Fluoride affects enamel protein content via TGF-β1-mediated KLK4 inhibition

M Suzuki, M Shin, J P Simmer, J D Bartlett

Research output: Contribution to journalArticle

25 Citations (Scopus)

Abstract

Dental fluorosis is caused by chronic high-level fluoride (F(-)) exposure during enamel development, and fluorosed enamel has a higher than normal protein content. Matrix metalloproteinase 20 cleaves enamel matrix proteins during the secretory stage, and KLK4 further cleaves these proteins during the maturation stage so that the proteins can be reabsorbed from the hardening enamel. We show that transforming growth factor β1 (TGF-β1) can induce Klk4 expression, and we examine the effect of F(-) on TGF-β1 and KLK4 expression. We found that in vivo F(-) inhibits Klk4 but not Mmp20 transcript levels. LacZ-C57BL/6-Klk4 (+/LacZ) mice have LacZ inserted in frame at the Klk4 translation initiation site so that the endogenous Klk4 promoter drives LacZ expression in the same temporal/spatial way as it does for Klk4. KLK4 protein levels in rat enamel and β-galactosidase staining in LacZ-C57BL/6-Klk4 (+/LacZ) mouse enamel were both significantly reduced by F(-) treatment. Since TGF-β1 induces KLK4 expression, we tested and found that F(-) significantly reduced Tgf-β1 transcript levels in rat enamel organ. These data suggest that F(-)-mediated downregulation of TGF-β1 expression contributes to reduced KLK4 protein levels in fluorosed enamel and provides an explanation for why fluorosed enamel has a higher than normal protein content.

Original languageEnglish (US)
Pages (from-to)1022-7
Number of pages6
JournalJournal of Dental Research
Volume93
Issue number10
DOIs
StatePublished - Oct 2014
Externally publishedYes

Fingerprint

Transforming Growth Factors
Dental Enamel
Fluorides
Proteins
Matrix Metalloproteinase 20
Enamel Organ
Galactosidases
Dental Fluorosis
Down-Regulation
Staining and Labeling

Keywords

  • Ameloblasts/drug effects
  • Amelogenin/analysis
  • Animals
  • Cariostatic Agents/pharmacology
  • Cell Line, Tumor
  • Cells, Cultured
  • Dental Enamel Proteins/drug effects
  • Down-Regulation
  • Enamel Organ/drug effects
  • Fluorides/pharmacology
  • Gene Knock-In Techniques
  • Kallikreins/analysis
  • Lac Operon/drug effects
  • Matrix Metalloproteinase 20/drug effects
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred Strains
  • Rats
  • Rats, Sprague-Dawley
  • Transforming Growth Factor beta1/drug effects
  • beta-Galactosidase/analysis

Cite this

Fluoride affects enamel protein content via TGF-β1-mediated KLK4 inhibition. / Suzuki, M; Shin, M; Simmer, J P; Bartlett, J D.

In: Journal of Dental Research, Vol. 93, No. 10, 10.2014, p. 1022-7.

Research output: Contribution to journalArticle

Suzuki, M ; Shin, M ; Simmer, J P ; Bartlett, J D. / Fluoride affects enamel protein content via TGF-β1-mediated KLK4 inhibition. In: Journal of Dental Research. 2014 ; Vol. 93, No. 10. pp. 1022-7.
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abstract = "Dental fluorosis is caused by chronic high-level fluoride (F(-)) exposure during enamel development, and fluorosed enamel has a higher than normal protein content. Matrix metalloproteinase 20 cleaves enamel matrix proteins during the secretory stage, and KLK4 further cleaves these proteins during the maturation stage so that the proteins can be reabsorbed from the hardening enamel. We show that transforming growth factor β1 (TGF-β1) can induce Klk4 expression, and we examine the effect of F(-) on TGF-β1 and KLK4 expression. We found that in vivo F(-) inhibits Klk4 but not Mmp20 transcript levels. LacZ-C57BL/6-Klk4 (+/LacZ) mice have LacZ inserted in frame at the Klk4 translation initiation site so that the endogenous Klk4 promoter drives LacZ expression in the same temporal/spatial way as it does for Klk4. KLK4 protein levels in rat enamel and β-galactosidase staining in LacZ-C57BL/6-Klk4 (+/LacZ) mouse enamel were both significantly reduced by F(-) treatment. Since TGF-β1 induces KLK4 expression, we tested and found that F(-) significantly reduced Tgf-β1 transcript levels in rat enamel organ. These data suggest that F(-)-mediated downregulation of TGF-β1 expression contributes to reduced KLK4 protein levels in fluorosed enamel and provides an explanation for why fluorosed enamel has a higher than normal protein content.",
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AU - Shin, M

