Histochemistry and Cell Biology

, Volume 110, Issue 3, pp 273–284

Expression of smooth muscle markers in the developing murine lung: potential contractile properties and lineal descent

Authors

  • K. Jostarndt-Fögen
    • Anatomisches Institut, Universität Bern, Bühlstrasse 26, CH-3012 Bern, Switzerland Tel. +41-31-631 4625; fax +41-31-631 3807 e-mail draeger@ana.unibe.ch
  • Valentin Djonov
    • Anatomisches Institut, Universität Bern, Bühlstrasse 26, CH-3012 Bern, Switzerland Tel. +41-31-631 4625; fax +41-31-631 3807 e-mail draeger@ana.unibe.ch
  • A. Draeger
    • Anatomisches Institut, Universität Bern, Bühlstrasse 26, CH-3012 Bern, Switzerland Tel. +41-31-631 4625; fax +41-31-631 3807 e-mail draeger@ana.unibe.ch
ORIGINAL PAPER

DOI: 10.1007/s004180050289

Cite this article as:
Jostarndt-Fögen, K., Djonov, V. & Draeger, A. Histochemistry (1998) 110: 273. doi:10.1007/s004180050289

Abstract

 Contractile cells in the mammalian lung develop in close association with the outgrowing stem bronchi. Fully differentiated smooth muscle cells are typically found in proximal regions, residing in the substantial muscular walls of the major airways and blood vessels. More distally, cells expressing markers of differentiated smooth muscle cells to a variable degree, and which may therefore possess contractile properties, are to be found scattered around the interstitium. We have investigated the temporal and spatial distribution of smooth muscle lineage markers (smooth muscle myosin mRNA) and of those indicative of contractile function (metavinculin mRNA) in the murine lung. In the smooth muscle layers of the bronchi and major blood vessels, these genes are expressed from the onset of pulmonary budding, concurrently with the appearance of α-smooth muscle actin and calponin proteins. During fetal development, smooth muscle-associated genes and proteins are restricted to this committed smooth muscle population. The first signs of myofibroblast or pericyte differentiation become manifest perinatally, when their expression of α-smooth muscle actin escalates. In the adult lung, such cells may be readily pin-pointed by their positive reaction for metavinculin mRNA, but, at maturity, they do not always coexpress α-smooth muscle actin.

Copyright information

© Springer-Verlag Berlin Heidelberg 1998