Barjot C, Cotten M L, Goblet C, Whalen R G, Bacou F
Laboratoire de Différenciation Cellulaire et Croissance, Institut National de la Recherche Agronomique, Montpellier, France.
J Muscle Res Cell Motil. 1995 Dec;16(6):619-28. doi: 10.1007/BF00130243.
We investigated the myogenic properties of rabbit fast or slow muscle satellite cells during their differentiation in culture, with a particular attention to the expression of myosin heavy chain and myogenic regulatory factor genes. Satellite cells were isolated from Semimembranosus proprius (slow-twitch muscle; 100% type I fibres) and Semimembranosus accessorius (fast-twitch muscle; almost 100% type II fibres) muscles of 3-month-old rabbits. Satellite cells in culture possess different behaviours according to their origin. Cells isolated from slow muscle proliferate faster, fuse earlier into more numerous myotubes and mature more rapidly into striated contractile fibres than do cells isolated from fast muscle. This pattern of proliferation and differentiation is also seen in the expression of myogenic regulatory factor genes. Myf5 is detected in both fast or slow 6-day-old cell cultures, when satellite cells are in the exponential stage of proliferation. MyoD and myogenin are subsequently detected in slow satellite cell cultures, but their expression in fast cell cultures is delayed by 2 and 4 days respectively. MRF4 is detected in both types of cultures when they contain striated and contractile myofibres. Muscle-specific myosin heavy chains are expressed earlier in slow satellite cell cultures. No adult myosin heavy chain isoforms are detected in fast cell cultures for 13 days, whereas cultures from slow cells express neonatal, adult slow and adult fast myosin heavy chain isoforms at that time. In both fast and slow satellite cell cultures containing striated contractile fibres, neonatal and adult myosin heavy chain isoforms are coexpressed. However, cultures made from satellite cells derived from slow muscles express the slow myosin heavy chain isoform, in addition to the neonatal and the fast isoforms. These results are further supported by the expression of the mRNA encoding the adult myosin heavy chain isoforms. These data provide further evidence for the existence of satellite cell diversity between two rabbit muscles of different fibre-type composition, and also suggest the existence of differently preprogrammed satellite cells.
我们研究了兔快肌或慢肌卫星细胞在体外培养分化过程中的肌源性特性,特别关注肌球蛋白重链和肌源性调节因子基因的表达。卫星细胞取自3月龄兔的半膜肌固有部(慢肌;100%为I型纤维)和副半膜肌(快肌;几乎100%为II型纤维)。培养中的卫星细胞根据其来源表现出不同的行为。与从快肌分离的细胞相比,从慢肌分离的细胞增殖更快,更早融合形成更多的肌管,并更快成熟为横纹收缩纤维。这种增殖和分化模式在肌源性调节因子基因的表达中也可见。在快肌或慢肌来源的6日龄细胞培养物中均检测到Myf5,此时卫星细胞处于增殖指数期。随后在慢肌卫星细胞培养物中检测到MyoD和肌细胞生成素,但它们在快肌细胞培养物中的表达分别延迟2天和4天。当两种培养物中含有横纹收缩肌纤维时均检测到MRF4。肌肉特异性肌球蛋白重链在慢肌卫星细胞培养物中表达更早。在快肌细胞培养物中13天内未检测到成年肌球蛋白重链异构体,而此时慢肌细胞培养物已表达新生型、成年慢型和成年快型肌球蛋白重链异构体。在含有横纹收缩纤维的快肌和慢肌卫星细胞培养物中,新生型和成年型肌球蛋白重链异构体均共表达。然而,由慢肌来源的卫星细胞制成的培养物除了表达新生型和快型异构体外,还表达慢型肌球蛋白重链异构体。编码成年肌球蛋白重链异构体的mRNA的表达进一步支持了这些结果。这些数据为不同纤维类型组成的两种兔肌肉之间存在卫星细胞多样性提供了进一步证据,也提示存在预先编程不同的卫星细胞。