MicroRNA-Enriched Exosomes from Different Sources of Mesenchymal Stem Cells Can Differentially Modulate Functions of Immune Cells and Neurogenesis

• Published in: Biomedicines Vol. 10; no. 1; p. 69
• Main Authors: Soni, Naina, Gupta, Suchi, Rawat, Surender, Krishnakumar, Vishnu, Mohanty, Sujata, Banerjee, Arup
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 30.12.2021; MDPI
• Subjects: Angiogenesis; Biological activity; Body fat; Bone marrow; Consent; Ethics; Exosomes; Experiments; Leukocytes (neutrophilic); Mesenchymal stem cells; MicroRNAs; miRNA; Neurogenesis; neutrophils; PBMC; Peripheral blood mononuclear cells; Proteins; Stem cells; St Louis Missouri; United States > US; India; neurogenesis; miRNA; PBMC; neutrophils; exosomes; mesenchymal stem cells
• ISSN: 2227-9059; 2227-9059
• DOI: 10.3390/biomedicines10010069

Adult Mesenchymal stem cells-derived exosomes carry several biologically active molecules that play prominent roles in controlling disease manifestations. The content of these exosomes, their functions, and effect on the immune cells may differ depending on their tissue sources. Therefore, in this study, we purified the exosomes from three different sources and, using the RNA-Seq approach, highly abundant microRNAs were identified and compared between exosomes and parental cells. The effects of exosomes on different immune cells were studied in vitro by incubating exosomes with PBMC and neutrophils and assessing their functions. The expression levels of several miRNAs varied within the different MSCs and exosomes. Additionally, the expression profile of most of the miRNAs was not similar to that of their respective sources. Exosomes isolated from different sources had different abilities to induce the process of neurogenesis and angiogenesis. Moreover, these exosomes demonstrated their varying effect on PBMC proliferation, neutrophil survival, and NET formation, highlighting their versatility and broad interaction with immune cells. The knowledge gained from this study will improve our understanding of the miRNA landscape of exosomes from hMSCs and provide a resource for further improving our understanding of exosome cargo and their interaction with immune cells.