Abstract

Background: E-cadherin is the major adhesion receptor in epithelial adherens junctions (AJs). On established epidermis, E-cadherin performs fine-tuned cell-cell contact remodeling to maintain tissue integrity, which is characterized by modulation of cell shape, size and packing density. In zebrafish, the organization and distribution of E-cadherin in AJs during embryonic epidermis development remain scarcely described. Methods: Combining classical immunofluorescence, deconvolution microscopy and 3D-segmentation of AJs in epithelial cells, a quantitative approach was implemented to assess the spatial and temporal distribution of E-cadherin across zebrafish epidermis between 24 and 72 hpf. Results: increasing levels of E-cadh protein parallel higher cell density and the appearance of hexagonal cells in the enveloping layer (EVL) as well as the establishments of new cell-cell contacts in the epidermal basal layer (EBL), being significantly between 31 and 48 hpf . Conclusions: Increasing levels of E-cadherin in AJs correlates with extensive changes in cell morphology towards hexagonal packing during the epidermis morphogenesis.

Highlights

  • The skin is the largest organ of the body in direct contact with the environment

  • E-cadh was observed in adherens junctions (AJs) in enveloping layer (EVL) cells and weakly detected in epidermal basal layer (EBL) cells (Figure 1b–c)

  • To elucidate whether the increase could be due to the appearance of more cell-cell contacts per EVL area, cell density was estimated globally and for hexagonal cells, and expressed as cell packing indexes (Figure 4a, b). These results showed a significant increment in cell density in the EVL that was characterized by the establishment of hexagonal cell morphology from 24 to 72 hpf

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Summary

Introduction

The skin is the largest organ of the body in direct contact with the environment. It has a complex structure, being constituted by many different tissues. E-cadherin performs fine-tuned cell-cell contact remodeling to maintain tissue integrity, which is characterized by modulation of cell shape, size and packing density. Methods: Combining classical immunofluorescence, deconvolution microscopy and 3D-segmentation of AJs in epithelial cells, a quantitative approach was implemented to assess the spatial and temporal distribution of E-cadherin across zebrafish epidermis between 24 and 72 hpf. Conclusions: Increasing levels of E-cadherin in AJs correlates with extensive changes in cell morphology towards hexagonal packing during the epidermis morphogenesis

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