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Brunt, L.

Publications and source records attributed to Brunt, L..

3 recordsLinked to original sources

Rab8a-positive vesicles transport Wnt8a along cytonemes in zebrafish embryogenesis.

Wnt signalling is a conserved pathway that orchestrates key developmental processes by regulating cell fate, proliferation, and tissue organisation. While the production and secretion of Wnt ligands are well characterised, less is known about how lipid-modified Wnts are delivered for long-range communication. Recently, cytonemes - actin-based signalling filopodia - have been identified as transporters of Wnts over distances to target specific cells in embryogenesis. Here, we characterise Rab8a-dependent vesicular trafficking as a crucial step in this process. Using human cell lines and zebrafish embryos, we show that Wnt ligands, such as Wnt8a, are transported with their carrier protein Wntless (Wls) in Rab8a-positive vesicles along cytonemes, where they fuse at the tips to enable hand-over and signal activation in neighbouring cells. Disruption of Rab8a function results in the intracellular retention of Wnt8a, reduces Wnt spreading and paracrine signalling, and alters embryonic patterning, consistent with reduced Wnt/{beta}-catenin function. Conversely, Rab8a activation enhances Wnt8a dissemination, leading to increased long-range signalling and, consequently, patterning defects in embryogenesis. Our findings uncover a dedicated intracellular trafficking route for Wnt delivery to and along cytonemes, offering new insights into how the spatial precision of Wnt spreading in vertebrate tissues is achieved.

developmental biology↗

Cytoneme-mediated transport of active Wnt5b/Ror2 complexes in zebrafish gastrulation

Chemical signaling is the primary means by which cells communicate in the embryo. The underlying principle refers to a group of ligand-producing cells and a group of cells that respond to this signal because they express the appropriate receptors. In the zebrafish embryo, Wnt5b binds to the receptor Ror2 to trigger the Wnt/Planar Cell Polarity (Wnt/PCP) signaling pathway to regulate tissue polarity and cell migration. However, it is still unclear how this lipophilic ligand is transported from the source cells through the aqueous extracellular space to the target tissue. Here we show that Wnt5b, together with Ror2, is loaded on long protrusions. The active Wnt5b/Ror2 complexes are handed over from these cytonemes to the receiving cell to trigger Wnt/PCP signaling, regardless of whether the cell expresses functional receptors. On the tissue level, we show that cytoneme-dependent spreading of active Wnt5b/Ror2 affects convergence and extension in the zebrafish gastrula.

developmental biology↗

Vangl2 regulates the dynamics of Wnt cytonemes in vertebrates

The Wnt signalling network regulates cell proliferation and cell differentiation as well as migration and polarity in development of multicellular organisms. However, it is still unclear how distribution of Wnt ligands is precisely controlled to fulfil all of these different functions. Here, we show that the four-pass transmembrane protein Vangl2 occupies a central role in determining the distribution of Wnt by cytonemes in vertebrate tissue. In zebrafish epiblast cells, mouse intestinal telocytes and human gastric cancer cells, activation of Vangl2 leads to the generation of fewer but extremely long cytonemes, which start to branch and deliver Wnt protein to multiple cells. The Vangl2-activated cytonemes increase Wnt/{beta}-catenin signalling in the surrounding cells. Concordantly, inhibition of Vangl2 function leads to the formation of shorter cytonemes and reduced paracrine Wnt/{beta}-catenin signal activation. A mathematical model simulating the observed Vangl2 functions on cytonemes in zebrafish gastrulation predicts an anterior shift of the morphogenetic signalling gradient, altered tissue patterning, and a loss of the sharpness of tissue domains. We confirmed these predictions during anteroposterior patterning in the zebrafish neural plate. In summary, we show that Vangl2 - a core member of the PCP signalling component - is fundamental to paracrine Wnt/{beta}-catenin signalling by controlling cytoneme behaviour in vertebrate development and tissue homeostasis.

developmental biology↗