Abstract

BackgroundIn the spider Cupiennius salei about 30 groups of neural precursors are generated per hemi-segment during early neurogenesis. Analysis of the ventral neuromeres after invagination of the primary neural precursor groups revealed that secondary neural precursors arise during late embryogenesis that partially do not differentiate until larval stages.ResultsIn contrast to the primary groups, the secondary invaginating cells do not detach from each other after invagination but maintain their epithelial character and form so-called epithelial vesicles. As revealed by dye labeling, secondary neural precursors within epithelial vesicles do not show any morphological features of differentiation indicating that the formation of epithelial vesicles after invagination leads to a delay in the differentiation of the corresponding neural precursors. About half of the secondary neural precursor groups do not dissociate from each other during embryogenesis indicating that they provide neural precursors for larval and adult stages.ConclusionsSecondary neural precursors are arrested in an immature state by formation of epithelial vesicles. This mechanism facilitates the production of larval neural precursors during embryogenesis. I discuss the evolutionary changes that have occured during neural precursor formation in the arthropod group and present a model for the basal mode of neurogenesis.

Highlights

  • In the spider Cupiennius salei about 30 groups of neural precursors are generated per hemi-segment during early neurogenesis

  • I discuss the evolutionary changes that have occured during neural precursor formation in the arthropod group and present a model for the basal mode of neurogenesis

  • Formation of epithelial vesicles – a conserved character in arthropod neurogenesis? Analysis of the ventral neuromeres of spider embryos after invagination of the primary neural precursor groups revealed that secondary neural precursors arise during late embryogenesis that partially do not differentiate until larval stages

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Summary

Introduction

In the spider Cupiennius salei about 30 groups of neural precursors are generated per hemi-segment during early neurogenesis. Groups of neural precursors invaginate from the ventral neuroectoderm in a regular, strikingly similar pattern in spiders (chelicerates) and myriapods, while in insects and crustaceans single neural precursors are selected. This modification may be the basis for variations in the functions of spider and myriapod neurons, since a comparison of early segmentally repeated neurons that pioneer the major axon tracts in crustaceans and insects has not revealed any similarities in cell body positions or axonal outgrowths to myriapod neurons [6,7]

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