Abstract
Intercalation allows cells to exchange positions in a spatially oriented manner in an array of diverse processes, spanning convergent extension in embryonic gastrulation to the formation of tubular organs. However, given the co-occurrence of cell intercalation and changes in cell shape, it is sometimes difficult to ascertain their respective contribution to morphogenesis. A well-established model to analyse intercalation, particularly in tubular organs, is the Drosophila tracheal system. There, fibroblast growth factor (FGF) signalling at the tip of the dorsal branches generates a ‘pulling’ force believed to promote cell elongation and cell intercalation, which account for the final branch extension. Here, we used a variety of experimental conditions to study the contribution of cell elongation and cell intercalation to morphogenesis and analysed their mutual requirements. We provide evidence that cell intercalation does not require cell elongation and vice versa. We also show that the two cell behaviours are controlled by independent but simultaneous mechanisms, and that cell elongation is sufficient to account for full extension of the dorsal branch, while cell intercalation has a specific role in setting the diameter of this structure. Thus, rather than viewing changes in cell shape and cell intercalation as just redundant events that add robustness to a given morphogenetic process, we find that they can also act by contributing to different features of tissue architecture.
Highlights
Cell intercalation is a key mechanism underlying tissue remodelling during morphogenesis
We show that the two cell behaviours are controlled by independent but simultaneous mechanisms, and that cell elongation is sufficient to account for full extension of the dorsal branch, while cell intercalation has a specific role in setting the diameter of this structure
Cell intercalation is not required for full dorsal branch extension
Summary
Cell intercalation is a key mechanism underlying tissue remodelling during morphogenesis. Activation of the fibroblast growth factor (FGF) receptor Breathless (Btl) at the tip of the tracheal branches by its ligand Branchless (Bnl), which is secreted by nearby cells, induces an attraction of the tracheal cells towards neighbouring cells [13] This attraction generates a ‘pulling’ force believed to promote a change in cell shape (cell elongation) and to drive the rearrangement of cells from a sideby-side to an end-to-end arrangement (cell intercalation), a process accompanied by the conversion of intercellular to autocellular adherens junctions (AJs) [9,11]. Rather than viewing changes in cell shape and cell intercalation as just redundant events that add robustness to a given morphogenetic process, we find that they can act by contributing to different features of tissue architecture
Published Version (Free)
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have