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Tenascin-C in rat lung: distribution, ontogeny and role in branching morphogenesis.

Publication ,  Journal Article
Young, SL; Chang, LY; Erickson, HP
Published in: Dev Biol
February 1994

Extracellular matrix is important to organogenesis and may function by modifying cellular adhesion, motility, proliferation, and differentiation. Tenascin-C (TN-C) is a matrix molecule reported to bind some cell lines and to inhibit adhesion of some cell types to fibronectin. This report describes the ontogeny and possible functions of TN-C expression in fetal and newborn rat lung. There was a moderate concentration of TN-C protein at the epithelial-mesenchymal interface during fetal lung development in the period of branching morphogenesis. There was a remarkable accumulation of TN-C during the first postnatal week when alveolarization peaked, followed by a decline to barely detectable levels after the third postnatal week when alveolarization was essentially completed. Loss of TN-C protein followed quickly the loss of TN-C mRNA, suggesting a rapid turnover of TN-C in the extracellular matrix. By light microscopy, immunoreactive TN-C was present in early postnatal lung at the epithelial-mesenchymal interface and was distributed throughout lung mesenchyme. Electron microscopic immunocytochemistry showed TN-C was not a part of the basal lamina and that its lung localization was punctate and different from the uniform distribution of laminin. Antiserum to TN-C significantly inhibited branching morphogenesis of fetal lung explants but did not block their growth. Three bacterially expressed segments of TN-C comprising different fibronectin type III domains inhibited branching morphogenesis as effectively as did antiserum, but an expression protein of the carboxyterminal fibrinogen-like segment had no effect. We conclude that TN-C is expressed in a spatio-temporal pattern consistent with a role in lung development and our in vitro studies indicated a functional role for TN-C during lung branching morphogenesis.

Duke Scholars

Published In

Dev Biol

DOI

ISSN

0012-1606

Publication Date

February 1994

Volume

161

Issue

2

Start / End Page

615 / 625

Location

United States

Related Subject Headings

  • Tenascin
  • Rats, Sprague-Dawley
  • Rats
  • Pregnancy
  • Morphogenesis
  • Microscopy, Immunoelectron
  • Lung
  • Female
  • Extracellular Matrix Proteins
  • Developmental Biology
 

Citation

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Chicago
ICMJE
MLA
NLM
Young, S. L., Chang, L. Y., & Erickson, H. P. (1994). Tenascin-C in rat lung: distribution, ontogeny and role in branching morphogenesis. Dev Biol, 161(2), 615–625. https://doi.org/10.1006/dbio.1994.1057
Young, S. L., L. Y. Chang, and H. P. Erickson. “Tenascin-C in rat lung: distribution, ontogeny and role in branching morphogenesis.Dev Biol 161, no. 2 (February 1994): 615–25. https://doi.org/10.1006/dbio.1994.1057.
Young SL, Chang LY, Erickson HP. Tenascin-C in rat lung: distribution, ontogeny and role in branching morphogenesis. Dev Biol. 1994 Feb;161(2):615–25.
Young, S. L., et al. “Tenascin-C in rat lung: distribution, ontogeny and role in branching morphogenesis.Dev Biol, vol. 161, no. 2, Feb. 1994, pp. 615–25. Pubmed, doi:10.1006/dbio.1994.1057.
Young SL, Chang LY, Erickson HP. Tenascin-C in rat lung: distribution, ontogeny and role in branching morphogenesis. Dev Biol. 1994 Feb;161(2):615–625.
Journal cover image

Published In

Dev Biol

DOI

ISSN

0012-1606

Publication Date

February 1994

Volume

161

Issue

2

Start / End Page

615 / 625

Location

United States

Related Subject Headings

  • Tenascin
  • Rats, Sprague-Dawley
  • Rats
  • Pregnancy
  • Morphogenesis
  • Microscopy, Immunoelectron
  • Lung
  • Female
  • Extracellular Matrix Proteins
  • Developmental Biology