Down-regulation of human sialyltransferase gene expression during in vitro human keratinocyte cell line differentiation

Akiyoshi Taniguchi, Kojiro Matsumoto

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30 Citations (Scopus)

Abstract

Sialic acids play important roles in biological processes, such as cell-cell communication and cell-matrix interaction. Histochemical analysis using PNA and LFA lectin has shown that the expression of α2,3-sialic acid linked to Galβ1,3GalNAc is high in basal cells and decreases following further keratinocyte differentiation. In the present study, we used an in vitro keratinocyte cell line differentiation model to study expression of α2,3-sialic acid linked to Gal β1,3 GalNAc. Treatment of the human papillomavirus type 16-immortalized human keratinocyte (PHK16) cell line with high concentrations (1.0 mM) of Ca2+ resulted in PHK16 cell differentiation and redistribution of PNA binding glycoproteins. The synthesis of α2,3-sialic acid linked to Galβ1,3GalNAc is mediated by three β-galactoside α2,3-sialytransferases, which are the gene products of hST3O, hST3O/N and hST3 Gal II. Ca2+ treatment of PHK16 cells decreased the mRNA expression of hST3O/N, whereas the mRNA of hST3O and hST3Gal II was not detected by Northern blot analysis, suggesting that the hST3O/N gene is responsible for sialic acid down regulation during keratinocyte differentiation. In order to examine transcriptional regulation of the hST3O/N gene, we first determined the transcriptional starting sites of the hST3O/N gene in PHK 16 using 5'-RACE analysis. Two kinds of type B isoforms, types B3 and BX, were identified. Type BX is a novel isoform related to the type B form, but which differs upstream of the B3 exon. The results of Northern blot analysis using a type BX-specific probe suggest that the B3 promoter may be regulated by Ca2+. Using a luciferase assay, we identified a functional DNA portion within hST3O/N genomic DNA that confers negative transcriptional regulation on the hST3O/N B3 promoter during Ca2+ stimulated human keratinocyte differentiation. This element contains some putative transcriptional factor binding sequence motifs such as AP2.

Original languageEnglish
Pages (from-to)177-183
Number of pages7
JournalBiochemical and Biophysical Research Communications
Volume243
Issue number1
DOIs
Publication statusPublished - 1998 Feb 4
Externally publishedYes

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Sialyltransferases
Keratinocytes
Gene expression
N-Acetylneuraminic Acid
Cell Differentiation
Down-Regulation
Cells
Gene Expression
Cell Line
Genes
Cell Communication
Northern Blotting
Protein Isoforms
Sialic Acids
Biological Phenomena
Galactosides
Messenger RNA
Human papillomavirus 16
DNA
Luciferases

ASJC Scopus subject areas

  • Biochemistry
  • Biophysics
  • Molecular Biology

Cite this

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title = "Down-regulation of human sialyltransferase gene expression during in vitro human keratinocyte cell line differentiation",
abstract = "Sialic acids play important roles in biological processes, such as cell-cell communication and cell-matrix interaction. Histochemical analysis using PNA and LFA lectin has shown that the expression of α2,3-sialic acid linked to Galβ1,3GalNAc is high in basal cells and decreases following further keratinocyte differentiation. In the present study, we used an in vitro keratinocyte cell line differentiation model to study expression of α2,3-sialic acid linked to Gal β1,3 GalNAc. Treatment of the human papillomavirus type 16-immortalized human keratinocyte (PHK16) cell line with high concentrations (1.0 mM) of Ca2+ resulted in PHK16 cell differentiation and redistribution of PNA binding glycoproteins. The synthesis of α2,3-sialic acid linked to Galβ1,3GalNAc is mediated by three β-galactoside α2,3-sialytransferases, which are the gene products of hST3O, hST3O/N and hST3 Gal II. Ca2+ treatment of PHK16 cells decreased the mRNA expression of hST3O/N, whereas the mRNA of hST3O and hST3Gal II was not detected by Northern blot analysis, suggesting that the hST3O/N gene is responsible for sialic acid down regulation during keratinocyte differentiation. In order to examine transcriptional regulation of the hST3O/N gene, we first determined the transcriptional starting sites of the hST3O/N gene in PHK 16 using 5'-RACE analysis. Two kinds of type B isoforms, types B3 and BX, were identified. Type BX is a novel isoform related to the type B form, but which differs upstream of the B3 exon. The results of Northern blot analysis using a type BX-specific probe suggest that the B3 promoter may be regulated by Ca2+. Using a luciferase assay, we identified a functional DNA portion within hST3O/N genomic DNA that confers negative transcriptional regulation on the hST3O/N B3 promoter during Ca2+ stimulated human keratinocyte differentiation. This element contains some putative transcriptional factor binding sequence motifs such as AP2.",
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