Coupling between dynamic 3D tissue architecture and BMP morphogen signaling during <i>Drosophila</i> wing morphogenesis.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 30760594.
- Also identified by DOI 10.1073/pnas.1815427116 and PMC identifier 6410814.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
At the level of organ formation, tissue morphogenesis drives developmental processes in animals, often involving the rearrangement of two-dimensional (2D) structures into more complex three-dimensional (3D) tissues. These processes can be directed by growth factor signaling pathways. However, little is known about how such morphological changes affect the spatiotemporal distribution of growth factor signaling. Here, using the <i>Drosophila</i> pupal wing, we address how decapentaplegic (Dpp)/bone morphogenetic protein (BMP) signaling and 3D wing morphogenesis are coordinated. Dpp, expressed in the longitudinal veins (LVs) of the pupal wing, initially diffuses laterally within both dorsal and ventral wing epithelia during the inflation stage to regulate cell proliferation. Dpp localization is then refined to the LVs within each epithelial plane, but with active interplanar signaling for vein patterning/differentiation, as the two epithelia appose. Our data further suggest that the 3D architecture of the wing epithelia and the spatial distribution of BMP signaling are tightly coupled, revealing that 3D morphogenesis is an emergent property of the interactions between extracellular signaling and tissue shape changes.
Medical subject headings
- Bone Morphogenetic Proteins
- Drosophila Proteins
- Drosophila melanogaster
- Morphogenesis
- Signal Transduction
- Wings, Animal