Inhibition of chondrogenic differentiation in chick limb-bud mesenchyme microcultures treated with cyclosporine
Objectives: To explore the effects of cyclosporine (CsA) on skeletal development (chondrogenesis). Materials and Methods: Mesenchymal cells obtained from stage-23 to stage-24 chick-embryo limb buds were grown in 96-well plates using chemically defined tissue-culture medium. Cultures were treated wit...
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description | Objectives: To explore the effects of cyclosporine (CsA) on skeletal
development (chondrogenesis). Materials and Methods: Mesenchymal cells
obtained from stage-23 to stage-24 chick-embryo limb buds were grown in
96-well plates using chemically defined tissue-culture medium. Cultures
were treated with CsA (0.01-5.0 μg/ml) and incubated (37°C,
5% CO2) with daily medium changes for 4 days. After incubation of the
cells in multiwell plate, cartilage differentiation (chondrogenesis)
was assessed by selectively staining sulfated glycosaminoglycans (GAGs)
in the cartilage matrix with Alcian blue, extracting the GAGs with 4 M
guanidinium HCl, and spectrophotometric analysis of the extracts.
Results: CsA treatment had concentration-dependent effects on chick
limb-bud mesenchymal cell cultures. At 5 μg/ml, CsA caused cell
loss, as judged microscopically by the paucity of cells remaining at
the end of the culture period. CsA concentrations between 0.1 and 1
μg/ml caused a marked, dose-dependent decrease in chondrogenesis.
At 0.01 μg/ml, CsA had no significant effect on chondrogenesis. At
concentrations above 0.01 μg/ml, normalized data showed
significant chondrogenic inhibition at 0.5 and 1.0 μg/ml CsA.
Conclusions: The findings suggest a possible biological basis for
CsA-associated effects on mesenchyme-derived tissues and provide a
model system for further studies. |
doi_str_mv | 10.4103/0253-7613.19852 |
format | Article |
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development (chondrogenesis). Materials and Methods: Mesenchymal cells
obtained from stage-23 to stage-24 chick-embryo limb buds were grown in
96-well plates using chemically defined tissue-culture medium. Cultures
were treated with CsA (0.01-5.0 μg/ml) and incubated (37°C,
5% CO2) with daily medium changes for 4 days. After incubation of the
cells in multiwell plate, cartilage differentiation (chondrogenesis)
was assessed by selectively staining sulfated glycosaminoglycans (GAGs)
in the cartilage matrix with Alcian blue, extracting the GAGs with 4 M
guanidinium HCl, and spectrophotometric analysis of the extracts.
Results: CsA treatment had concentration-dependent effects on chick
limb-bud mesenchymal cell cultures. At 5 μg/ml, CsA caused cell
loss, as judged microscopically by the paucity of cells remaining at
the end of the culture period. CsA concentrations between 0.1 and 1
μg/ml caused a marked, dose-dependent decrease in chondrogenesis.
At 0.01 μg/ml, CsA had no significant effect on chondrogenesis. At
concentrations above 0.01 μg/ml, normalized data showed
significant chondrogenic inhibition at 0.5 and 1.0 μg/ml CsA.
Conclusions: The findings suggest a possible biological basis for
CsA-associated effects on mesenchyme-derived tissues and provide a
model system for further studies.</description><identifier>ISSN: 0253-7613</identifier><identifier>EISSN: 1998-3751</identifier><identifier>DOI: 10.4103/0253-7613.19852</identifier><language>eng</language><publisher>Pondicherry: Medknow Publications on behalf of Indian Pharmacological Society</publisher><subject>Chondrogenesis, skeletal development spectrophotometric analysis ; Cyclosporine ; Glycosaminoglycans ; Immunosuppressive agents ; Pharmacology, Experimental</subject><ispartof>Indian journal of pharmacology, 2006, Vol.38 (1), p.43</ispartof><rights>Copyright 2006 Indian Journal of Pharmacology.</rights><rights>COPYRIGHT 2006 Medknow Publications and Media Pvt. Ltd.</rights><rights>Copyright Medknow Publications Jan/Feb 2006</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b3402-4e88b28f9214413ae2e1553282e6088fcbb766ca5ee5bb04a226e9213361e7273</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925,79426</link.rule.ids></links><search><creatorcontrib>Bahmanpour Soghra, Paulsen DouglasF</creatorcontrib><title>Inhibition of chondrogenic differentiation in chick limb-bud mesenchyme microcultures treated with cyclosporine</title><title>Indian journal of pharmacology</title><description>Objectives: To explore the effects of cyclosporine (CsA) on skeletal
development (chondrogenesis). Materials and Methods: Mesenchymal cells
obtained from stage-23 to stage-24 chick-embryo limb buds were grown in
96-well plates using chemically defined tissue-culture medium. Cultures
were treated with CsA (0.01-5.0 μg/ml) and incubated (37°C,
5% CO2) with daily medium changes for 4 days. After incubation of the
cells in multiwell plate, cartilage differentiation (chondrogenesis)
was assessed by selectively staining sulfated glycosaminoglycans (GAGs)
in the cartilage matrix with Alcian blue, extracting the GAGs with 4 M
guanidinium HCl, and spectrophotometric analysis of the extracts.
Results: CsA treatment had concentration-dependent effects on chick
limb-bud mesenchymal cell cultures. At 5 μg/ml, CsA caused cell
loss, as judged microscopically by the paucity of cells remaining at
the end of the culture period. CsA concentrations between 0.1 and 1
μg/ml caused a marked, dose-dependent decrease in chondrogenesis.
