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L H Barton

Publications and source records attributed to L H Barton.

3 recordsLinked to original sources

Secondary palatal development in the New Zealand white rabbit: a scanning electron microscopic study.

Examination of surface topography in prefusion stages of secondary palatal development in rabbit embryos reveals a sequence of alterations in the surface cells of the epithelium along the medial margins of the palatal processes. A progressive increase in cellular protrusions resembling lamellipodia and filopodia, as well as cellular necrosis, is observed in those areas that undergo fusion. The changes precede fusion and are restricted to fusion sites. Prior to and at the time of epithelial contact between palatal processes, many long slender cellular protrusions are seen bridging the gap between the approximating tissues. The localization of the epithelial alterations and the appearance of similar cellular morphology in other embryonic epithelial fusion events strongly suggest: either an active role of the epithelial cells in the fusion of the secondary palate, or some common fundamental biochemical events that may facilitate or are responsible for the initial adhesion of such tissues.

Animals↗

Distribution of glycogen in prefusion human palatal epithelium.

Various stages of embryonic human secondary palatal development were examined for the presence of epithelial glycogen. Utilizing periodic acid-Schiff's reagent staining of thick plastic sections and osmium ferrocyanide enhancement of thin sections, dramatic changes in epithelial glycogen distribution were noted during palatogenesis. Prior to fusion, the epithelium destined to adhere in the midline exhibited a marked diminution of glycogen in the superficial cell layer. This cell layer was composed of slender dense cells and cuboidal cells undergoing lysis. Adjacent nonfusing epithelium was markedly different and contained large glycogen reserves in its superficial cell layer. Glycogen may play a role either as precursor for specific adhesive macromolecules or as a physical agent capable under the influence of appropriate enzymes of causing cell lysis.

Cell Adhesion↗

Extracellular coat in developing human palatal processes: electron microscopy and ruthenium red binding.

The prefusion epithelium of human palatal processes was examined for evidence of specialization which might facilitate epithelial adherence with the opposing palatal process. A surface coat stained with ruthenium red (RR) was found on all apical aspects of the palatal epithelium. In the prefusion regions, RR staining was also observed in the spaces between the superficial cells of the epithelium and in necrotic cells. Adjacent oral and nasal epithelium excluded the RR below the level of the apical junctional complex. In the absence of RR, a dense material was observed in the most superficial intercellular spaces of the prefusion region. Many superficial cells in the area were in various stages of necrosis. The combination of degenerating surface cells and an accumulation of a poly-anionic substance such as glycoprotein may facilitate epithelial adherence between opposing human palatal processes.

Cell Adhesion↗