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Effects of postnatal dexamethasone treatment on mRNA expression profiles of genes related to alveolar development in an emphysema model in mice

机译:产后地塞米松对肺气肿模型小鼠肺泡发育相关基因mRNA表达谱的影响

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Emphysema can be induced in animals by postnatal treatment with dexamethasone (Dex) and such models have been widely used for various research. However, it is not clear what are the effects of Dex on assembly of alveolar elastic fibers in the emphysema model in mice. This study compared the expression profile of genes related to alveolar development between Dex treated and control mice during the treatment from postnatal day 3 (P3) to P14 with a 2-day break. From morphological observation of lung sections on P42, we confirmed the induction of emphysema in the treated mice. The mRNA expression level of fibrillin-1, which consists of microfibrils as a scaffold to form elastic fibers, and fibulin-5, which is a key protein reinforcing the fibers, reached maximum on P7 in control mice. However, in the Dex group, expression levels both types of mRNA were much lower with no clear expression peak. On the other hand, mRNA expression of tropoelastin, the main component in elastic fibers, reached maximum on P5 in the Dex group, which was 9 days earlier than in the control group. At this time, the amount of microfibrils might not be enough for tropoelastin to be deposited completely in Dex treated mice. This imbalance in the expression of tropoelastin and microfibril might interfere with the efficient formation of elastic fibers.
机译:产后用地塞米松(Dex)治疗可诱发动物气肿,这种模型已广泛用于各种研究。但是,尚不清楚Dex对小鼠气肿模型中肺泡弹性纤维组装的影响是什么。这项研究比较了在出生后第3天(P3)至P14休息2天期间,接受Dex治疗的小鼠和对照小鼠之间与肺泡发育相关的基因的表达谱。从P42肺部的形态学观察,我们证实了在治疗小鼠中诱发了肺气肿。在对照小鼠的P7上,由微纤维构成支架以形成弹性纤维的fibrillin-1的mRNA表达水平和作为增强纤维的关键蛋白质的fibrinin-5的mRNA表达水平达到了最大值。然而,在Dex组中,两种类型的mRNA的表达水平都低得多,没有清晰的表达峰。另一方面,弹性纤维中主要成分原弹性蛋白的mRNA表达在Dex组的P5上达到最大,比对照组早9天。此时,微原纤维的量可能不足以使原弹性蛋白完全沉积在Dex治疗的小鼠中。原弹性蛋白和微原纤维表达的这种不平衡可能会干扰弹性纤维的有效形成。

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