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CELL PROLIFERATION AND CYTOKINE INDUCTION BY TNF-α OF PSORIATIC KERATINOCYTES ARE NOT DIFFERENT FROM NORMAL KERATINOCYTES IN VITRO

BACKGROUND: Recent studies indicate that various cytokines including tumor necrosis factor-α (TNF-α) play an essential role in the induction and maintenance of psoriatic lesion. AIMS: To compare the cell proliferation of keratinocytes by various cytokines and TNF-α-induced cytokine secretion among n...

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Autores principales: Takahashi, Hidetoshi, Tsuji, Hitomi, Hashimoto, Yoshio, Ishida-Yamamoto, Akemi, Iizuka, Hajime
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2810688/
https://www.ncbi.nlm.nih.gov/pubmed/20161853
http://dx.doi.org/10.4103/0019-5154.55631
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author Takahashi, Hidetoshi
Tsuji, Hitomi
Hashimoto, Yoshio
Ishida-Yamamoto, Akemi
Iizuka, Hajime
author_facet Takahashi, Hidetoshi
Tsuji, Hitomi
Hashimoto, Yoshio
Ishida-Yamamoto, Akemi
Iizuka, Hajime
author_sort Takahashi, Hidetoshi
collection PubMed
description BACKGROUND: Recent studies indicate that various cytokines including tumor necrosis factor-α (TNF-α) play an essential role in the induction and maintenance of psoriatic lesion. AIMS: To compare the cell proliferation of keratinocytes by various cytokines and TNF-α-induced cytokine secretion among normal keratinocytes, uninvolved, and involved keratinocytes. METHODS: The keratinocytes from normal skin, uninvolved, and involved psoriasis were cultured in the presence of IL-6, IL-8, epidermal growth factor (EGF), hepatocyte growth factor (HGF), transforming growth factor-α (TGF-α) epiregulin, amphiregulin, and TNF-α and then MTT assay for keratinocytes proliferation was performed. Furthermore, TNF-α-induced secretion of IL-6, IL-8, EGF, HGF, TGF-α, epiregulin, and amphiregulin were compared among these keratinocytes. RESULTS: IL-6, IL-8, EFG, TGF-α, epiregulin, and amphiregulin, but not TNF-α increased keratinocyte proliferation of normal, psoriatic uninvolved, and involved skin. The increased cell proliferation by these cytokines and growth factors were not different among the keratinocytes derived from normal skin, uninvolved, and involved psoriasis. The significant induction of TNF-α increased IL-6, IL-8, EGF, HGF, TGF-α, epiregulin, and amphiregulin, but the increase in these cytokines and growth factors were not different among normal skin, uninvolved, and involved psoriasis. CONCLUSION: Cell proliferation by various cytokines and growth factors and TNF-α-induced cytokine secretion are not different between normal and psoriatic keratinocytes.
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spelling pubmed-28106882010-02-16 CELL PROLIFERATION AND CYTOKINE INDUCTION BY TNF-α OF PSORIATIC KERATINOCYTES ARE NOT DIFFERENT FROM NORMAL KERATINOCYTES IN VITRO Takahashi, Hidetoshi Tsuji, Hitomi Hashimoto, Yoshio Ishida-Yamamoto, Akemi Iizuka, Hajime Indian J Dermatol Basic Research BACKGROUND: Recent studies indicate that various cytokines including tumor necrosis factor-α (TNF-α) play an essential role in the induction and maintenance of psoriatic lesion. AIMS: To compare the cell proliferation of keratinocytes by various cytokines and TNF-α-induced cytokine secretion among normal keratinocytes, uninvolved, and involved keratinocytes. METHODS: The keratinocytes from normal skin, uninvolved, and involved psoriasis were cultured in the presence of IL-6, IL-8, epidermal growth factor (EGF), hepatocyte growth factor (HGF), transforming growth factor-α (TGF-α) epiregulin, amphiregulin, and TNF-α and then MTT assay for keratinocytes proliferation was performed. Furthermore, TNF-α-induced secretion of IL-6, IL-8, EGF, HGF, TGF-α, epiregulin, and amphiregulin were compared among these keratinocytes. RESULTS: IL-6, IL-8, EFG, TGF-α, epiregulin, and amphiregulin, but not TNF-α increased keratinocyte proliferation of normal, psoriatic uninvolved, and involved skin. The increased cell proliferation by these cytokines and growth factors were not different among the keratinocytes derived from normal skin, uninvolved, and involved psoriasis. The significant induction of TNF-α increased IL-6, IL-8, EGF, HGF, TGF-α, epiregulin, and amphiregulin, but the increase in these cytokines and growth factors were not different among normal skin, uninvolved, and involved psoriasis. CONCLUSION: Cell proliferation by various cytokines and growth factors and TNF-α-induced cytokine secretion are not different between normal and psoriatic keratinocytes. Medknow Publications 2009 /pmc/articles/PMC2810688/ /pubmed/20161853 http://dx.doi.org/10.4103/0019-5154.55631 Text en © Indian Journal of Dermatology http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Basic Research
Takahashi, Hidetoshi
Tsuji, Hitomi
Hashimoto, Yoshio
Ishida-Yamamoto, Akemi
Iizuka, Hajime
CELL PROLIFERATION AND CYTOKINE INDUCTION BY TNF-α OF PSORIATIC KERATINOCYTES ARE NOT DIFFERENT FROM NORMAL KERATINOCYTES IN VITRO
title CELL PROLIFERATION AND CYTOKINE INDUCTION BY TNF-α OF PSORIATIC KERATINOCYTES ARE NOT DIFFERENT FROM NORMAL KERATINOCYTES IN VITRO
title_full CELL PROLIFERATION AND CYTOKINE INDUCTION BY TNF-α OF PSORIATIC KERATINOCYTES ARE NOT DIFFERENT FROM NORMAL KERATINOCYTES IN VITRO
title_fullStr CELL PROLIFERATION AND CYTOKINE INDUCTION BY TNF-α OF PSORIATIC KERATINOCYTES ARE NOT DIFFERENT FROM NORMAL KERATINOCYTES IN VITRO
title_full_unstemmed CELL PROLIFERATION AND CYTOKINE INDUCTION BY TNF-α OF PSORIATIC KERATINOCYTES ARE NOT DIFFERENT FROM NORMAL KERATINOCYTES IN VITRO
title_short CELL PROLIFERATION AND CYTOKINE INDUCTION BY TNF-α OF PSORIATIC KERATINOCYTES ARE NOT DIFFERENT FROM NORMAL KERATINOCYTES IN VITRO
title_sort cell proliferation and cytokine induction by tnf-α of psoriatic keratinocytes are not different from normal keratinocytes in vitro
topic Basic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2810688/
https://www.ncbi.nlm.nih.gov/pubmed/20161853
http://dx.doi.org/10.4103/0019-5154.55631
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