AU - Simmer, J P

AU - Bartlett, J D

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N2 - Dental fluorosis is caused by chronic high-level fluoride (F(-)) exposure during enamel development, and fluorosed enamel has a higher than normal protein content. Matrix metalloproteinase 20 cleaves enamel matrix proteins during the secretory stage, and KLK4 further cleaves these proteins during the maturation stage so that the proteins can be reabsorbed from the hardening enamel. We show that transforming growth factor β1 (TGF-β1) can induce Klk4 expression, and we examine the effect of F(-) on TGF-β1 and KLK4 expression. We found that in vivo F(-) inhibits Klk4 but not Mmp20 transcript levels. LacZ-C57BL/6-Klk4 (+/LacZ) mice have LacZ inserted in frame at the Klk4 translation initiation site so that the endogenous Klk4 promoter drives LacZ expression in the same temporal/spatial way as it does for Klk4. KLK4 protein levels in rat enamel and β-galactosidase staining in LacZ-C57BL/6-Klk4 (+/LacZ) mouse enamel were both significantly reduced by F(-) treatment. Since TGF-β1 induces KLK4 expression, we tested and found that F(-) significantly reduced Tgf-β1 transcript levels in rat enamel organ. These data suggest that F(-)-mediated downregulation of TGF-β1 expression contributes to reduced KLK4 protein levels in fluorosed enamel and provides an explanation for why fluorosed enamel has a higher than normal protein content.

AB - Dental fluorosis is caused by chronic high-level fluoride (F(-)) exposure during enamel development, and fluorosed enamel has a higher than normal protein content. Matrix metalloproteinase 20 cleaves enamel matrix proteins during the secretory stage, and KLK4 further cleaves these proteins during the maturation stage so that the proteins can be reabsorbed from the hardening enamel. We show that transforming growth factor β1 (TGF-β1) can induce Klk4 expression, and we examine the effect of F(-) on TGF-β1 and KLK4 expression. We found that in vivo F(-) inhibits Klk4 but not Mmp20 transcript levels. LacZ-C57BL/6-Klk4 (+/LacZ) mice have LacZ inserted in frame at the Klk4 translation initiation site so that the endogenous Klk4 promoter drives LacZ expression in the same temporal/spatial way as it does for Klk4. KLK4 protein levels in rat enamel and β-galactosidase staining in LacZ-C57BL/6-Klk4 (+/LacZ) mouse enamel were both significantly reduced by F(-) treatment. Since TGF-β1 induces KLK4 expression, we tested and found that F(-) significantly reduced Tgf-β1 transcript levels in rat enamel organ. These data suggest that F(-)-mediated downregulation of TGF-β1 expression contributes to reduced KLK4 protein levels in fluorosed enamel and provides an explanation for why fluorosed enamel has a higher than normal protein content.

KW - Ameloblasts/drug effects

KW - Amelogenin/analysis

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KW - Cariostatic Agents/pharmacology

KW - Cell Line, Tumor

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KW - Down-Regulation

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KW - Fluorides/pharmacology

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KW - Mice

KW - Mice, Inbred C57BL

KW - Mice, Inbred Strains

KW - Rats

KW - Rats, Sprague-Dawley

KW - Transforming Growth Factor beta1/drug effects

KW - beta-Galactosidase/analysis

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VL - 93

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JO - Journal of Dental Research

JF - Journal of Dental Research

SN - 0022-0345

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