOR and MAPK signaling pathways as potential downstream targets of apically secreted miRNAs. In contrast, miRNAs specifically detected at the basolateral side were associated with processes of T and B cell receptor signaling. The study proves a compartmentalized packaging of EVs by bronchial epithelial cells supposedly associated with site-specific functions of cargo miRNAs, which are considerably affected by disease conditions such as asthma.