Basic fibroblast growth factor: a potential new therapeutic tool for the treatment of hypertrophic and keloid scars

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Basic fibroblast growth factor: a potential new therapeutic tool for the treatment of hypertrophic and keloid scars. / Tiede, Stephan; Ernst, Nancy; Bayat, Ardeshir; Paus, Ralf; Tronnier, Volker; Zechel, Christina.

In: ANN ANAT, Vol. 191, No. 1, 01.2009, p. 33-44.

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@article{e5cee926225d471f95f025d7a5fdd84c,
title = "Basic fibroblast growth factor: a potential new therapeutic tool for the treatment of hypertrophic and keloid scars",
abstract = "Numerous tissue niches in the human body, such as skin, are now recognized to harbour adult stem cells. In this study, we analyze multipotent human dermis-derived progenitor cell populations, isolated and propagated from mechanically and enzymatically processed adult scalp skin. The populations encompass Nestin-positive and -negative cells, which may serve as a convenient and abundant source for various therapeutic applications in regenerative medicine. Here, we show that these cultures exhibit a strong tendency to differentiate into mesodermal derivatives, particularly myofibroblasts, when maintained in media containing serum. Since undesired and excessive myofibroblast formation is a frequent postsurgical complication, we sought culture conditions that would prevent myofibroblast formation. In particular, we analyzed the effect of growth factors, such as epidermal growth factor (EGF), basic fibroblast growth factor (bFGF), and platelet-derived growth factor AB (PDGF AB). Our results demonstrate that bFGF is a potent inhibitor of mesodermal differentiation, whereas PDFG AB favours myofibroblast formation and up-regulates expression of TGFbeta receptors I and II. This interesting discovery may help in the prevention and treatment of tissue fibrosis and in particular in the eradication of hypertrophic and keloid scars.",
keywords = "Cell Culture Techniques, Cell Differentiation, Cicatrix, Dermis, Epidermal Growth Factor, Fibroblast Growth Factor 2, Humans, Hypertrophy, Immunohistochemistry, Keloid, Platelet-Derived Growth Factor, Regeneration, Reverse Transcriptase Polymerase Chain Reaction, Stem Cells, Transforming Growth Factor beta, Journal Article",
author = "Stephan Tiede and Nancy Ernst and Ardeshir Bayat and Ralf Paus and Volker Tronnier and Christina Zechel",
year = "2009",
month = jan,
doi = "10.1016/j.aanat.2008.10.001",
language = "English",
volume = "191",
pages = "33--44",
journal = "ANN ANAT",
issn = "0940-9602",
publisher = "Urban und Fischer Verlag Jena",
number = "1",

}

RIS

TY - JOUR

T1 - Basic fibroblast growth factor: a potential new therapeutic tool for the treatment of hypertrophic and keloid scars

AU - Tiede, Stephan

AU - Ernst, Nancy

AU - Bayat, Ardeshir

AU - Paus, Ralf

AU - Tronnier, Volker

AU - Zechel, Christina

PY - 2009/1

Y1 - 2009/1

N2 - Numerous tissue niches in the human body, such as skin, are now recognized to harbour adult stem cells. In this study, we analyze multipotent human dermis-derived progenitor cell populations, isolated and propagated from mechanically and enzymatically processed adult scalp skin. The populations encompass Nestin-positive and -negative cells, which may serve as a convenient and abundant source for various therapeutic applications in regenerative medicine. Here, we show that these cultures exhibit a strong tendency to differentiate into mesodermal derivatives, particularly myofibroblasts, when maintained in media containing serum. Since undesired and excessive myofibroblast formation is a frequent postsurgical complication, we sought culture conditions that would prevent myofibroblast formation. In particular, we analyzed the effect of growth factors, such as epidermal growth factor (EGF), basic fibroblast growth factor (bFGF), and platelet-derived growth factor AB (PDGF AB). Our results demonstrate that bFGF is a potent inhibitor of mesodermal differentiation, whereas PDFG AB favours myofibroblast formation and up-regulates expression of TGFbeta receptors I and II. This interesting discovery may help in the prevention and treatment of tissue fibrosis and in particular in the eradication of hypertrophic and keloid scars.

AB - Numerous tissue niches in the human body, such as skin, are now recognized to harbour adult stem cells. In this study, we analyze multipotent human dermis-derived progenitor cell populations, isolated and propagated from mechanically and enzymatically processed adult scalp skin. The populations encompass Nestin-positive and -negative cells, which may serve as a convenient and abundant source for various therapeutic applications in regenerative medicine. Here, we show that these cultures exhibit a strong tendency to differentiate into mesodermal derivatives, particularly myofibroblasts, when maintained in media containing serum. Since undesired and excessive myofibroblast formation is a frequent postsurgical complication, we sought culture conditions that would prevent myofibroblast formation. In particular, we analyzed the effect of growth factors, such as epidermal growth factor (EGF), basic fibroblast growth factor (bFGF), and platelet-derived growth factor AB (PDGF AB). Our results demonstrate that bFGF is a potent inhibitor of mesodermal differentiation, whereas PDFG AB favours myofibroblast formation and up-regulates expression of TGFbeta receptors I and II. This interesting discovery may help in the prevention and treatment of tissue fibrosis and in particular in the eradication of hypertrophic and keloid scars.

KW - Cell Culture Techniques

KW - Cell Differentiation

KW - Cicatrix

KW - Dermis

KW - Epidermal Growth Factor

KW - Fibroblast Growth Factor 2

KW - Humans

KW - Hypertrophy

KW - Immunohistochemistry

KW - Keloid

KW - Platelet-Derived Growth Factor

KW - Regeneration

KW - Reverse Transcriptase Polymerase Chain Reaction

KW - Stem Cells

KW - Transforming Growth Factor beta

KW - Journal Article

U2 - 10.1016/j.aanat.2008.10.001

DO - 10.1016/j.aanat.2008.10.001

M3 - SCORING: Journal article

C2 - 19071002

VL - 191

SP - 33

EP - 44

JO - ANN ANAT

JF - ANN ANAT

SN - 0940-9602

IS - 1

ER -