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出生后和肺切除后肺生长的比较基因表达谱。

Comparative gene expression profiling of post-natal and post-pneumonectomy lung growth.

机构信息

Max-Planck-Institute for Heart and Lung Research, Bad Nauheim, Germany.

出版信息

Eur Respir J. 2010 Mar;35(3):655-66. doi: 10.1183/09031936.00059709. Epub 2009 Aug 28.

DOI:10.1183/09031936.00059709
PMID:19717484
Abstract

Although increasing numbers of patients suffer from chronic destructive lung diseases, there are no effective therapeutic options apart from transplantation. Understanding the mechanisms of physiological and regenerative alveolar septation is prerequisite for the development of regenerative therapies for the lung. We compared lung gene expression in the phase of induction of post-natal and post-pneumonectomy alveolarisation to identify regulatory genes involved in both processes. We performed genome-wide microarray screenings of newborn and pneumonectomised mouse lungs 1 and 3 days after birth or surgery. Selected candidates were validated by real-time PCR, Western blot and in situ hybridisation. We found 58 genes to be regulated in both models with 40 candidates being changed likewise. Many of these genes participated in growth and differentiation processes. Additionally, immune system, structural molecules, respiratory chain, signal transduction and metabolism were involved. Some candidates were not yet linked to specific functions. The highest regulatory concordance was observed for various isoforms of (pro-)collagen molecules, elastin and the elastin-associated protein fibrillin1 being corporately upregulated. Our findings do not definitively support a common regulating mechanism for induction of post-natal and adult alveolarisation, but some candidates in the intersection of both models are promising for further investigations.

摘要

尽管越来越多的患者患有慢性破坏性肺部疾病,但除了移植之外,尚无有效的治疗选择。了解生理和再生肺泡分隔的机制是开发肺部再生疗法的前提。我们比较了诱导出生后和肺切除术后肺泡化过程中的肺基因表达,以鉴定参与这两个过程的调节基因。我们对出生后 1 天和 3 天的新生和肺切除的小鼠肺进行了全基因组微阵列筛选。通过实时 PCR、Western blot 和原位杂交验证了选定的候选物。我们发现 58 个基因在两种模型中均受到调节,其中 40 个候选物同样发生变化。这些基因中的许多参与了生长和分化过程。此外,免疫系统、结构分子、呼吸链、信号转导和代谢也参与其中。一些候选物尚未与特定功能相关联。观察到各种(原)胶原蛋白分子、弹性蛋白和弹性蛋白相关蛋白原纤维蛋白 1 的各种同工型的最高调节一致性,它们共同上调。我们的研究结果并不完全支持诱导出生后和成人肺泡化的共同调节机制,但两个模型交叉点的一些候选物具有进一步研究的潜力。

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