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

Författare

  • Hans Ehrencrona
  • Karen Willetts
  • Milos Pekny
  • Per Levéen
  • Per Lindahl
  • Håkan Hedstrand
  • Marcela Pekna
  • Mats Hellström
  • Samuel Gebre-Medhin
  • Martin Schalling
  • Mia Nilsson
  • Siri Kurland
  • Jan Törnell
  • John K Heath
  • Christer Betsholtz

Summary, in English

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.

Publiceringsår

1996

Språk

Engelska

Sidor

863-873

Publikation/Tidskrift/Serie

Cell

Volym

85

Issue

6

Dokumenttyp

Artikel i tidskrift

Förlag

Cell Press

Ämne

  • Medical Genetics

Nyckelord

  • Pulmonary Alveoli
  • Platelet-Derived Growth Factor
  • Phenotype
  • Smooth
  • Muscle
  • Mutant Strains
  • Mice
  • Lung
  • Gene Targeting
  • Fibroblasts
  • Elastin
  • Genetic
  • Crosses
  • Chimera
  • Cardiomegaly
  • Actins
  • Animals
  • Pulmonary Emphysema
  • RNA
  • Messenger
  • Receptor
  • Platelet-Derived Growth Factor alpha
  • Receptors
  • Signal Transduction

Status

Published

ISBN/ISSN/Övrigt

  • ISSN: 1097-4172