Abstract

The epidermis is a stratified epithelium, which forms a barrier to maintain the internal milieu in metazoans. Being the outermost tissue, growth of the epidermis has to be strictly coordinated with the growth of the embryo. The key parameters that determine tissue growth are cell number and cell size. So far, it has remained unclear how the size of epidermal cells is maintained and whether it contributes towards epidermal homeostasis. We have used genetic analysis in combination with cellular imaging to show that zebrafish goosepimples/myosin Vb regulates plasma membrane homeostasis and is involved in maintenance of cell size in the periderm, the outermost epidermal layer. The decrease in peridermal cell size in Myosin Vb deficient embryos is compensated by an increase in cell number whereas decrease in cell number results in the expansion of peridermal cells, which requires myosin Vb (myoVb) function. Inhibition of cell proliferation as well as cell size expansion results in increased lethality in larval stages suggesting that this two-way compensatory mechanism is essential for growing larvae. Our analyses unravel the importance of Myosin Vb dependent cell size regulation in epidermal homeostasis and demonstrate that the epidermis has the ability to maintain a dynamic balance between cell size and cell number.

Highlights

  • The epidermis, the outer-most stratified epithelium in metazoans, performs essential functions such as maintenance of body fluids and protection against pathogenic invasion

  • Endocytosis from apical and basolateral domains of peridermal cells contribute to the endosomal pool in the absence of myosin Vb (myoVb) function While we demonstrated that the cytoplasm of gsp/myoVb deficient peridermal cells is filled with endosomal/lysosomal vesicles, their origin remained unclear

  • We show that gsp/myoVb function is essential for the maintenance of peridermal cell size

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Summary

Introduction

The epidermis, the outer-most stratified epithelium in metazoans, performs essential functions such as maintenance of body fluids and protection against pathogenic invasion. The epidermis develops from mono-layered non-neural ectoderm during embryogenesis. It is a bi-layered tissue consisting of the inner basal epidermis and the outer periderm. Tight junctions are an integral part of peridermal cells and contribute to the barrier function [1,4,5]. This early bi-layered epidermis may help in maintaining the interior milieu of the growing vertebrate embryos. The epidermis remains bi-layered during embryonic development in most vertebrates studied. It becomes multilayered before birth in amniotes, including humans, and during metamorphosis in fishes and frog [6,7,8,9,10]

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