Thébaud Bernard
Vascular Biology Group, Division of Neonatology, Department of Pediatrics, University of Alberta, Edmonton, Alta., Canada.
Neonatology. 2007;91(4):291-7. doi: 10.1159/000101344. Epub 2007 Jun 7.
Since the initial description of bronchopulmonary dysplasia (BPD) 40 years ago, advances in perinatal care have allowed the survival of infants that are more immature. The disease has not disappeared, but it now affects infants with undeveloped distal airspaces, resulting in an arrest of alveolar development. The histological changes that occur during normal lung development are well described, but little is known about the signaling mechanisms that regulate saccular and alveolar development. Understanding how alveoli and the underlying capillary network develop and how these mechanisms are disrupted in preterm infants with BPD is critical to develop efficient and effective therapies for lung diseases characterized by alveolar damage. This brief review focuses on the recently recognized role of angiogenic growth factors during normal alveolar development, injury and repair with a particular emphasis on the vascular endothelial growth factor.
自40年前首次描述支气管肺发育不良(BPD)以来,围产期护理的进步使更不成熟的婴儿得以存活。这种疾病并未消失,但现在影响的是远端气腔未发育的婴儿,导致肺泡发育停滞。正常肺发育过程中发生的组织学变化已有详细描述,但对于调节囊状和肺泡发育的信号机制却知之甚少。了解肺泡及潜在的毛细血管网络如何发育,以及这些机制在患有BPD的早产儿中是如何被破坏的,对于开发针对以肺泡损伤为特征的肺部疾病的有效治疗方法至关重要。这篇简短的综述重点关注血管生成生长因子在正常肺泡发育、损伤和修复过程中最近被认识到的作用,尤其着重于血管内皮生长因子。