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@ARTICLE{Woik:127808,
author = {N. Woik$^*$ and J. Kroll$^*$},
title = {{R}egulation of lung development and regeneration by the
vascular system.},
journal = {Cellular and molecular life sciences},
volume = {72},
number = {14},
issn = {1420-9071},
address = {Basel},
publisher = {Birkhäuser},
reportid = {DKFZ-2017-03830},
pages = {2709 - 2718},
year = {2015},
abstract = {Blood vessels have been described a long time ago as
passive circuits providing sufficient blood supply to ensure
proper distribution of oxygen and nutrition. Blood vessels
are mainly formed during embryonic development and in the
early postnatal period. In the adult, blood vessels are
quiescent, but can be activated and subsequently induced
under pathophysiological conditions, such as ischemia and
tumor growth. Surprisingly, recent data have suggested an
active function for blood vessels, named angiocrine
signaling, releasing trophogens which regulate organ
development and organ regeneration including in the
pancreas, lung, tumor cells, liver and bone. Lung
development is driven by hypoxia as well as an intense
endothelial-epithelial interaction, and important mechanisms
contributing to these processes have recently been
identified. This review aims to summarize recent
developments and concepts about embryonic pulmonary vascular
development and lung regeneration. We discuss
hypoxia-inducible factor HIF-2α and vascular endothelial
growth factor VEGF as important mediators in lung
development and focus on endothelial-epithelial interactions
and angiocrine signaling mechanisms.},
keywords = {Basic Helix-Loop-Helix Transcription Factors (NLM
Chemicals) / Vascular Endothelial Growth Factor A (NLM
Chemicals) / endothelial PAS domain-containing protein 1
(NLM Chemicals)},
cin = {A190},
ddc = {570},
cid = {I:(DE-He78)A190-20160331},
pnm = {321 - Basic Concepts (POF3-321)},
pid = {G:(DE-HGF)POF3-321},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:25894695},
doi = {10.1007/s00018-015-1907-1},
url = {https://inrepo02.dkfz.de/record/127808},
}