The molecular basis for abnormal human lung development

被引:47
作者
Groenman, F
Unger, S
Post, M
机构
[1] Univ Toronto, Hosp Sick Children, Res Inst, Dept Pediat,Program Lung Biol Res, Toronto, ON M5G 1X8, Canada
[2] Univ Toronto, Mt Sinai Hosp, Toronto, ON M5G 1X5, Canada
来源
BIOLOGY OF THE NEONATE | 2005年 / 87卷 / 03期
关键词
lung development; cell-cell signaling; neonatal lung disease;
D O I
10.1159/000082595
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Our understanding of lung development in the past two decades has moved from an anatomical to a histological basis and, most recently, to a molecular basis. Tissue interactions specify tracheal and lung primordia formation, program branching morphogenesis of the airway epithelium and regulate epithelial differentiation. In addition, lung development is influenced by mechanical and humoral factors. The regulatory molecules involved in morphogenetic signaling include growth and transcription factors and extracellular matrix molecules. These morphogenetic signals are responsible for lung patterning and differentiation. We will provide a brief overview of molecular signaling during early respiratory formation, airway branching, pulmonary vascularization and epithelial differentiation. We will then review aberrant morphogenetic signaling in human lung abnormalities, such as tracheoesophageal fistula, congenital diaphragmatic hernia, pulmonary hyperplasia, alveolar capillary dysplasia, congenital cystic adenomatoid malformation and bronchopulmonary dysplasia. Copyright (C) 2005 S. Karger AG, Basel.
引用
收藏
页码:164 / 177
页数:14
相关论文
共 173 条
[1]   Bronchopulmonary dysplasia - "A vascular hypothesis" [J].
Abman, SH .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2001, 164 (10) :1755-1756
[2]   Temporal and spatial regulation of VEGF-A controls vascular patterning in the embryonic lung [J].
Akeson, AL ;
Greenberg, JM ;
Cameron, JE ;
Thompson, FY ;
Brooks, SK ;
Wiginton, D ;
Whitsett, JA .
DEVELOPMENTAL BIOLOGY, 2003, 264 (02) :443-455
[3]   Notch signaling: Cell fate control and signal integration in development [J].
Artavanis-Tsakonas, S ;
Rand, MD ;
Lake, RJ .
SCIENCE, 1999, 284 (5415) :770-776
[4]   Early postnatal lethality in Hoxa-5 mutant mice is attributable to respiratory tract defects [J].
Aubin, J ;
Lemieux, M ;
Tremblay, M ;
Bérard, J ;
Jeannotte, L .
DEVELOPMENTAL BIOLOGY, 1997, 192 (02) :432-445
[5]   Reductions in the incidence of nitrofen-induced diaphragmatic hernia by vitamin A and retinoic acid [J].
Babiuk, RP ;
Thébaud, B ;
Greer, JJ .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2004, 286 (05) :L970-L973
[6]   Diaphragm defects occur in a CDH hernia model independently of myogenesis and lung formation [J].
Babiuk, RP ;
Greer, JJ .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2002, 283 (06) :L1310-L1314
[7]  
Bellusci S, 1997, DEVELOPMENT, V124, P53
[8]   Pathogenesis, pathology and pathophysiology of pulmonary sequelae of bronchopulmonary dysplasia in premature infants [J].
Bhandari, A ;
Bhandari, V .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2003, 8 :E370-E380
[9]   Disrupted pulmonary vasculature and decreased vascular endothelial growth factor, Flt-1, and TIE-2 in human infants dying with bronchopulmonary dysplasia [J].
Bhatt, AJ ;
Pryhuber, GS ;
Huyck, H ;
Watkins, RH ;
Metlay, LA ;
Maniscalco, WM .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2001, 164 (10) :1971-1980
[10]   IDENTIFICATION OF HEPATOCYTE NUCLEAR FACTOR-III BINDING-SITES IN THE CLARA CELL SECRETORY PROTEIN GENE [J].
BINGLE, CD ;
GITLIN, JD .
BIOCHEMICAL JOURNAL, 1993, 295 :227-232