Florencia Cavodeassi and Steve Wilson
Original paper reference:
Early stages of zebrafish eye formation require the coordinated activity of Wnt11, Fz5 and the Wnt/β-catenin pathway
You might not realise it but your eyes are in fact part of your brain. Early in embryonic development, the eyes arise as outgrowths from the forming brain. How does a subset of brain cells become destined to form the eyes and how do these cells then undergo the complex movements that must occur during eye formation? In this study, we addressed the role of genes functioning in the Wnt pathway, a cell-to-cell signalling pathway, in the regulation of early steps of eye formation.
The primordium of the mature eyes is specified as a single "eye-field" of cells at very early stages of embryonic development. At this stage, the nervous system is just a simple sheet of cells called the neural plate. As the neural plate folds up to form the brain, the eye-field splits in two and evaginates from the brain to form left and right eyes.
In zebrafish embryos, the eye field and other regions of the prospective brain can be readily visualised within the neural plate by the overlapping expression of various genes encoding transcription factors. The eye field is surrounded anteriorly by the prospective telencephalon, and posteriorly by the prospective diencephalon (Figure 1).
Figure 1: (A) Organisation of brain territories at neural plate stage. The groups of cells giving rise to each territory are shown in different colors. (B-D) The same colour code is used to show the relative positions of the different territories in embryonic brains at a later stage of development, from lateral (B), dorsal (C) and ventral (D) views. Modified from Cavodeassi et al., (2009) Squire LR (ed.) Encyclopedia of Neuroscience, vol. 4, 321-325
The Wnt signalling pathway has been well studied and work done by our group and others, suggested a model whereby a gradient of Wnt activity specifies different regional fates within the anterior neural plate. The model suggested high levels of Wnt activity specify diencephalic fates and lower levels of Wnts specify gradually more anterior fates, such as the eye field and the telencephalon. In this study, we re-examined the role of the Wnt pathway during eye field specification, and found that it is more complex than expected. Wnt proteins can activate several different signalling cascades: simplistically, Wnt/β-catenin signalling leads to changes in gene expression and the identity of cells (like brain versus eye) whereas Wnt/PCP signalling leads to changes in cell shape and movements.
By doing a series of experiments where we activated or switched off the Wnt pathway locally within the anterior neural plate, we found that these two branches of the pathway have very different effects on eye formation (Figure 2). High levels of Wnt/β-catenin signalling tells cells to become diencephalic brain and blocks eye formation. In contrast, Wnt/PCP activity within the eye field promotes eye formation, and it does so, at least partially, by antagonising the Wnt/β-catenin pathway. Each branch of the Wnt pathway appears to be activated by a different combination of Wnts and their receptors (called Fzs) in the nascent forebrain. Thus, Wnt8b and Fz8a activate the Wnt/β-catenin pathway, while Wnt11 and Fz5 activate the non-canonical pathway.
Figure 2: Manipulation of two branches of the Wnt pathway has opposite effects on eye formation. Dorsal views of embryos with transplants of cells (labelled in brown) activating different branches of the Wnt pathway. Wnt8b/βcatenin activity blocks eye formation (asterisk in B), while Wnt11/PCP activity leads to the formation of bigger, misshapen eyes (asterisk in C). A control transplant expressing GFP does not have any effect on eye development (A). The optic vesicles are labelled by the expression of the rx2 gene (blue). Anterior is to the left.