Therapeutic effects of mesenchymal stem cell-derived microvesicles on pulmonary arterial hypertension in rats

• Published in: Acta pharmacologica Sinica Vol. 35; no. 9; pp. 1121 - 1128
• Main Authors: Chen, Jian-ying, An, Ran, Liu, Zhen-jun, Wang, Jin-ju, Chen, Shu-zhen, Hong, Mian-ming, Liu, Jing-hu, Xiao, Meng-yuan, Chen, Yan-fang
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 01.09.2014; Nature Publishing Group
• Subjects: Animals; Biomedical and Life Sciences; Biomedicine; Cell-Derived Microparticles - physiology; Cells, Cultured; Heart Ventricles - physiopathology; Hypertension, Pulmonary - physiopathology; Hypertension, Pulmonary - therapy; Immunology; Internal Medicine; Medical Microbiology; Mesenchymal Stromal Cells - physiology; Original; original-article; Pharmacology/Toxicology; Pulmonary Artery - physiology; Rats; Rats, Sprague-Dawley; SD大鼠; Vaccine; 微泡; 条件培养基; 治疗效果; 肺动脉高压; 透射电子显微镜; 间充质干细胞; 静脉注射; chronic heart disease; microvesicle; pulmonary artery hypertension; stem cell therapy; bone marrow mesenchymal stem cell
• ISSN: 1671-4083; 1745-7254; 1745-7254
• DOI: 10.1038/aps.2014.61

Aim： Microvesicles （MVs） are nanoscale membrane fragments released from virtually all cell types upon activation or apoptosis, and may contribute to the beneficial effects of stem cell therapy. In this study, we investigated the therapeutic effects of mesenchymal stem cell （MSC） derived MVs （MSC-MVs） on pulmonary artery hypertension （PAH） in rats. Methods： MSC-MVs were isolated from rat bone marrow MSCs that were cultured in a serum-free conditioned medium. Transmission electron microscopy （TEM）, flow cytometry and nanoparticle tracking analysis （NTA） were used to characterize the MVs. Adult SD rats were injected with monocrotaline （50 mg/kg, sc） to induce PAH. Three weeks later, the rats were intravenously injected with MSCs, MSC-MVs or saline for 2 weeks. At the end of treatments, the hemodynamic parameters and pathological right ventricular and pulmonary arterial remodeling were analyzed in each group. Results： The MSC-MVs showed general morphologic characteristics of MVs and expressed annexin V and CD29 markers under TEM, and their size ranged from 40 to 300 nm. Intravenous injection of MSC-MVs or MSCs significantly ameliorated the mean pulmonary artery pressure （mPAP） and mean right ventricle pressure （mRVP） in PAH rats. Furthermore, intravenous injection of MSC-MVs or MSCs significantly decreased the right ventricle （RV） hypertrophy and pulmonary arteriole area index （AI） and thickness index （TI） in PAH rats. Conclusion： Intravenous injection of MSC-MVs or MSCs produces similar beneficial effects for treating PAH, and our results provide a basis for cell-free approach in stem cell therapy.