Gene expression of markers associated with proliferation and differentiation in human keratinocytes cultured from epidermis and from buccal mucosa

Normal keratinocytes from epidermis and from buccal mucosa underwent dissimilar stages of differentiation in the same culture medium and responded differently to changes in the composition of the medium. Manifestations of these variations were examined in terms of the expression at the mRNA level (a...

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Published inArchives of oral biology Vol. 40; no. 9; pp. 855 - 862
Main Authors Brysk, Miriam M., Arany, Istvan, Brysk, Henry, Chen, San-Hwan, Calhoun, Karen H., Tyring, Stephen K.
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.09.1995
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Abstract Normal keratinocytes from epidermis and from buccal mucosa underwent dissimilar stages of differentiation in the same culture medium and responded differently to changes in the composition of the medium. Manifestations of these variations were examined in terms of the expression at the mRNA level (as measured by reverse transcriptase-polymerase chain reaction) of three regulatory genes (cdc2, c- myc, and p53) and five genes that encode structural proteins (keratins K5, K10 and K13, involucrin, and filaggrin), in three growth-medium formulations. The culture conditions enhanced or retarded maturation; the observed alterations in gene expression correlated with these changes. Except for the proliferation genes, the non-keratinizing buccal mucosa generally responded more weakly than the orthokeratotic epidermis to culture-medium supplementation favouring differentiation. Gene expression in cultured keratinocytes reflected their ability to differentiate in vivo; genes were expressed even when the corresponding protein was not seen in vitro. Although keratin K10 is not prevalent in the buccal mucosa nor keratin K13 in the epidermis, the genes for both were found to be expressed in both tissues.
AbstractList Normal keratinocytes from epidermis and from buccal mucosa underwent dissimilar stages of differentiation in the same culture medium and responded differently to changes in the composition of the medium. Manifestations of these variations were examined in terms of the expression at the mRNA level (as measured by reverse transcriptase-polymerase chain reaction) of three regulatory genes (cdc2, c- myc, and p53) and five genes that encode structural proteins (keratins K5, K10 and K13, involucrin, and filaggrin), in three growth-medium formulations. The culture conditions enhanced or retarded maturation; the observed alterations in gene expression correlated with these changes. Except for the proliferation genes, the non-keratinizing buccal mucosa generally responded more weakly than the orthokeratotic epidermis to culture-medium supplementation favouring differentiation. Gene expression in cultured keratinocytes reflected their ability to differentiate in vivo; genes were expressed even when the corresponding protein was not seen in vitro. Although keratin K10 is not prevalent in the buccal mucosa nor keratin K13 in the epidermis, the genes for both were found to be expressed in both tissues.
Normal keratinocytes from epidermis and from buccal mucosa underwent dissimilar stages of differentiation in the same culture medium and responded differently to changes in the composition of the medium. Manifestations of these variations were examined in terms of the expression at the mRNA level (as measured by reverse transcriptase-polymerase chain reaction) of three regulatory genes (cdc2, c-myc, and p53) and five that encode structural proteins (keratins K5, K10 and K13, involucrin, and filaggrin), in three growth-medium formulations. The culture conditions enhanced or retarded maturation; the observed alterations in gene expression correlated with these changes. Except for the proliferation genes, the non-keratinizing buccal mucosa generally responded more weakly than the orthokeratotic epidermis to culture-medium supplementation favouring differentiation. Gene expression in cultured keratinocytes reflected their ability to differentiate in vivo; genes were expressed even when the corresponding protein was not seen in vitro. Although keratin K10 is not prevalent in the buccal mucosa nor keratin K13 in the epidermis, the genes for both were found to be expressed in both tissues.
Author Brysk, Henry
Chen, San-Hwan
Calhoun, Karen H.
Tyring, Stephen K.
Brysk, Miriam M.
Arany, Istvan
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Issue 9
Keywords buccal mucosa
differentiation
RT-PCR, reverse transcriptase-polymerase chain reaction
keratinocytes
keratins
involucrin
p53
c- myc
G3PDH, glyceraldehyde-3-phosphate dehydrogenase
filaggrin
gene expression
cdc2
epidermis
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  start-page: 171
  year: 1988
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  article-title: Biological mechanisms for the regulation of normal human keratinocyte proliferation and differentiation
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  start-page: 261
  year: 1986
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  article-title: Granulocyte colony stimulating activity derived from human keratinocytes
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Snippet Normal keratinocytes from epidermis and from buccal mucosa underwent dissimilar stages of differentiation in the same culture medium and responded differently...
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SubjectTerms buccal mucosa
c- myc
Calcium
cdc2
Cell Differentiation - genetics
Cell Division - genetics
Cells, Cultured
Culture Media
Culture Media, Serum-Free
Dentistry
differentiation
Epidermal Cells
epidermis
Epidermis - metabolism
filaggrin
gene expression
Gene Expression Regulation
Gene Expression Regulation, Enzymologic
Genes, cdc - genetics
Genes, myc - genetics
Genes, p53 - genetics
Glyceraldehyde-3-Phosphate Dehydrogenases - genetics
Humans
Intermediate Filament Proteins - genetics
involucrin
keratinocytes
Keratinocytes - cytology
Keratinocytes - metabolism
keratins
Keratins - genetics
Mouth Mucosa - cytology
Mouth Mucosa - metabolism
p53
Polymerase Chain Reaction
Protein Precursors - genetics
RNA, Messenger - genetics
Transcription, Genetic
Title Gene expression of markers associated with proliferation and differentiation in human keratinocytes cultured from epidermis and from buccal mucosa
URI https://dx.doi.org/10.1016/0003-9969(95)00046-R
https://www.ncbi.nlm.nih.gov/pubmed/8651890
https://search.proquest.com/docview/77751890
Volume 40
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