Induction of osteogenic markers in differentially treated cultures of embryonic stem cells

<p>Abstract</p> <p>Background</p> <p>Facial trauma or tumor surgery in the head and face area often lead to massive destruction of the facial skeleton. Cell-based bone reconstruction therapies promise to offer new therapeutic opportunities for the repair of bone damaged...

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Main Authors: Ommerborn Michelle A, Wiesmann Hans-Peter, Naujoks Christian, Kübler Norbert R, Depprich Rita A, Berr Karin, Handschel Jörg, Meyer Ulrich
Format: Article
Language:English
Published: BMC 2008-06-01
Series:Head & Face Medicine
Online Access:http://www.head-face-med.com/content/4/1/10
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spelling doaj-80f74e6ac01547c2845f601e5b7f395e2020-11-24T21:14:32ZengBMCHead & Face Medicine1746-160X2008-06-01411010.1186/1746-160X-4-10Induction of osteogenic markers in differentially treated cultures of embryonic stem cellsOmmerborn Michelle AWiesmann Hans-PeterNaujoks ChristianKübler Norbert RDepprich Rita ABerr KarinHandschel JörgMeyer Ulrich<p>Abstract</p> <p>Background</p> <p>Facial trauma or tumor surgery in the head and face area often lead to massive destruction of the facial skeleton. Cell-based bone reconstruction therapies promise to offer new therapeutic opportunities for the repair of bone damaged by disease or injury. Currently, embryonic stem cells (ESCs) are discussed to be a potential cell source for bone tissue engineering. The purpose of this study was to investigate various supplements in culture media with respect to the induction of osteogenic differentiation.</p> <p>Methods</p> <p>Murine ESCs were cultured in the presence of LIF (leukemia inhibitory factor), DAG (dexamethasone, ascorbic acid and β-glycerophosphate) or bone morphogenetic protein-2 (BMP-2). Microscopical analyses were performed using von Kossa staining, and expression of osteogenic marker genes was determined by real time PCR.</p> <p>Results</p> <p>ESCs cultured with DAG showed by far the largest deposition of calcium phosphate-containing minerals. Starting at day 9 of culture, a strong increase in collagen I mRNA expression was detected in the DAG-treated cells. In BMP-2-treated ESCs the collagen I mRNA induction was less increased. Expression of osteocalcin, a highly specific marker for osteogentic differentiation, showed a double-peaked curve in DAG-treated cells. ESCs cultured in the presence of DAG showed a strong increase in osteocalcin mRNA at day 9 followed by a second peak starting at day 17.</p> <p>Conclusion</p> <p>Supplementation of ESC cell cultures with DAG is effective in inducing osteogenic differentiation and appears to be more potent than stimulation with BMP-2 alone. Thus, DAG treatment can be recommended for generating ESC populations with osteogenic differentiation that are intended for use in bone tissue engineering.</p> http://www.head-face-med.com/content/4/1/10
collection DOAJ
language English
format Article
sources DOAJ
author Ommerborn Michelle A
Wiesmann Hans-Peter
Naujoks Christian
Kübler Norbert R
Depprich Rita A
Berr Karin
Handschel Jörg
Meyer Ulrich
spellingShingle Ommerborn Michelle A
Wiesmann Hans-Peter
Naujoks Christian
Kübler Norbert R
Depprich Rita A
Berr Karin
Handschel Jörg
Meyer Ulrich
Induction of osteogenic markers in differentially treated cultures of embryonic stem cells
Head & Face Medicine
author_facet Ommerborn Michelle A
Wiesmann Hans-Peter
Naujoks Christian
Kübler Norbert R
Depprich Rita A
Berr Karin
Handschel Jörg
Meyer Ulrich
author_sort Ommerborn Michelle A
title Induction of osteogenic markers in differentially treated cultures of embryonic stem cells
title_short Induction of osteogenic markers in differentially treated cultures of embryonic stem cells
title_full Induction of osteogenic markers in differentially treated cultures of embryonic stem cells
title_fullStr Induction of osteogenic markers in differentially treated cultures of embryonic stem cells
title_full_unstemmed Induction of osteogenic markers in differentially treated cultures of embryonic stem cells
title_sort induction of osteogenic markers in differentially treated cultures of embryonic stem cells
publisher BMC
series Head & Face Medicine
issn 1746-160X
publishDate 2008-06-01
description <p>Abstract</p> <p>Background</p> <p>Facial trauma or tumor surgery in the head and face area often lead to massive destruction of the facial skeleton. Cell-based bone reconstruction therapies promise to offer new therapeutic opportunities for the repair of bone damaged by disease or injury. Currently, embryonic stem cells (ESCs) are discussed to be a potential cell source for bone tissue engineering. The purpose of this study was to investigate various supplements in culture media with respect to the induction of osteogenic differentiation.</p> <p>Methods</p> <p>Murine ESCs were cultured in the presence of LIF (leukemia inhibitory factor), DAG (dexamethasone, ascorbic acid and β-glycerophosphate) or bone morphogenetic protein-2 (BMP-2). Microscopical analyses were performed using von Kossa staining, and expression of osteogenic marker genes was determined by real time PCR.</p> <p>Results</p> <p>ESCs cultured with DAG showed by far the largest deposition of calcium phosphate-containing minerals. Starting at day 9 of culture, a strong increase in collagen I mRNA expression was detected in the DAG-treated cells. In BMP-2-treated ESCs the collagen I mRNA induction was less increased. Expression of osteocalcin, a highly specific marker for osteogentic differentiation, showed a double-peaked curve in DAG-treated cells. ESCs cultured in the presence of DAG showed a strong increase in osteocalcin mRNA at day 9 followed by a second peak starting at day 17.</p> <p>Conclusion</p> <p>Supplementation of ESC cell cultures with DAG is effective in inducing osteogenic differentiation and appears to be more potent than stimulation with BMP-2 alone. Thus, DAG treatment can be recommended for generating ESC populations with osteogenic differentiation that are intended for use in bone tissue engineering.</p>
url http://www.head-face-med.com/content/4/1/10
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