Cytoskeleton gradients in three dimensions during neurulation in the rabbit

Abstract

Morphogenetic movements leading to the formation of the neural tube and cellular differentiation leading to neuronal and glial cell lineages are both part of early development of the vertebrate nervous system. In order to analyze the degree of overlap between these processes, cellular differentiation during the shaping of the neural plate is investigated immunohistochemically by using monoclonal intermediate filament protein antibodies and the 7.5–8.0‐day‐old rabbit embryo as a model. Western blotting is used to confirm the specificity of the antibodies, which include a new monoclonal vimentin antibody suitable for double‐labeling in combination with monoclonal cytokeratin (and fibronectin) antibodies. Starting in the early somite embryo and concomitant with neural plate folding, a gradual loss of cytokeratin 8 (and 18) expression in the neuroepithelium is mirrored by a gain in virnentin expression with partial coexpression of both proteins. At the prospective rhombencephalic and spinocaudal levels, vimentin expression, in particular, changes (i. e., increases) along gradients in three dimensions: along the longitudinal axis of each neuroepithelial cell from bssal to apical, in the transverse plane of the embryo from dorsolateral to veritromedial and along the craniocaudal axis from prospective rhombencephalic toward spinocaudal levels of the neural plate. At the prospective mes‐ and prosencephalic levels, the expression change also proceeds from basal to apical within each neuroepithelial cell, but along the other axes described here, the progress in expression change is more complex. Although the functional meaning of these highly ordered expression changes is at present unclear, the gradients suggest a novel pattern of neuroepithelial differentiation which may be functionally related to the process of interkinetic nuclear migration (Sauer [1935] J. Comp. Neurol. 62:377–402) and which partially coincides with the morphogenetic movements involved in the shaping of the neural plate.