Literature DB >> 1370965

Studies on the Thomsen-Friedenreich antigen in human colon with the lectin Amaranthin. Normal and neoplastic epithelium express only cryptic T antigen.

T Sata1, J Roth, C Zuber, B Stamm, S J Rinderle, I J Goldstein, P U Heitz.   

Abstract

The lectin Amaranthin has been shown to be highly specific for the galactose beta 1,3 N-acetylgalactosamine-alpha and sialic acid alpha 2,3 galactose beta 1,3 N-acetylgalactosamine-alpha sequence which represents the Thomsen-Friedenreich (T) antigen and its cryptic form, respectively. Previously, we demonstrated the usefulness of gold-labeled Amaranthin for the histochemical detection of the T antigen and its cryptic form. Application of the galactose oxidase (GO)-Schiff sequence abolished lectin binding to the T antigen but not its cryptic form, and therefore permitted their differentiation. In the present study we have analyzed by light and electron microscopy the distribution and subcellular localization of Amaranthin binding sites in normal, dysplastic and neoplastic colonic epithelium. Furthermore, a monoclonal antibody raised against synthetic galactose bera 1,3 N-acetylgalactosamine-alpha-bovine serum albumin was applied as a reagent for the T antigen. In normal colonic mucosa, two different Amaranthin staining patterns existed: (a) reactivity restricted to the lower portion of the crypts which was principally observed in the left colon, and (b) reactivity along the entire length of the crypts and in the surface epithelium with goblet cell staining in the upper portion of the crypts which was principally observed in the right colon. This Amaranthin staining was resistant to GO-Schiff treatment. No immunostaining with the monoclonal anti-T antigen was observed. Investigation of transitional mucosa, adenocarcinomas of different degrees of differentiation and mucinous carcinomas as well as adenomas with different degrees of dysplasia all revealed positive Amaranthin staining. The lectin staining was resistant to GO-Schiff treatment, and immunolabeling with the monoclonal antibody against the T antigen was absent. These results indicate that only the cryptic form of the T antigen is expressed in normal, dysplastic and neoplastic human colonic epithelium.

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Year:  1992        PMID: 1370965

Source DB:  PubMed          Journal:  Lab Invest        ISSN: 0023-6837            Impact factor:   5.662


  6 in total

Review 1.  Protein glycosylation in the endoplasmic reticulum and the Golgi apparatus and cell type-specificity of cell surface glycoconjugate expression: analysis by the protein A-gold and lectin-gold techniques.

Authors:  J Roth
Journal:  Histochem Cell Biol       Date:  1996-07       Impact factor: 4.304

Review 2.  Applications of immunogold and lectin-gold labeling in tumor research and diagnosis.

Authors:  J Roth; C Zuber; P Komminoth; T Sata; W P Li; P U Heitz
Journal:  Histochem Cell Biol       Date:  1996-07       Impact factor: 4.304

Review 3.  Lectins for histochemical demonstration of glycans.

Authors:  Jürgen Roth
Journal:  Histochem Cell Biol       Date:  2011-07-31       Impact factor: 4.304

4.  Thomsen-Friedenreich-related carbohydrate antigens in normal adult human tissues: a systematic and comparative study.

Authors:  Y Cao; P Stosiek; G F Springer; U Karsten
Journal:  Histochem Cell Biol       Date:  1996-08       Impact factor: 4.304

Review 5.  Cellular sialoglycoconjugates: a histochemical perspective.

Authors:  J Roth
Journal:  Histochem J       Date:  1993-10

6.  Colonic carcinogenesis along different genetic routes: glycophenotyping of tumor cases separated by microsatellite instability/stability.

Authors:  Johannes Gebert; Matthias Kloor; Jennifer Lee; Michaela Lohr; Sabine André; Rudolf Wagner; Juergen Kopitz; Hans-Joachim Gabius
Journal:  Histochem Cell Biol       Date:  2012-05-08       Impact factor: 4.304

  6 in total

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