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Mesenchymal stromal cells facilitate resolution of pulmonary fibrosis by miR-29c and miR-129 intercellular transfer Full article

Journal Experimental and Molecular Medicine
ISSN: 1226-3613 , E-ISSN: 2092-6413
Output data Year: 2023, Volume: 55, Number: 7, Pages: 1399-1412 Pages count : 14 DOI: 10.1038/s12276-023-01017-w
Authors Basalova Nataliya 1 , Arbatskiy Mikhail 2 , Popov Vladimir 1,2 , Grigorieva Olga 1 , Vigovskiy Maksim 1,2 , Zaytsev Ivan 2 , Novoseletskaya Ekaterina 1 , Sagaradze Georgy 1,2 , Danilova Natalia 2 , Malkov Pavel 2,3 , Cherniaev Andrey 4,5 , Samsonova Maria 4,5 , Karagyaur Maxim 1,2 , Tolstoluzhinskaya Anastasiya 1,2 , Dyachkova Uliana 2 , Akopyan Zhanna 1,2 , Tkachuk Vsevolod 2 , Kalinina Natalia 2 , Efimenko Anastasiya 1,2
Affiliations
1 Institute for Regenerative Medicine, Medical Research and Education Center, Lomonosov Moscow State University, Moscow, Russian Federation
2 Faculty of Medicine, Lomonosov Moscow State University, Moscow, Russian Federation
3 Department of Clinical Pathology, Medical Research and Education Centre, Lomonosov Moscow State University, Moscow, Russian Federation
4 Division of Fundamental Medicine of Federal State Budgetary Institution "Pulmonology Scientific Research Institute under Federal Medical and Biological Agency of Russian Federation", Moscow, Russian Federation
5 Research Institute of Human Morphology, Moscow, Russian Federation

Abstract: To date, pulmonary fibrosis remains an unmet medical need. In this study, we evaluated the potency of mesenchymal stromal cell (MSC) secretome components to prevent pulmonary fibrosis development and facilitate fibrosis resolution. Surprisingly, the intratracheal application of extracellular vesicles (MSC-EVs) or the vesicle-depleted secretome fraction (MSC-SF) was not able to prevent lung fibrosis when applied immediately after the injury caused by bleomycin instillation in mice. However, MSC-EV administration induced the resolution of established pulmonary fibrosis, whereas the vesicle-depleted fraction did not. The application of MSC-EVs caused a decrease in the numbers of myofibroblasts and FAPa+ progenitors without affecting their apoptosis. Such a decrease likely occurred due to their dedifferentiation caused by microRNA (miR) transfer by MSC-EVs. Using a murine model of bleomycin-induced pulmonary fibrosis, we confirmed the contribution of specific miRs (miR-29c and miR-129) to the antifibrotic effect of MSC-EVs. Our study provides novel insights into possible antifibrotic therapy based on the use of the vesicle-enriched fraction of the MSC secretome.
Cite: Basalova N. , Arbatskiy M. , Popov V. , Grigorieva O. , Vigovskiy M. , Zaytsev I. , Novoseletskaya E. , Sagaradze G. , Danilova N. , Malkov P. , Cherniaev A. , Samsonova M. , Karagyaur M. , Tolstoluzhinskaya A. , Dyachkova U. , Akopyan Z. , Tkachuk V. , Kalinina N. , Efimenko A.
Mesenchymal stromal cells facilitate resolution of pulmonary fibrosis by miR-29c and miR-129 intercellular transfer
Experimental and Molecular Medicine. 2023. V.55. N7. P.1399-1412. DOI: 10.1038/s12276-023-01017-w OpenAlex
Dates:
Submitted: Dec 19, 2022
Accepted: Mar 26, 2023
Published online: Jul 3, 2023
Identifiers:
OpenAlex: W4382895238
Citing:
DB Citing
OpenAlex 32
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