PDGF-A signaling is a critical event in lung alveolar myofibroblast development and alveogenesis

被引:642
作者
Bostrom, H
Willetts, K
Pekny, M
Leveen, P
Lindahl, P
Hedstrand, H
Pekna, M
Hellstrom, M
GebreMedhin, S
Schalling, M
Nilsson, M
Kurland, S
Tornell, J
Heath, JK
Betsholtz, C
机构
[1] GOTHENBURG UNIV,DEPT PHYSIOL,S-41390 GOTHENBURG,SWEDEN
[2] UNIV BIRMINGHAM,SCH BIOCHEM,BIRMINGHAM B15 2TT,W MIDLANDS,ENGLAND
[3] UNIV OXFORD,DEPT BIOCHEM,OXFORD OX1 3QU,ENGLAND
[4] KAROLINSKA HOSP,DEPT MOLEC MED,NEUROGENET UNIT,S-17176 STOCKHOLM,SWEDEN
关键词
D O I
10.1016/S0092-8674(00)81270-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A mouse platelet-derived growth factor A chain (PDGF-A) null allele is shown to be homozygous lethal, with two distinct restriction points, one prenatally before E10 and one postnatally. Postnatally surviving PDGF-A-deficient mice develop lung emphysema secondary to the failure of alveolar septation. This is apparently caused by the loss of alveolar myofibroblasts and associated elastin fiber deposits. PDGF alpha receptor-positive cells in the lung having the location of putative alveolar myofibroblast progenitors were specifically absent in PDGF-A null mutants. We conclude that PDGF-A is crucial for alveolar myofibroblast ontogeny. We have previously shown that PDGF-B is required in the ontogeny of kidney mesangial cells. The PDGFs therefore appear to regulate the generation of specific populations of myofibroblasts during mammalian development. The two PDGF null phenotypes also reveal analogous morphogenetic functions for myofibroblast-type cells in lung and kidney organogenesis.
引用
收藏
页码:863 / 873
页数:11
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