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Intravenous and Intratracheal Mesenchymal Stromal Cell Injection in a Mouse Model of Pulmonary Emphysema

机译:肺气肿小鼠模型的静脉和气管内间质基质细胞注射

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摘要

The aim of this study was to characterize the evolution of lung function and -structure in elastase-induced emphysema in adult mice and the effect of mesenchymal stromal cell (MSC) administration on these parameters. Adult mice were treated with intratracheal (4.8 units/100 g bodyweight) elastase to induce emphysema. MSCs were administered intratracheally or intravenously, before or after elastase injection. Lung function measurements, histological and morphometric analysis of lung tissue were performed at 3 weeks, 5 and 10 months after elastase and at 19, 20 and 21 days following MSC administration. Elastase-treated mice showed increased dynamic compliance and total lung capacity, and reduced tissue-specific elastance and forced expiratory flows at 3 weeks after elastase, which persisted during 10 months follow-up. Histology showed heterogeneous alveolar destruction which also persisted during long-term follow-up. Jugular vein injection of MSCs before elastase inhibited deterioration of lung function but had no effects on histology. Intratracheal MSC treatment did not modify lung function or histology. In conclusion, elastase-treated mice displayed persistent characteristics of pulmonary emphysema. Jugular vein injection of MSCs prior to elastase reduced deterioration of lung function. Intratracheal MSC treatment had no effect on lung function or histology.
机译:这项研究的目的是表征成年小鼠肺功能和弹性蛋白酶诱导的肺气肿的结构演变以及间充质基质细胞(MSC)给药对这些参数的影响。成年小鼠经气管内(4.8单位/ 100克体重)弹性蛋白酶处理,诱发肺气肿。在弹性蛋白酶注射之前或之后,通过气管内或静脉内施用MSC。在弹性蛋白酶后3周,5和10个月以及MSC施用后19、20和21天进行肺功能测量,肺组织的组织学和形态计量学分析。弹性蛋白酶处理的小鼠在弹性蛋白酶后3周表现出增加的动态顺应性和总肺活量,并降低了组织特异性弹性和强迫呼气流量,并在10个月的随访期间持续存在。组织学显示异质性肺泡破坏,在长期随访中也持续存在。弹性蛋白酶前颈静脉注射MSCs可抑制肺功能恶化,但对组织学无影响。气管内MSC治疗未改变肺功能或组织学。总之,用弹性蛋白酶处理的小鼠表现出肺气肿的持续特征。在弹性蛋白酶之前颈静脉注射MSC可以减少肺功能的恶化。气管内MSC治疗对肺功能或组织学无影响。

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