Niedermaier Sophie, Hilgendorff Anne
Comprehensive Pneumology Center (CPC), Helmholtz Zentrum München, Member of the German Center for Lung Research (DZL), Munich Max-Lebsche-Platz 31, 81377, Munich, Germany.
Dr. von Hauner Children's Hospital, Ludwig-Maximilians University Munich, Munich, Germany.
Mol Cell Pediatr. 2015 Dec;2(1):2. doi: 10.1186/s40348-015-0013-7. Epub 2015 Feb 26.
Neonatal chronic lung disease in the preterm infant, i.e. bronchopulmonary dysplasia (BPD) is characterized by impaired pulmonary development with its effects persisting into adulthood. Triggered in the immature lung by infectious complications, oxygen toxicity and the impact of mechanical ventilation, a sustained inflammatory response, extensive remodeling of the extracellular matrix, increased apoptosis as well as altered growth factor signaling characterize the disease. The current review focuses on selected pathophysiologic processes and their interplay in disease development. Furthermore, the potential of both, acute and long-term changes to the pulmonary scaffold and the cellular interface in concert with dysregulated growth factor signaling to affect aging and repair processes in the adult lung is discussed.
早产儿的新生儿慢性肺部疾病,即支气管肺发育不良(BPD),其特征是肺部发育受损,且这种影响会持续到成年期。由感染并发症、氧中毒和机械通气的影响引发于未成熟肺中,持续的炎症反应、细胞外基质的广泛重塑、细胞凋亡增加以及生长因子信号改变是该疾病的特征。本综述聚焦于疾病发展过程中选定的病理生理过程及其相互作用。此外,还讨论了肺部支架和细胞界面的急性和长期变化与失调的生长因子信号协同作用对成年肺的衰老和修复过程产生影响的可能性。