At 0.01 μg/ml, CsA had no significant effect on chondrogenesis. At
concentrations above 0.01 μg/ml, normalized data showed
significant chondrogenic inhibition at 0.5 and 1.0 μg/ml CsA.
Conclusions: The findings suggest a possible biological basis for
CsA-associated effects on mesenchyme-derived tissues and provide a
model system for further studies.</description><subject>Chondrogenesis, skeletal development spectrophotometric analysis</subject><subject>Cyclosporine</subject><subject>Glycosaminoglycans</subject><subject>Immunosuppressive agents</subject><subject>Pharmacology, Experimental</subject><issn>0253-7613</issn><issn>1998-3751</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>RBI</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptUU1r3DAQFSWBbpKeexW9e6MPf8jHENomEMglOQtJHsWT2tJWsin776vNhs0lSCA0770Z5j1CvnO2rTmT10w0supaLre8V434Qja871Ulu4afkc0J_Uoucn5l5V_37YbE-zCixQVjoNFTN8YwpPgCAR0d0HtIEBY0bziGgqP7QyecbWXXgc6QIbhxPwOd0aXo1mlZE2S6JDALDPQfLiN1ezfFvIsJA1yRc2-mDN_e30vy_Ovn0-1d9fD4-_725qGysmaiqkEpK5TvBa9rLg0I4E0jhRLQMqW8s7ZrW2cagMZaVhshWihkKVsOnejkJflx7LtL8e8KedGvcU2hjNS8b1THJOOFVB1JL2YCjcHHJRlXlodkphjAYynf8FpIUWw8NN1-wi9ngLL-p4Lro6B4k3MCr3cJZ5P2mjN9SE0fctGHXPRbah8jLMap-HUSuIRGn4pjuaxlTMn_vM2bQQ</recordid><startdate>2006</startdate><enddate>2006</enddate><creator>Bahmanpour Soghra, Paulsen DouglasF</creator><general>Medknow Publications on behalf of Indian Pharmacological Society</general><general>Medknow Publications and Media Pvt. Ltd</general><general>Medknow Publications & Media Pvt. Ltd</general><scope>RBI</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope></search><sort><creationdate>2006</creationdate><title>Inhibition of chondrogenic differentiation in chick limb-bud mesenchyme microcultures treated with cyclosporine</title><author>Bahmanpour Soghra, Paulsen DouglasF</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b3402-4e88b28f9214413ae2e1553282e6088fcbb766ca5ee5bb04a226e9213361e7273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Chondrogenesis, skeletal development spectrophotometric analysis</topic><topic>Cyclosporine</topic><topic>Glycosaminoglycans</topic><topic>Immunosuppressive agents</topic><topic>Pharmacology, Experimental</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bahmanpour Soghra, Paulsen DouglasF</creatorcontrib><collection>Bioline International</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><jtitle>Indian journal of pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bahmanpour Soghra, Paulsen DouglasF</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inhibition of chondrogenic differentiation in chick limb-bud mesenchyme microcultures treated with cyclosporine</atitle><jtitle>Indian journal of pharmacology</jtitle><date>2006</date><risdate>2006</risdate><volume>38</volume><issue>1</issue><spage>43</spage><pages>43-</pages><issn>0253-7613</issn><eissn>1998-3751</eissn><abstract>Objectives: To explore the effects of cyclosporine (CsA) on skeletal
development (chondrogenesis). Materials and Methods: Mesenchymal cells
obtained from stage-23 to stage-24 chick-embryo limb buds were grown in
96-well plates using chemically defined tissue-culture medium. Cultures
were treated with CsA (0.01-5.0 μg/ml) and incubated (37°C,
5% CO2) with daily medium changes for 4 days. After incubation of the
cells in multiwell plate, cartilage differentiation (chondrogenesis)
was assessed by selectively staining sulfated glycosaminoglycans (GAGs)
in the cartilage matrix with Alcian blue, extracting the GAGs with 4 M
guanidinium HCl, and spectrophotometric analysis of the extracts.
Results: CsA treatment had concentration-dependent effects on chick
limb-bud mesenchymal cell cultures. At 5 μg/ml, CsA caused cell
loss, as judged microscopically by the paucity of cells remaining at
the end of the culture period. CsA concentrations between 0.1 and 1
μg/ml caused a marked, dose-dependent decrease in chondrogenesis.
At 0.01 μg/ml, CsA had no significant effect on chondrogenesis. At
concentrations above 0.01 μg/ml, normalized data showed
significant chondrogenic inhibition at 0.5 and 1.0 μg/ml CsA.
Conclusions: The findings suggest a possible biological basis for
CsA-associated effects on mesenchyme-derived tissues and provide a
model system for further studies.</abstract><cop>Pondicherry</cop><pub>Medknow Publications on behalf of Indian Pharmacological Society</pub><doi>10.4103/0253-7613.19852</doi><oa>free_for_read</oa></addata></record> |
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source | Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Bioline International; Free Full-Text Journals in Chemistry |
subjects | Chondrogenesis, skeletal development spectrophotometric analysis Cyclosporine Glycosaminoglycans Immunosuppressive agents Pharmacology, Experimental |
title | Inhibition of chondrogenic differentiation in chick limb-bud mesenchyme microcultures treated with cyclosporine |
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