Altered Lung Development in Bronchopulmonary Dysplasia

被引:36
|
作者
Hadchouel, Alice [1 ,2 ,3 ]
Franco-Montoya, Marie-Laure [1 ]
Delacourt, Christophe [1 ,2 ,3 ]
机构
[1] Hop Henri Mondor, INSERM, U955, IMRB,Equipe 04, F-94010 Creteil, France
[2] Hop Necker Enfants Malad, AP HP, Serv Pneumol Pediat, Ctr Reference Malad Resp Rares Enfant, F-75015 Paris, France
[3] Univ Paris 05, Paris, France
关键词
preterm; metalloproteinases; VEGF; genetics; airway; alveolarization; lung function; ENDOTHELIAL GROWTH-FACTOR; FIBROBLAST-GROWTH; RAT LUNG; PREMATURE-INFANTS; PRETERM BIRTH; MATRIX METALLOPROTEINASES; DIFFERENTIAL EXPRESSION; MECHANICAL VENTILATION; GELATINASE ACTIVITIES; MORPHOMETRIC-ANALYSIS;
D O I
10.1002/bdra.23237
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Bronchopulmonary dysplasia (BPD) is the main respiratory sequela of extreme prematurity. Its pathophysiology is complex, involving interactions between host and environment, likely to be significantly influenced by genetic factors. Thus, the clinical presentation and histological lesions have evolved over time, along with the reduction in neonatal injuries, and the care of more immature children. Impaired alveolar growth, however, is a lesion consistently observed in BPD, such that it is a key feature in BPD, and is even the dominant characteristic of the so-called new forms of BPD. This review describes the key molecular pathways that are believed to be involved in the genesis of BPD. Much of our understanding is based on animal models, but this is increasingly being enriched by genetic approaches, and long-term respiratory functional studies. Birth Defects Research (Part A) 100:158-167, 2014. (c) 2014 Wiley Periodicals, Inc.
引用
收藏
页码:158 / 167
页数:10
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