Evaluation of serum‐free differentiation conditions for C2C12 myoblast cells assessed as to active tension generation capability
We have compared several serum‐free media for the differentiation of C2C12 myoblasts and assessed the extent of differentiation in several ways including as to active tension generation capability. C2C12 cells were allowed to differentiate in Dulbecco's modified Eagle's medium (DMEM) conta...
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| Veröffentlicht in: | Biotechnology and bioengineering 2010-12, Vol.107 (5), p.894-901 |
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| creator | Fujita, Hideaki Endo, Akiko Shimizu, Kazunori Nagamori, Eiji |
| description | We have compared several serum‐free media for the differentiation of C2C12 myoblasts and assessed the extent of differentiation in several ways including as to active tension generation capability. C2C12 cells were allowed to differentiate in Dulbecco's modified Eagle's medium (DMEM) containing Ham's F‐12 (F‐12), AIM‐V (AIM), 0.2% Ultroser‐G in DMEM (Ult‐G), and 0.1% Sericin in DMEM (Sericin), compared with in DMEM supplemented with 2% horse serum (HS) or 2% calf serum (CS). C2C12 differentiation was assessed as the extent of myotube formation, glucose metabolism, protein expression, sarcomere formation, and active tension generation. All serum‐free media examined were capable of inducing myotube formation and the expression of muscle‐specific proteins. All serum‐free media except for F‐12 gave the sarcomere structure. Active tension generation was observed for cells that differentiated in AIM and Ult‐G, but the active tension generated by C2C12 cells that differentiated in Ult‐G was only ∼25% in the case of myotubes that formed in HS. The addition of Ult‐G to the AIM resulted in improvement of the active tension generation capability, the active tension generated being ∼3.4× compared to that in HS. The approach for assessing muscle cell differentiation presented in this study will be suitable for other studies that involve the differentiation of muscle cells. Biotechnol. Bioeng. 2010;107: 894-901. |
| doi_str_mv | 10.1002/bit.22865 |
| format | Article |
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C2C12 cells were allowed to differentiate in Dulbecco's modified Eagle's medium (DMEM) containing Ham's F‐12 (F‐12), AIM‐V (AIM), 0.2% Ultroser‐G in DMEM (Ult‐G), and 0.1% Sericin in DMEM (Sericin), compared with in DMEM supplemented with 2% horse serum (HS) or 2% calf serum (CS). C2C12 differentiation was assessed as the extent of myotube formation, glucose metabolism, protein expression, sarcomere formation, and active tension generation. All serum‐free media examined were capable of inducing myotube formation and the expression of muscle‐specific proteins. All serum‐free media except for F‐12 gave the sarcomere structure. Active tension generation was observed for cells that differentiated in AIM and Ult‐G, but the active tension generated by C2C12 cells that differentiated in Ult‐G was only ∼25% in the case of myotubes that formed in HS. The addition of Ult‐G to the AIM resulted in improvement of the active tension generation capability, the active tension generated being ∼3.4× compared to that in HS. The approach for assessing muscle cell differentiation presented in this study will be suitable for other studies that involve the differentiation of muscle cells. Biotechnol. Bioeng. 2010;107: 894-901.</description><identifier>ISSN: 0006-3592</identifier><identifier>ISSN: 1097-0290</identifier><identifier>EISSN: 1097-0290</identifier><identifier>DOI: 10.1002/bit.22865</identifier><identifier>PMID: 20635352</identifier><identifier>CODEN: BIBIAU</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>AIM-V ; Animals ; Biological and medical sciences ; Biotechnology ; C2C12 ; Cell Differentiation ; Cells ; Culture Media - chemistry ; Culture Media, Serum-Free ; Differentiation ; F-12 ; Fundamental and applied biological sciences. Psychology ; Gene expression ; Glucose ; Ham ; Health. Pharmaceutical industry ; Industrial applications and implications. 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Bioeng</addtitle><description>We have compared several serum‐free media for the differentiation of C2C12 myoblasts and assessed the extent of differentiation in several ways including as to active tension generation capability. C2C12 cells were allowed to differentiate in Dulbecco's modified Eagle's medium (DMEM) containing Ham's F‐12 (F‐12), AIM‐V (AIM), 0.2% Ultroser‐G in DMEM (Ult‐G), and 0.1% Sericin in DMEM (Sericin), compared with in DMEM supplemented with 2% horse serum (HS) or 2% calf serum (CS). C2C12 differentiation was assessed as the extent of myotube formation, glucose metabolism, protein expression, sarcomere formation, and active tension generation. All serum‐free media examined were capable of inducing myotube formation and the expression of muscle‐specific proteins. All serum‐free media except for F‐12 gave the sarcomere structure. Active tension generation was observed for cells that differentiated in AIM and Ult‐G, but the active tension generated by C2C12 cells that differentiated in Ult‐G was only ∼25% in the case of myotubes that formed in HS. The addition of Ult‐G to the AIM resulted in improvement of the active tension generation capability, the active tension generated being ∼3.4× compared to that in HS. The approach for assessing muscle cell differentiation presented in this study will be suitable for other studies that involve the differentiation of muscle cells. Biotechnol. Bioeng. 