A novel in vitro three-dimensional skeletal muscle model

被引:21
|
作者
Marquette, Michele L. [1 ]
Byerly, Diane
Sognier, Marguerite
机构
[1] Univ Texas, Med Branch, Dept Neurosci & Cell Biol, Galveston, TX 77550 USA
[2] NASA, Lyndon B Johnson Space Ctr, Div Human Adaptat & Countermeasures, Houston, TX 77058 USA
[3] Univ Space Res Assoc, Div Space Life Sci, Houston, TX USA
基金
美国国家航空航天局;
关键词
C2C12; cells; muscle; differentiation; three-dimensional; rotary cell culture system;
D O I
10.1007/s11626-007-9054-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A novel three-dimensional (3D) skeletal muscle model composed of C2C12 mouse myoblasts is described. This model was generated by cultivating myoblasts in suspension using the rotary cell culture system (RCCS), a unique culture environment. Single-cell suspensions of myoblasts were seeded at 5x10(5)/ml in growth medium without exogenous support structures or substrates. Cell aggregation occurred in both RCCS and suspension control (SC) conditions within 12 h but occurred more rapidly in the SC at all time intervals examined. RCCS-cultured myoblasts fused and differentiated into a 3D construct without serum deprivation or alterations. Syncitia were quantified at 3 and 6+ d in stained thin sections. A significantly greater number of syncitia was found at 6+ d in the RCCS cultures compared to the SC. The majority of syncitia were localized to the periphery of the cell constructs for all treatments. The expression of sarcomeric myosin heavy chain (MHC) was localized at or near the periphery of the 3D construct. The majority of MHC was associated with the large cells (syncitia) of the 6+-d aggregates. These results show, for the first time, that myoblasts form syncitia and express MHC in the presence of growth factors and without the use of exogenous supports or substrates. This model test system is useful for investigating initial cell binding, myoblast fusion and syncitia formation, and differentiation processes.
引用
收藏
页码:255 / 263
页数:9
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