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First published online 27 July 2004
doi: 10.1242/dev.01285
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Divisions of Developmental Biology and Ophthalmology, Children's Hospital Research Foundation, 3333 Burnet Avenue, Cincinnati, OH 45229, USA
¶ Author for correspondence (e-mail: richard.lang{at}chmcc.org)
Accepted 3 June 2004
The lacrimal gland provides an excellent model with which to study the
epithelial-mesenchymal interactions that are crucial to the process of
branching morphogenesis. In the current study, we show that bone morphogenetic
protein 7 (Bmp7) is expressed with a complex pattern in the developing gland
and has an important role in regulating branching. In loss-of-function
analyses, we find that Bmp7-null mice have distinctive reductions in
lacrimal gland branch number, and that inhibition of Bmp activity in gland
explant cultures has a very similar consequence. Consistent with this,
exposure of whole-gland explants to recombinant Bmp7 results in increased
branch number. In determining which cells of the gland respond directly to
Bmp7, we have tested isolated mesenchyme and epithelium. We find that, as
expected, Bmp4 can suppress bud extension in isolated epithelium stimulated by
Fgf10, but interestingly, Bmp7 has no discernible effect. Bmp7 does, however,
stimulate a distinct response in mesenchymal cells. This manifests as a
promotion of cell division and formation of aggregates, and upregulation of
cadherin adhesion molecules, the junctional protein connexin 43 and of
-smooth muscle actin. These data suggest that in this branching system,
mesenchyme is the primary target of Bmp7 and that formation of mesenchymal
condensations characteristic of signaling centers may be enhanced by Bmp7.
Based on the activity of Bmp7 in promoting branching, we also propose a model
suggesting that a discrete region of Bmp7-expressing head mesenchyme may be
crucial in determining the location of the exorbital lobe of the gland.
Key words: Bone morphogenetic protein, Bmp, Branching morphogenesis, Lacrimal gland
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