Literature DB >> 6548456

Developmentally regulated plasmalemmal glycoconjugates of the surface and neural ectoderm.

J R Currie, M F Maylié-Pfenninger, K H Pfenninger.   

Abstract

The plasmalemmal glycoconjugates of the ectoderm surrounding the rat embryo's caudal neuropore were mapped at the ultrastructural level, using various lectin probes. These included the agglutinins of wheat germ, soybean, Ricinus communis, Lotus tetragonolobus, and Canavalia ensiformis. Each lectin produced a characteristic binding pattern. Comparison of precursor cells of surface ectoderm, neural crest, and neural tube revealed that, even prior to neural tube formation, these three cell types can be distinguished by the sets of lectin receptors they express on their apical plasmalemma. The high density of lectin receptors found at the open neural groove level decreases dramatically during neurulation. Further changes in surface glycoconjugates must occur during neuronal differentiation because sprouting neurons exhibit yet another lectin binding pattern (K.H. Pfenninger, M.-F. Maylié-Pfenninger, L. B. Friedman, and P. Simkowitz, 1984, Dev. Biol. 106, 97-108). These results indicate that the commitment of ectodermal cells to diverging lineages (epidermis, neural crest, and tube) is reflected in their surface carbohydrates and occurs while they are still part of a continuous epithelial sheet. Furthermore, the plasmalemmal glycoconjugates of the ectoderm are developmentally regulated, and particularly dramatic changes in glycoconjugates expression are linked to neurulation.

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Year:  1984        PMID: 6548456     DOI: 10.1016/0012-1606(84)90067-8

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  11 in total

1.  Transient appearance of and regional differences in apical cell surface materials during early morphogenesis of the chicken lens.

Authors:  E H Webster; M E Uknis
Journal:  Histochem J       Date:  1987-04

2.  Ultrastructural localization of WGA, RCA I, LFA and SBA binding sites in the seven-day-old mouse embryo.

Authors:  R Herken; B Sander; M Hofmann
Journal:  Histochemistry       Date:  1990

3.  The incorporation and dispersion of cells and latex beads on microinjection into the amniotic cavity of the mouse embryo at the early-somite stage.

Authors:  W Y Chan; K K Lee
Journal:  Anat Embryol (Berl)       Date:  1992

4.  Cell surface proteins of wholeXenopus embryos identified by radioiodination.

Authors:  Judith Litvin; Mary Lou King
Journal:  Rouxs Arch Dev Biol       Date:  1989-10

5.  Lectin-binding patterns in the embryonic human paraxial mesenchyme.

Authors:  W Götz; D Frisch; R Osmers; R Herken
Journal:  Anat Embryol (Berl)       Date:  1993-12

6.  The distribution of cell surface glycoconjugates during mouse secondary neurulation.

Authors:  C M Griffith; M J Wiley
Journal:  Anat Embryol (Berl)       Date:  1989

7.  Binding pattern of ferritin-labeled lectins (RCAI and WGA) during neural tube closure in the bantam embryo.

Authors:  H Takahashi; R I Howes
Journal:  Anat Embryol (Berl)       Date:  1986

8.  Patterns of lectin binding during mammalian neurogenesis.

Authors:  D B Wilson; D P Wyatt
Journal:  J Anat       Date:  1995-02       Impact factor: 2.610

9.  The cell surface coat in neurulating mouse and rat embryos, studied with lectins.

Authors:  A E Smits-van Prooije; R E Poelmann; A F Gesink; M J van Groeningen; C Vermeij-Keers
Journal:  Anat Embryol (Berl)       Date:  1986

10.  Changes in peanut lectin binding sites on the neuroectoderm during neural tube formation in the bantam chick embryo.

Authors:  H Takahashi
Journal:  Anat Embryol (Berl)       Date:  1988
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