Literature DB >> 6968070

Carbohydrate-binding component of amphibian embryo cell surfaces: restriction to surface regions capable of cell adhesion.

M M Roberson, P B Armstrong.   

Abstract

Superficial cells from early amphibian embryos display regional specializations of their cell surfaces. That portion of the plasma membrane facing the perivitelline space (apical surface) is nonadhesive, whereas, in the same cell, the lateral and basal portions of the plasma membrane will adhere to other cells. These adhesive differences are maintained on single cells that have been dissociated from the intact embryo. Extracts of cleavage-stage Rana pipiens embryos are capable of agglutinating formalinized sheep erythrocytes. The hemagglutination activity can be blocked by a yeast mannan and a family of glycoproteins containing high levels of mannose, indicating the presence of a lectin with oligomannosyl specificity. The cell surface location of this carbohydrate-binding component can be demonstrated by the ability of the formalinized sheep erythrocytes to form rosettes with living dissociated embryonic superficial cells. Rosette formation is blocked by the same inhibitors that are effective in blocking the activity of the crude extracts. The formalinized sheep erythrocytes form rosettes only to those cell surface regions of the superficial cells that are capable of adhering to other amphibian embryo cells. Receptors for concanavalin A, a lectin that binds D-mannose and D-glucose residues, have also been shown to be present exclusively over the adhesive regions of the superficial cells. The involvement of a carbohydrate-binding component with oligomannosyl specificity in the adhesive mechanisms of these cells is suggested by this restriction of both the embryonic amphibian lectin and its possible receptors (concanavalin A receptors) to adhesive regions of the cell surface.

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Year:  1980        PMID: 6968070      PMCID: PMC349636          DOI: 10.1073/pnas.77.6.3460

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  15 in total

1.  HEMAGGLUTINATION STUDIES WITH FORMALINIZED ERYTHROCYTES. EFFECT OF BIS-DIAZO-BENZIDINE AND TANNIC ACID TREATMENT ON SENSITIZATION BY SOLUBLE ANTIGEN.

Authors:  W T BUTLER
Journal:  J Immunol       Date:  1963-05       Impact factor: 5.422

2.  Facilitation of pituitary-induced frog ovulation by progesterone in early fall.

Authors:  P A WRIGHT; A R FLATHERS
Journal:  Proc Soc Exp Biol Med       Date:  1961-02

3.  Evidence for receptor-mediated binding of glycoproteins, glycoconjugates, and lysosomal glycosidases by alveolar macrophages.

Authors:  P D Stahl; J S Rodman; M J Miller; P H Schlesinger
Journal:  Proc Natl Acad Sci U S A       Date:  1978-03       Impact factor: 11.205

4.  Regional segregation of ConA receptors on dissociated amphibian embryo cells.

Authors:  M M Roberson; P B Armstrong
Journal:  Exp Cell Res       Date:  1979-08       Impact factor: 3.905

5.  Adherence of Escherichia coli to human mucosal cells mediated by mannose receptors.

Authors:  I Ofek; D Mirelman; N Sharon
Journal:  Nature       Date:  1977-02-17       Impact factor: 49.962

6.  Carbohydrate-binding protein from Polysphondylium pallidum implicated in intercellular adhesion.

Authors:  S D Rosen; D L Simpson; J E Rose; S H Barondes
Journal:  Nature       Date:  1974-11-08       Impact factor: 49.962

7.  Protein-carbonhydrate interaction. 3. Agar gel-diffusion studies on the interaction of Concanavalin A, a lectin isolated from jack bean, with polysaccharides.

Authors:  I J Goldstein; L L So
Journal:  Arch Biochem Biophys       Date:  1965-08       Impact factor: 4.013

8.  Developmentally regulated lectins from chick muscle, brain, and liver have similar chemical and immunological properties.

Authors:  D Kobiler; E C Beyer; S H Barondes
Journal:  Dev Biol       Date:  1978-06       Impact factor: 3.582

9.  Teratocarcinoma stem cells have a cell surface carbohydrate-binding component implicated in cell-cell adhesion.

Authors:  L B Grabel; S D Rosen; G R Martin
Journal:  Cell       Date:  1979-07       Impact factor: 41.582

10.  Trifolin: a Rhizobium recognition protein from white clover.

Authors:  F B Dazzo; W E Yanke; W J Brill
Journal:  Biochim Biophys Acta       Date:  1978-03-20
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  8 in total

Review 1.  On the possible role of endogenous lectins in early animal development.

Authors:  S E Zalik
Journal:  Anat Embryol (Berl)       Date:  1991

2.  Binding of epithelial cells to lectin-coated surfaces.

Authors:  S G Phillips; S L Lui; D M Phillips
Journal:  In Vitro       Date:  1982-08

3.  The masking effect of sialic acid on Con A, PNA and SBA ectoderm binding sites during neurulation in the bantam chick embryo.

Authors:  H Takahashi
Journal:  Anat Embryol (Berl)       Date:  1992

4.  Involvement of a neutral glycolipid in differential cell adhesion in the Xenopus blastula.

Authors:  A P Turner; D Brown; J Heasman; G M Cook; J Evans; L Vickers; C C Wylie
Journal:  EMBO J       Date:  1992-11       Impact factor: 11.598

5.  Ion currents and membrane domains in the cleaving Xenopus egg.

Authors:  D Kline; K R Robinson; R Nuccitelli
Journal:  J Cell Biol       Date:  1983-12       Impact factor: 10.539

Review 6.  Correlation of glycosylation forms with position in amino acid sequence.

Authors:  L Pollack; P H Atkinson
Journal:  J Cell Biol       Date:  1983-08       Impact factor: 10.539

7.  Membrane protein redistribution during Xenopus first cleavage.

Authors:  T J Byers; P B Armstrong
Journal:  J Cell Biol       Date:  1986-06       Impact factor: 10.539

8.  Xenopus laevis lectin is localized at several sites in Xenopus oocytes, eggs, and embryos.

Authors:  M M Roberson; S H Barondes
Journal:  J Cell Biol       Date:  1983-12       Impact factor: 10.539

  8 in total

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