Children with congenital diaphragmatic hernia (CDH), a condition characterised by herniation of the abdominal contents into the thoracic cavity, also develop pulmonary hypertension. Angiopoietin-1 (Ang-1), a central mediator of angiogenesis, is involved in the development of non-familial pulmonary hypertension, but its role in CDH-associated pulmonary hypertension is unclear. Grzenda et al. now examine the expression patterns of Ang-1 and its receptor Tie-2 during lung development in normal mice and in a nitrofen-based murine model of CDH. Their results suggest that the Ang-1–Tie-2 pathway is important during normal lung development and that alterations in the pathway might be responsible for the development of pulmonary hypertension in CDH. Investigation of the role of other components of the Ang-1 pathway during normal and pathological lung development is therefore warranted. Page 106
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IN THIS ISSUE| 01 January 2013
Ang-1, lung development and congenital diaphragmatic hernia
Online ISSN: 1754-8411
Print ISSN: 1754-8403
Written by Jane Bradbury. © 2012. Published by The Company of Biologists Ltd.
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial Share Alike License (http://creativecommons.org/licenses/by-nc-sa/3.0), which permits unrestricted non-commercial use, distribution and reproduction in any medium provided that the original work is properly cited and all further distributions of the work or adaptation are subject to the same Creative Commons License terms.
Dis Model Mech (2013) 6 (1): 1.
Ang-1, lung development and congenital diaphragmatic hernia. Dis Model Mech 1 January 2013; 6 (1): 1. doi:
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