2010;107: 894-901.</description><subject>AIM-V</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>C2C12</subject><subject>Cell Differentiation</subject><subject>Cells</subject><subject>Culture Media - chemistry</subject><subject>Culture Media, Serum-Free</subject><subject>Differentiation</subject><subject>F-12</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene expression</subject><subject>Glucose</subject><subject>Ham</subject><subject>Health. Pharmaceutical industry</subject><subject>Industrial applications and implications. Economical aspects</subject><subject>Media</subject><subject>Metabolism</subject><subject>Mice</subject><subject>Miscellaneous</subject><subject>muscle</subject><subject>Muscle Fibers, Skeletal - physiology</subject><subject>Muscle Tonus</subject><subject>Muscles</subject><subject>Muscular system</subject><subject>Myoblasts - physiology</subject><subject>Proteins</subject><subject>serum-free</subject><subject>Serums</subject><subject>Ultroser-G</subject><issn>0006-3592</issn><issn>1097-0290</issn><issn>1097-0290</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkd9qFDEUxoModl298AV0EES9mPYk2fyZS13rWiiVYouX4Uw2U1JnJ2syU9078Ql8Rp_ErLOtIKgQyDnkd75zTj5CHlLYpwDsoPb9PmNailtkQqFSJbAKbpMJAMiSi4rtkXspXeZUaSnvkj0Gkgsu2IR8O7zCdsDeh64ITZFcHFY_vn5vonPF0jeNi67r_fhuQ7f02ygVTYjFnM0pK1abULeY-sK6tk0FpuTyWeag6EOBtvdXruhdl7YKF65zcSeGa6x96_vNfXKnwTa5B7t7Ss7fHJ7N35bH7xZH85fHpRVqJspK4JKicFrXitVKIFhbKdQMASpHHaKskarKajurG9FowJpXNXfIGMvFfEqejbrrGD4NLvVm5dN2auxcGJLRWkMlgcv_kkoC40woncnn_ySpVFSAZJRn9Mkf6GUYYpc3NkpUcqbVbJahFyNkY0gpusaso19h3BgKZuu1yV6bX15n9tFOcKhXbnlDXpubgac7AJPFtonYWZ9-c5xrDnnhKTkYuc--dZu_dzSvjs6uW5djhU-9-3JTgfGjkYorYT6cLMwJP-ULuTg1rzP_eOQbDAYvYp7i_D0DyoFWwPMn8Z9ew9nZ</recordid><startdate>20101201</startdate><enddate>20101201</enddate><creator>Fujita, Hideaki</creator><creator>Endo, Akiko</creator><creator>Shimizu, Kazunori</creator><creator>Nagamori, Eiji</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><general>Wiley Subscription Services, Inc</general><scope>FBQ</scope><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7T7</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20101201</creationdate><title>Evaluation of serum‐free differentiation conditions for C2C12 myoblast cells assessed as to active tension generation capability</title><author>Fujita, Hideaki ; Endo, Akiko ; Shimizu, Kazunori ; Nagamori, Eiji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5745-95ad1a5e88b72b75a0cc97a82a009e1eaa6ba179c8c4bf5f80ab39b3ea22295a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>AIM-V</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>C2C12</topic><topic>Cell Differentiation</topic><topic>Cells</topic><topic>Culture Media - chemistry</topic><topic>Culture Media, Serum-Free</topic><topic>Differentiation</topic><topic>F-12</topic><topic>Fundamental and applied biological sciences. 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Bioeng</addtitle><date>2010-12-01</date><risdate>2010</risdate><volume>107</volume><issue>5</issue><spage>894</spage><epage>901</epage><pages>894-901</pages><issn>0006-3592</issn><issn>1097-0290</issn><eissn>1097-0290</eissn><coden>BIBIAU</coden><abstract>We have compared several serum‐free media for the differentiation of C2C12 myoblasts and assessed the extent of differentiation in several ways including as to active tension generation capability. C2C12 cells were allowed to differentiate in Dulbecco's modified Eagle's medium (DMEM) containing Ham's F‐12 (F‐12), AIM‐V (AIM), 0.2% Ultroser‐G in DMEM (Ult‐G), and 0.1% Sericin in DMEM (Sericin), compared with in DMEM supplemented with 2% horse serum (HS) or 2% calf serum (CS). C2C12 differentiation was assessed as the extent of myotube formation, glucose metabolism, protein expression, sarcomere formation, and active tension generation. All serum‐free media examined were capable of inducing myotube formation and the expression of muscle‐specific proteins. All serum‐free media except for F‐12 gave the sarcomere structure. Active tension generation was observed for cells that differentiated in AIM and Ult‐G, but the active tension generated by C2C12 cells that differentiated in Ult‐G was only ∼25% in the case of myotubes that formed in HS. The addition of Ult‐G to the AIM resulted in improvement of the active tension generation capability, the active tension generated being ∼3.4× compared to that in HS. The approach for assessing muscle cell differentiation presented in this study will be suitable for other studies that involve the differentiation of muscle cells. Biotechnol. Bioeng. 2010;107: 894-901.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>20635352</pmid><doi>10.1002/bit.22865</doi><tpages>8</tpages></addata></record> |
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| subjects | AIM-V Animals Biological and medical sciences Biotechnology C2C12 Cell Differentiation Cells Culture Media - chemistry Culture Media, Serum-Free Differentiation F-12 Fundamental and applied biological sciences. Psychology Gene expression Glucose Ham Health. Pharmaceutical industry Industrial applications and implications. Economical aspects Media Metabolism Mice Miscellaneous muscle Muscle Fibers, Skeletal - physiology Muscle Tonus Muscles Muscular system Myoblasts - physiology Proteins serum-free Serums Ultroser-G |
| title | Evaluation of serum‐free differentiation conditions for C2C12 myoblast cells assessed as to active tension generation capability |
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