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Myotube formation on micro-patterned glass: Intracellular organization and protein distribution in C2C12 skeletal muscle cells
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2008 (English)In: Journal of Histochemistry and Cytochemistry, ISSN 0022-1554, E-ISSN 1551-5044, Vol. 56, no 10, 881-892 p.Article in journal (Refereed) Published
Abstract [en]

Proliferation and fusion of myoblasts are needed for the generation and repair of multinucleated skeletal muscle fibers in vivo. Studies of myocyte differentiation, cell fusion, and muscle repair are limited by an appropriate in vitro muscle cell culture system. We developed a novel cell culture technique [two-dimensional muscle syncytia (2DMS) technique] that results in formation of myotubes, organized in parallel much like the arrangement in muscle tissue. This technique is based on UV lithography-produced micro-patterned glass on which conventionally cultured C2C12 myoblasts proliferate, align, and fuse to neatly arranged contractile myotubes in parallel arrays. Combining this technique with fluorescent microscopy, we observed alignment of actin filament bundles and a perinuclear distribution of glucose transporter 4 after myotube formation. Newly formed myotubes contained adjacently located MyoD-positive and MyoD-negative nuclei, suggesting fusion of MyoD-positive and MyoD-negative cells. In comparison, the closely related myogenic factor Myf5 did not exhibit this pattern of distribution. Furthermore, cytoplasmic patches of MyoD colocalized with bundles of filamentous actin near myotube nuclei. At later stages of differentiation, all nuclei in the myotubes were MyoD negative. The 2DMS system is thus a useful tool for studies on muscle alignment, differentiation, fusion, and subcellular protein localization.

Place, publisher, year, edition, pages
2008. Vol. 56, no 10, 881-892 p.
Keyword [en]
skeletal muscle in vitro culturing, MyoD, glucose transporter 4, F-actin, myogenesis, cell fusion, differentiation
National Category
Cell Biology Engineering and Technology
URN: urn:nbn:se:uu:diva-107885DOI: 10.1369/jhc.2008.951228ISI: 000259515500002OAI: oai:DiVA.org:uu-107885DiVA: diva2:233430
Available from: 2009-09-01 Created: 2009-08-31 Last updated: 2016-04-13Bibliographically approved

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