The Second Hospital, Cheeloo College of Medicine, Shandong University, Shandong, China.
Central Research Laboratory, The Second Hospital, Cheeloo College of Medicine, Shandong University, No. 247, Beiyuan Dajie, Jinan, 250033, China.
Curr Pharm Biotechnol. 2021;22(12):1654-1662. doi: 10.2174/1389201022666201231113127.
Pulmonary arterial Hypertension (PH) is a chronic disease that ultimately progresses to right ventricular failure and death. Until now, there is still a lack of effective treatment applied. The purpose of the present study was to observe the protective effect of Mesenchymal Stromal Cell-Derived Exosomes (MSC-EXO) against experimental Pulmonary arterial Hypertension (PH) and right ventricular failure.
All the experimental rats received an intraperitoneal injection of 50 mg/kg monocrotaline to induce PH model. Three weeks after the model was successfully established, the cell Culture Media (CM) or MSC-EXO derived from human umbilical cord was administered daily via the tail vein. All animals were randomly divided into 4 groups: Control (saline-treated), MCT-PH, MCT-CM and MCT-EXO groups. Post-operation, hemodynamic data and index of right ventricular hypertrophy (RVHI) were recorded to evaluate the inhibition of MSC-EXO on MCT-induced PH. Histology, immunohistochemistry and western blot were used to analyze the effect of MSC-EXO against vascular remodeling and further reveal the mechanism.
In the present study, our results showed that MSC-EXO administration could significantly reduce the Right Ventricular Systolic Pressure (RVSP) and RVHI, suppress the pulmonary vascular remodeling and The Endothelial-Mesenchymal Transition (EndMT) process.
Our results provided the firm information for a new method in the treatment of PH; the mechanism may be related to the inhibition of vascular remodeling and EndMT.
肺动脉高压(PH)是一种慢性疾病,最终会导致右心衰竭和死亡。到目前为止,仍然缺乏有效的治疗方法。本研究的目的是观察间充质干细胞衍生的外泌体(MSC-EXO)对实验性肺动脉高压(PH)和右心衰竭的保护作用。
所有实验大鼠均接受腹腔注射 50mg/kg 野百合碱以诱导 PH 模型。模型建立 3 周后,通过尾静脉每日给予细胞培养基(CM)或来源于人脐带的 MSC-EXO。所有动物随机分为 4 组:对照组(生理盐水处理)、MCT-PH 组、MCT-CM 组和 MCT-EXO 组。术后记录血流动力学数据和右心室肥厚指数(RVHI),以评估 MSC-EXO 对 MCT 诱导的 PH 的抑制作用。组织学、免疫组织化学和 Western blot 用于分析 MSC-EXO 对血管重构的影响,并进一步揭示其机制。
在本研究中,我们的结果表明,MSC-EXO 给药可显著降低右心室收缩压(RVSP)和 RVHI,抑制肺血管重构和内皮-间充质转化(EndMT)过程。
我们的结果为 PH 的治疗提供了新的方法的可靠信息;其机制可能与血管重构和 EndMT 的抑制有关。