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Am J Physiol Lung Cell Mol Physiol 286: L1179-L1187, 2004; doi:10.1152/ajplung.00188.2003
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Matrix GLA protein modulates branching morphogenesis in fetal rat lung

Kirk A. Gilbert and Stephen R. Rannels

Department of Cellular and Molecular Physiology, The Pennsylvania State University College of Medicine, Hershey, Pennsylvania 17033

Submitted 10 December 2003 ; accepted in final form 7 January 2004

The regulation of matrix {gamma}-carboxyglutamic acid protein (MGP) expression during the process of lung branching morphogenesis and development was investigated. MGP mRNA expression was determined over an embryonic and postnatal time course and shown to be developmentally regulated. Immunohistochemical analysis revealed increased staining for MGP in peripheral mesenchyme surrounding distal epithelial tubules. Fetal lung explants were used as an in vitro growth model to examine expression and regulation of MGP during branching morphogenesis. MGP mRNA expression over the culture interval mimicked the in vivo time course. Explants cultured in the presence of antibodies against MGP showed gross dilation and reduced terminal lung bud counts, accompanied by changes in MGP, sonic hedgehog, and patched mRNA expression. Similarly, antifibronectin antibody treatment resulted in explant dilation and reduced MGP expression, providing evidence for an interaction with MGP and fibronectin. Conversely, intraluminal microinjection of anti-MGP antibodies had no effect either on explant growth or MGP expression, supporting the hypothesis that MGP exerts its effects through the mesenchyme. Taken together, the results suggest that MGP plays a role in lung growth and development, likely via temporally and spatially specific interactions with other branching morphogenesis-related proteins to influence growth processes.

lung development; vitamin K; sonic hedgehog; patched; bone morphogenetic protein-4; fibroblast growth factor-10; fibronectin; explants; mesenchyme; {gamma}-carboxyglutamic acid


Address for reprint requests and other correspondence: S. R. Rannels, Dept. of Cellular and Molecular Physiology, H-166, The Pennsylvania State Univ. College of Medicine, 500 Univ. Drive, Hershey, PA 17033 (E-mail: srannels{at}psu.edu).




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