Aberrant Pulmonary Vascular Growth and Remodeling in Bronchopulmonary Dysplasia

被引:65
作者
Alvira, Cristina M. [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Pediat, Div Crit Care Med, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
pulmonary angiogenesis; pulmonary hypertension; alveolarization; chronic lung disease; VEGF; HIF; nitric oxide; NITRIC-OXIDE SYNTHASE; CHRONIC LUNG-DISEASE; HYPOXIA-INDUCIBLE FACTORS; ENDOTHELIAL PROGENITOR CELLS; MESENCHYMAL STEM-CELLS; PRETERM INFANTS; LYSOPHOSPHATIDIC ACID; RESPIRATORY-DISTRESS; ARTERY HYPERTENSION; HISTOLOGIC EVIDENCE;
D O I
10.3389/fmed.2016.00021
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In contrast to many other organs, a significant portion of lung development occurs after birth during alveolarization, thus rendering the lung highly susceptible to injuries that may disrupt this developmental process. Premature birth heightens this susceptibility, with many premature infants developing the chronic lung disease, bronchopulmonary dysplasia (BPD), a disease characterized by arrested alveolarization. Over the past decade, tremendous progress has been made in the elucidation of mechanisms that promote postnatal lung development, including extensive data suggesting that impaired pulmonary angiogenesis contributes to the pathogenesis of BPD. Moreover, in addition to impaired vascular growth, patients with BPD also frequently demonstrate alterations in pulmonary vascular remodeling and tone, increasing the risk for persistent hypoxemia and the development of pulmonary hypertension. In this review, an overview of normal lung development will be presented, and the pathologic features of arrested development observed in BPD will be described, with a specific emphasis on the pulmonary vascular abnormalities. Key pathways that promote normal pulmonary vascular development will be reviewed, and the experimental and clinical evidence demonstrating alterations of these essential pathways in BPD summarized.
引用
收藏
页数:14
相关论文
共 145 条
[21]   Mechanical ventilation with 40% oxygen reduces pulmonary expression of genes that regulate lung development and impairs alveolar septation in newborn mice [J].
Bland, Richard D. ;
Mokres, Lucia M. ;
Ertsey, Robert ;
Jacobson, Berit E. ;
Jiang, Shu ;
Rabinovitch, Marlene ;
Xu, Liwen ;
Shinwell, Eric S. ;
Zhang, Feijie ;
Beasley, Matthew A. .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2007, 293 (05) :L1099-L1110
[22]   Circulating Endothelial Progenitor Cells in Preterm Infants with Bronchopulmonary Dysplasia [J].
Borghesi, Alessandro ;
Massa, Margherita ;
Campanelli, Rita ;
Bollani, Lina ;
Tzialla, Chryssoula ;
Figar, Tiziana A. ;
Ferrari, Giovanna ;
Bonetti, Elisa ;
Chiesa, Gaia ;
de Silvestri, Annalisa ;
Spinillo, Arsenio ;
Rosti, Vittorio ;
Stronati, Mauro .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2009, 180 (06) :540-546
[23]   CHANGES IN PULMONARY CIRCULATION IN SEVERE BRONCHOPULMONARY DYSPLASIA [J].
BUSH, A ;
BUSST, CM ;
KNIGHT, WB ;
HISLOP, AA ;
HAWORTH, SG ;
SHINEBOURNE, EA .
ARCHIVES OF DISEASE IN CHILDHOOD, 1990, 65 (07) :739-745
[24]   Abnormal blood vessel development and lethality in embryos lacking a single VEGF allele [J].
Carmeliet, P ;
Ferreira, V ;
Breier, G ;
Pollefeyt, S ;
Kieckens, L ;
Gertsenstein, M ;
Fahrig, M ;
Vandenhoeck, A ;
Harpal, K ;
Eberhardt, C ;
Declercq, C ;
Pawling, J ;
Moons, L ;
Collen, D ;
Risau, W ;
Nagy, A .
NATURE, 1996, 380 (6573) :435-439
[25]   VENTILATOR-RELATED PATHOLOGY IN THE EXTREMELY IMMATURE LUNG [J].
CHAMBERS, HM ;
VANVELZEN, D .
PATHOLOGY, 1989, 21 (02) :79-83
[26]   Mesenchymal Stem Cells for Bronchopulmonary Dysplasia: Phase 1 Dose-Escalation Clinical Trial [J].
Chang, Yun Sil ;
Ahn, So Yoon ;
Yoo, Hye Soo ;
Sung, Se In ;
Choi, Soo Jin ;
Oh, Won Il ;
Park, Won Soon .
JOURNAL OF PEDIATRICS, 2014, 164 (05) :966-+
[27]   Human Umbilical Cord Blood-Derived Mesenchymal Stem Cells Attenuate Hyperoxia-Induced Lung Injury in Neonatal Rats [J].
Chang, Yun Sil ;
Oh, Wonil ;
Choi, Soo Jin ;
Sung, Dong Kyung ;
Kim, Soo Yoon ;
Choi, Eun Yang ;
Kang, Saem ;
Jin, Hye Jin ;
Yang, Yoon Sun ;
Park, Won Soon .
CELL TRANSPLANTATION, 2009, 18 (08) :869-886
[28]   Deficiency or inhibition of lysophosphatidic acid receptor 1 protects against hyperoxia-induced lung injury in neonatal rats [J].
Chen, X. ;
Walther, F. J. ;
van Boxtel, R. ;
Laghmani, E. H. ;
Sengers, R. M. A. ;
Folkerts, G. ;
DeRuiter, M. C. ;
Cuppen, E. ;
Wagenaar, G. T. M. .
ACTA PHYSIOLOGICA, 2016, 216 (03) :358-375
[29]   Deferoxamine Improves Alveolar and Pulmonary Vascular Development by Upregulating Hypoxia-inducible Factor-1α in a Rat Model of Bronchopulmonary Dysplasia [J].
Choi, Chang Won ;
Lee, Juyoung ;
Lee, Hyun Ju ;
Park, Hyoung-Sook ;
Chun, Yang-Sook ;
Kim, Beyong Il .
JOURNAL OF KOREAN MEDICAL SCIENCE, 2015, 30 (09) :1295-1301
[30]   LPA Receptors: Subtypes and Biological Actions [J].
Choi, Ji Woong ;
Herr, Deron R. ;
Noguchi, Kyoko ;
Yung, Yun C. ;
Lee, Charig-Wook ;
Mutoh, Tetsuji ;
Lin, Mu-En ;
Teo, Siew T. ;
Park, Kristine E. ;
Mosley, Alycia N. ;
Chun, Jerold .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 2010, 50 :157-186