Zhang Lichun, Li Qiuhe, Liu Zhenning, Wang Yu, Zhao Min
Department of Emergency, Shengjing Hospital Affiliated to China Medical University No. 36 Sanhao Street, Heping District, Shenyang 110004, Liaoning Province, China.
Am J Transl Res. 2019 Jun 15;11(6):3707-3721. eCollection 2019.
To evaluate the protective effect of bone mesenchymal stem cells (BMSCs) on paraquat (PQ)-induced acute lung injury (ALI) and investigate the possible underlying mechanisms.
Male Sprague Dawley rats were treated with BMSCs (3 × 10) 1 h after intraperitoneal injection of PQ. The cell apoptosis rate and mitochondrial membrane potential in rat pulmonary alveolar type II epithelial (ATII) cells were quantitated by flow cytometry. IL-17, IL-6, and MUC5B levels in bronchoalveolar lavage fluid (BALF) and ATII culture medium were measured. Lung tissues were collected to determine the wet-to-dry (W/D) ratios and lung injury scores, in addition to the protein and mRNA expression levels of ERK1/2, Bcl-2, Bax, and muc5b.
BMSCs had decreased mRNA expression of Muc5b in lung tissue of rats with PQ-induced ALI as shown by RNA-seq. Treatment with BMSCs also alleviated the PQ-induced increases in protein expression in the BALF and reduced the concentration of IL-17, IL-6, and Muc5b in both the BALF and ATII culture medium. In addition, the ATII cell apoptosis rate and mitochondrial membrane potential, as well as the W/D ratios, were decreased by BMSC treatment. Moreover, BMSCs ameliorated the expression levels of mRNA and active caspase-3 proteins and increased mRNA expression. Furthermore, BMSCs attenuated ERK1/2 activation upon PQ-induced ALI in lung tissue.
BMSC therapy can protect against PQ-induced ALI in rats. A possible mechanism is the suppression of the muc5b and ERK/MAPK signaling pathways, resulting in an improvement in the endothelial permeability and a decrease in inflammation and cell apoptosis.
评估骨髓间充质干细胞(BMSCs)对百草枯(PQ)诱导的急性肺损伤(ALI)的保护作用,并探讨其可能的潜在机制。
雄性Sprague Dawley大鼠在腹腔注射PQ 1小时后接受BMSCs(3×10)治疗。通过流式细胞术定量大鼠肺泡II型上皮(ATII)细胞中的细胞凋亡率和线粒体膜电位。测量支气管肺泡灌洗液(BALF)和ATII培养基中IL-17、IL-6和MUC5B的水平。收集肺组织以确定湿干(W/D)比值和肺损伤评分,以及ERK1/2、Bcl-2、Bax和muc5b的蛋白质和mRNA表达水平。
RNA测序显示,BMSCs降低了PQ诱导的ALI大鼠肺组织中Muc5b的mRNA表达。BMSCs治疗还减轻了PQ诱导的BALF中蛋白质表达的增加,并降低了BALF和ATII培养基中IL-17、IL-6和Muc5b的浓度。此外,BMSC治疗降低了ATII细胞凋亡率和线粒体膜电位,以及W/D比值。此外,BMSCs改善了mRNA和活性caspase-3蛋白的表达水平,并增加了mRNA表达。此外,BMSCs减弱了肺组织中PQ诱导的ALI时ERK1/2的激活。
BMSC治疗可保护大鼠免受PQ诱导的ALI。一种可能的机制是抑制muc5b和ERK/MAPK信号通路,从而改善内皮通透性,减少炎症和细胞凋亡。