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Borday, C.

Publications and source records attributed to Borday, C..

2 recordsLinked to original sources

Regeneration from three cellular sources and ectopic mini-retina formation upon neurotoxic retinal degeneration in Xenopus

Regenerative abilities are not evenly distributed across the animal kingdom. Interestingly, the underlying modalities are also highly variable, even among closely related species. In fish or amphibians, retinal repair can involve the mobilization of different cellular sources, including stem cells of the ciliary marginal zone (CMZ), retinal pigmented epithelial (RPE) cells, or Muller glia. The mechanisms that trigger the recruitment of one cell type over another remain elusive. To investigate whether the magnitude of retinal damage might influence the regeneration modality of the Xenopus retina, we developed a model based on cobalt chloride (CoCl2) intraocular injection, allowing for a dose-dependent control of cell death extent. Analyses in Xenopus laevis revealed that limited CoCl2-mediated neurotoxicity only triggers cone cell loss and results in a few Muller glia cells reentering the cell cycle, without affecting CMZ cell activity or recruiting RPE cells. Conversely, we found that severe CoCl2-induced retinal degeneration not only potentializes the proliferative response of Muller cells, but also enhances CMZ cell proliferation and, unexpectedly triggers an RPE reprogramming event. Although Muller glia could not regenerate cones under these conditions, both CMZ and RPE-derived proliferative cells could. Strikingly, RPE reprogrammed cells self-organized into an ectopic layered mini retina-like structure laid on top of the original retina. It is thus likely that the injury paradigm determines the awakening of different stem-like cell populations exhibiting distinct neurogenic capacities. Besides, we surprisingly found that Xenopus tropicalis also has the ability to recruit Muller cells and reprogram its RPE following CoCl2-induced damage, whereas only CMZ cell proliferation was reported in previously examined degenerative models. Altogether, these findings highlight the critical role of the injury paradigm and reveal that three cellular sources can be reactivated in the very same degenerative model.

developmental biology↗

PFKFB4 control of Akt signaling is essential for premigratory and migratory neural crest formation.

Summary statementPFKFB4 controls neural crest final specification and migration by regulation of AKT signaling or glycolysis.\n\nAbstractNeural crest (NC) specification comprises an early phase, initiating immature NC progenitors formation at neural plate stage, and a later phase at neural fold stage, resulting into functional premigratory NC, able to delaminate and migrate. We found that the NC-GRN triggers up-regulation of pfkfb4 (6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 4) during this late specification phase. As shown in previous studies, PFKFB4 controls AKT signaling in gastrulas and glycolysis rate in adult cells. Here, we focus on PFKFB4 function in NC during and after neurulation, using time-controlled or hypomorph depletions in vivo. We find that PFKFB4 is essential both for specification of functional premigratory NC and for its migration. PFKFB4-depleted embryos fail activating n-cadherin and late NC specifiers, exhibit severe migration defects, resulting in craniofacial defects. AKT signaling mediates PFKFB4 function in NC late specification, while both AKT signaling and glycolysis regulate migration. These findings highlight novel and critical roles of PFKFB4 activity in later stages of NC development, wired into the NC-GRN.

developmental biology↗