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Journal ArticleDOI

Mesenchymal control of branching pattern in the fetal mouse lung.

S. Robert Hilfer, +2 more
- 01 Jan 1985 - 
- Vol. 17, Iss: 4, pp 523-538
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TLDR
The results indicate that branching pattern is determined by the mesenchyme surrounding the epithelial primordium, however, the capacity to synthesize surfactant isetermined by the source of the epithelium; mesenchYme may control the degree of expression but not the absolute presence or absence of the differentiated condition.
Abstract
The effect of mesenchyme on specialization of respiratory epithelium in the fetal mouse was tested in organ cultures. Heterologous combinations were made between respiratory and non-respiratory lung epithelia and the corresponding mesenchymes. Isolated terminal respiratory buds of fetal mouse lungs were recombined with mesenchyme from chick lung parabronchi, mouse trachea or from the avascular, non-respiratory air sacs of chick lungs. Isolated non-branching chick air sacs were combined with mouse terminal bud mesenchyme or mesenchyme from the respiratory branches of chick lungs. Air sac epithelia branched in a pattern characteristic of the chick lung when combined with chick respiratory mesenchyme and in a pattern characteristic of mouse lung when combined with mouse terminal bud mesenchyme. Mouse terminal bud epithelia did not branch with either mouse tracheal mesenchyme or chick air sac mesenchyme but branched in a chick pattern with chick parabronchial mesenchyme. Electron microscopic examination of the cultures showed that all chick air sac epithelial cultures failed to produce surfactant (lamellar bodies) even when they branched. Control cultures of mouse terminal buds contained large numbers of lamellar bodies; mesenchyme which suppressed branching reduced the number of lamellar bodies to only a few in a small proportion of the cells. Culture medium supplemented with growth factors and hormones increased the number of lamellar bodies in heterologous mouse combinations but did not bring the number to control levels. Supplemented medium had no effect on lamellar body production by chick air sac epithelium. The results indicate that branching pattern is determined by the mesenchyme surrounding the epithelial primordium. However, the capacity to synthesize surfactant is determined by the source of the epithelium; mesenchyme may control the degree of expression but not the absolute presence or absence of the differentiated condition.

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Citations
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Essential role of stromal mesenchyme in kidney morphogenesis revealed by targeted disruption of Winged Helix transcription factor BF-2.

TL;DR: It is suggested that BF-2 controls the production, by the stroma, of signals or factors that are required for the normal transition of induced mesenchyme into tubular epithelium and full growth and branching of the collecting system.
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Alveogenesis failure in PDGF-A-deficient mice is coupled to lack of distal spreading of alveolar smooth muscle cell progenitors during lung development

TL;DR: It is proposed that lung PDGF-Ralpha+ cells are progenitors of the tropoelastin-positive alveolar SMC, and postnatal alveogenesis failure in PD GF-A(-/-) mice is due to a prenatal block in the distal spreading of PDGF+ cells along the tubular lung epithelium during the canalicular stage of lung development.
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Progenitor cells of the adult human airway involved in submucosal gland development.

TL;DR: Evidence is provided for the existence of multiple progenitors in the airway with either limited or pluripotent capacity for differentiation and a novel mechanism of gland morphogenesis by which independently formed glands interact to join glandular lumens.
Journal ArticleDOI

Epigenetic role of epidermal growth factor expression and signalling in embryonic mouse lung morphogenesis.

TL;DR: It is concluded that early mouse embryo lungs express EGF transcripts and corresponding EGF peptides in a specific position-restricted distribution which coimmunolocalizes with EGFR in the primitive airways, while stimulatory and inhibitory studies indicate a functional role for the transduced EGF signal in the epigenetic regulation of lung branching morphogenesis.
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Pulmonary malformation in transgenic mice expressing human keratinocyte growth factor in the lung.

TL;DR: It appears that precise temporal and spatial expression of KGF is likely to play a crucial role in the control of branching morphogenesis during fetal lung development.
References
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Mesenchyme-dependent morphogenesis and epithelium-specific cytodifferentiation in mouse mammary gland

TL;DR: Isografts of heterotypic recombinants of embryonic mammary epithelium with salivary mesenchyme undergo development morphogenetically resembling that of Salivary gland, however, cytodifferentiation of the epithelia is like that of mammary gland.
Journal ArticleDOI

Organ specificity in mesenchymal induction demonstrated in the embryonic development of the mammary gland of the mouse.

TL;DR: Mammary gland rudiments of 12- to 14-day mouse embryos developed typically in organ culture, forming a nipple with a nipple sheath, a ramifying duct system, and adipose tissue, while rudiments taken from 16-day embryos failed to develop under the same culture conditions.
Journal ArticleDOI

Mammalian lung development: Interactions in formation and morphogenesis of tracheal buds

TL;DR: Thymidine labeling experiments fail to provide evidence that differential mitotic activity leads to initial bud formation, and bronchial mesoderm is required if the latter morphogenetic process is to occur.
Journal ArticleDOI

Mammalian lung development: Interactions in primordium formation and bronchial morphogenesis†

TL;DR: The results reveal two levels of mesodermal control of lung development: Interactions between nonspecific mesoderm and gut endoderm result in lung bud formation, while those between specific bronchial mesmoderm and bud endODerm are required for branching morphogenesis.
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