Keratinocyte growth factor mRNA expression in periodontal ligament fibroblasts.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Keratinocyte growth factor mRNA expression in periodontal ligament fibroblasts. / Dabelsteen, S; Wandall, H H; Grøn, B; Dabelsteen, E.

I: European Journal of Oral Sciences, Bind 105, Nr. 6, 1997, s. 593-8.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Dabelsteen, S, Wandall, HH, Grøn, B & Dabelsteen, E 1997, 'Keratinocyte growth factor mRNA expression in periodontal ligament fibroblasts.', European Journal of Oral Sciences, bind 105, nr. 6, s. 593-8.

APA

Dabelsteen, S., Wandall, H. H., Grøn, B., & Dabelsteen, E. (1997). Keratinocyte growth factor mRNA expression in periodontal ligament fibroblasts. European Journal of Oral Sciences, 105(6), 593-8.

Vancouver

Dabelsteen S, Wandall HH, Grøn B, Dabelsteen E. Keratinocyte growth factor mRNA expression in periodontal ligament fibroblasts. European Journal of Oral Sciences. 1997;105(6):593-8.

Author

Dabelsteen, S ; Wandall, H H ; Grøn, B ; Dabelsteen, E. / Keratinocyte growth factor mRNA expression in periodontal ligament fibroblasts. I: European Journal of Oral Sciences. 1997 ; Bind 105, Nr. 6. s. 593-8.

Bibtex

@article{0ebb5480849e11dd81b0000ea68e967b,
title = "Keratinocyte growth factor mRNA expression in periodontal ligament fibroblasts.",
abstract = "Keratinocyte growth factor (KGF) is a fibroblast growth factor which mediates epithelial growth and differentiation. KGF is expressed in subepithelial fibroblasts, but generally not in fibroblasts of deep connective tissue, such as fascia and ligaments. Here we demonstrate that KGF mRNA is expressed in periodontal ligament fibroblasts, and that the expression is increased upon serum stimulation. Fibroblasts from human periodontal ligament, from buccal mucosa, from gingiva, and from skin were established from explants. Alkaline phosphatase activity was used as an indicator of the periodontal nature of fibroblasts. Cells were first cultured in DMEM with 0.5% fetal calf serum (FCS) and then incubated for 8 h, and 72 h in fresh DMEM with 10% FCS. Total RNA was isolated and used for Northern blotting with a P32-labeled KGF cDNA probe. Total RNA from cultured keratinocytes was used as negative controls. KGF mRNA was found in all cultured fibroblasts. Upon addition of 10% FCS to the cell cultures, an increase in KGF mRNA levels was noticed especially after 72 h. Furthermore, RT-PCR analysis of material scraped from the tooth root surface indicated the presence of KGF mRNA even in noncultured periodontal ligament cells.",
author = "S Dabelsteen and Wandall, {H H} and B Gr{\o}n and E Dabelsteen",
note = "Keywords: Adolescent; Adult; Alkaline Phosphatase; Blood; Blotting, Northern; Cell Differentiation; Cells, Cultured; Culture Media; DNA Probes; DNA, Complementary; Epithelial Cells; Epithelium; Female; Fibroblast Growth Factor 10; Fibroblast Growth Factor 7; Fibroblast Growth Factors; Fibroblasts; Gene Expression Regulation; Gingiva; Growth Substances; Humans; Mouth Mucosa; Periodontal Ligament; Phosphorus Radioisotopes; Polymerase Chain Reaction; RNA, Messenger; Radiopharmaceuticals; Skin; Time Factors; Tooth Root; Transcription, Genetic",
year = "1997",
language = "English",
volume = "105",
pages = "593--8",
journal = "European Journal of Oral Sciences",
issn = "0909-8836",
publisher = "Wiley-Blackwell",
number = "6",

}

RIS

TY - JOUR

T1 - Keratinocyte growth factor mRNA expression in periodontal ligament fibroblasts.

AU - Dabelsteen, S

AU - Wandall, H H

AU - Grøn, B

AU - Dabelsteen, E

N1 - Keywords: Adolescent; Adult; Alkaline Phosphatase; Blood; Blotting, Northern; Cell Differentiation; Cells, Cultured; Culture Media; DNA Probes; DNA, Complementary; Epithelial Cells; Epithelium; Female; Fibroblast Growth Factor 10; Fibroblast Growth Factor 7; Fibroblast Growth Factors; Fibroblasts; Gene Expression Regulation; Gingiva; Growth Substances; Humans; Mouth Mucosa; Periodontal Ligament; Phosphorus Radioisotopes; Polymerase Chain Reaction; RNA, Messenger; Radiopharmaceuticals; Skin; Time Factors; Tooth Root; Transcription, Genetic

PY - 1997

Y1 - 1997

N2 - Keratinocyte growth factor (KGF) is a fibroblast growth factor which mediates epithelial growth and differentiation. KGF is expressed in subepithelial fibroblasts, but generally not in fibroblasts of deep connective tissue, such as fascia and ligaments. Here we demonstrate that KGF mRNA is expressed in periodontal ligament fibroblasts, and that the expression is increased upon serum stimulation. Fibroblasts from human periodontal ligament, from buccal mucosa, from gingiva, and from skin were established from explants. Alkaline phosphatase activity was used as an indicator of the periodontal nature of fibroblasts. Cells were first cultured in DMEM with 0.5% fetal calf serum (FCS) and then incubated for 8 h, and 72 h in fresh DMEM with 10% FCS. Total RNA was isolated and used for Northern blotting with a P32-labeled KGF cDNA probe. Total RNA from cultured keratinocytes was used as negative controls. KGF mRNA was found in all cultured fibroblasts. Upon addition of 10% FCS to the cell cultures, an increase in KGF mRNA levels was noticed especially after 72 h. Furthermore, RT-PCR analysis of material scraped from the tooth root surface indicated the presence of KGF mRNA even in noncultured periodontal ligament cells.

AB - Keratinocyte growth factor (KGF) is a fibroblast growth factor which mediates epithelial growth and differentiation. KGF is expressed in subepithelial fibroblasts, but generally not in fibroblasts of deep connective tissue, such as fascia and ligaments. Here we demonstrate that KGF mRNA is expressed in periodontal ligament fibroblasts, and that the expression is increased upon serum stimulation. Fibroblasts from human periodontal ligament, from buccal mucosa, from gingiva, and from skin were established from explants. Alkaline phosphatase activity was used as an indicator of the periodontal nature of fibroblasts. Cells were first cultured in DMEM with 0.5% fetal calf serum (FCS) and then incubated for 8 h, and 72 h in fresh DMEM with 10% FCS. Total RNA was isolated and used for Northern blotting with a P32-labeled KGF cDNA probe. Total RNA from cultured keratinocytes was used as negative controls. KGF mRNA was found in all cultured fibroblasts. Upon addition of 10% FCS to the cell cultures, an increase in KGF mRNA levels was noticed especially after 72 h. Furthermore, RT-PCR analysis of material scraped from the tooth root surface indicated the presence of KGF mRNA even in noncultured periodontal ligament cells.

M3 - Journal article

C2 - 9469611

VL - 105

SP - 593

EP - 598

JO - European Journal of Oral Sciences

JF - European Journal of Oral Sciences

SN - 0909-8836

IS - 6

ER -

ID: 6092087