|国家科技期刊平台
首页|期刊导航|军事医学|牙髓干细胞预防大鼠高原肺水肿的实验研究

牙髓干细胞预防大鼠高原肺水肿的实验研究OACSTPCD

Protective effect of dental pulp stem cells against high-altitude pulmonary edema in rats

中文摘要英文摘要

目的 评价牙髓干细胞(DPSC)对高原肺水肿(HAPE)的预防作用并初步探讨其作用机制.方法 Sprague-Dawley大鼠21只,随机分为正常对照组(Control)、高原肺水肿组(HAPE)和DPSC预防组(DPSC).模拟高原环境前3d和前Id,DPSC组大鼠尾静脉注射DPSC,Control组和HAPE组尾静脉注射相同体积的磷酸盐缓冲液(PBS).将HAPE组和DPSC组大鼠置于低压低氧模拟舱内,模拟海拔6000 m环境,建立大鼠HAPE模型.3 d后对各组大鼠解剖,制作肺组织切片,苏木精-伊红(HE)染色观察肺组织病理学变化;记录大鼠肺干/湿重;BCA法检测肺组织匀浆总蛋白浓度;实时荧光定量PCR(RT-PCR)和Western印迹检测肺组织水通道蛋白1(APQ-1)表达;比色法和酶联免疫吸附试验(ELISA)检测血浆血管活性物质浓度;ELISA法和RT-PCR法分别检测血清和肺组织炎症因子的表达.结果 低压低氧环境处理3 d,HAPE组大鼠肺内炎细胞浸润增加、肺泡壁增厚、肺泡间质水肿、渗出增多,DPSC预防可显著减轻肺脏的组织病理学损伤.HAPE组大鼠的肺水含量(LWC)和肺组织匀浆总蛋白含量显著升高,DPSC预防组可显著降低LWC和肺组织匀浆总蛋白,二者之间差异具有统计学意义(P<0.01).HAPE组肺组织中AQP-1蛋白与核酸表达水平显著降低,DPSC预防可增强AQP-1在肺组织的表达.HAPE组血浆扩血管活性物质一氧化氮(NO)和前列环素(PGI2)显著降低,而DPSC预防可显著升高血浆扩血管活性物质的表达.HAPE组血清和肺组织炎症因子白细胞介素-1α(IL-1α)和肿瘤坏死因子α(TNF-α)表达显著升高,DPSC组血清和肺组织炎症因子表达显著降低.结论 DPSC可通过促进水通道蛋白表达和提高血浆扩血管物质的含量,以及降低血清及肺组织炎症因子表达,从而预防大鼠高原肺水肿的发生.

Objective To evaluate the protective effect of dental pulp stem cells(DPSCs)against high-altitude pulmonary edema(HAPE)and explore the mechanism.Methods Twenty-one Sprague-Dawley rats were randomly divided into the normal control group(Control),high altitude pulmonary edema group(HAPE)and DPSC prevention group(DPSC).Three days and one day before the hypobaric and hypoxia environment was simulated,DPSCs were administrated via the tail vein in the DPSC group,and phosphate buffered saline(PBS)of the same volume was injected in the control group and HAPE group.After that,rats in the HAPE group and DPSC group were placed in a simulated hypobaric and hypoxic cabin to simulate the environment at an altitude of 6000 m before an HAPE model was established.The rats were sacrificed 3 days later,and the histopathological changes of lung tissue were observed via hematoxylin-eosine(HE)staining.The dry/wet weight of lung tissues was recorded.The concentrations of total protein in lung homogenate were detected using the BCA method.The expression of aquaporin 1(APQ-1)in lung tissue was detected by real-time reverse transcription polymerase chain reaction(RT-PCR)and Western blotting.Colorimetry and enzyme linked immunosorbent assay(ELISA)were used to detect the concentrations of plasma vasoactive substances.The expression of inflammatory factors in serum and lung tissue was detected by ELISA and RT-PCR respectively.Results After three days of treatment in a simulated hypobaric and hypoxic environment,the lung tissue of the HAPE group showed infiltration of inflammatory cells,alveolar wall thickening,alveolar septum thickening and increases of exudation.DPSC prevention could significantly reduce the histopathological damage to the lung.Lung water content(LWC)and total protein content of lung homogenate were significantly increased in the HAPE group but obviously reduced in the DPSC prevention group,and the difference between the two groups was statistically significant(P<0.01).The protein and mRNA expression levels of AQP-1 in lung tissue of the HAPE group were significantly decreased,but prevention via DPSCs could enhance the expression of AQP-1 in lung tissue.In the HAPE group,the concentrations of nitrous oxide(NO)and prostacyclin(PGI2)in plasma were significantly decreased,but prevention via DPSCs could significantly increase the expression of plasma vasoactive substances.The expressions of inflammatory factors interleukin-1 α(IL-1α)and tumor necrosis factor-α(TNF-α)in serum and lung tissue of the HAPE group increased significantly,but decreased in the DPSC prevention group.Conclusion DPSCs can help prevent high-altitude pulmonary edema in rats by promoting the expression of aquaporin,increasing the content of vasodilators in plasma and reducing the expression of inflammatory factors in serum and lung tissue.

李雪;毛壮;王唱垚;王华

安徽医科大学生命科学学院,合肥 230032||军事科学院军事医学研究院,北京 100850军事科学院军事医学研究院,北京 100850军事科学院军事医学研究院,北京 100850||河北大学生命科学学院,河北保定 071002

临床医学

高原肺水肿牙髓干细胞炎症水通道蛋白

high altitude pulmonary edemadental pulp stem cellsinflammationaquaporin

《军事医学》 2024 (007)

495-500 / 6

10.7644/j.issn.1674-9960.2024.07.003

评论