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首页> 外文期刊>Journal of cell biology >Generation of a stable, posttranslationally modified microtubule array is an early event in myogenic differentiation.
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Generation of a stable, posttranslationally modified microtubule array is an early event in myogenic differentiation.

机译:稳定的,翻译后修饰的微管阵列的产生是成肌分化的早期事件。

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Microtubules (MTs) have been implicated to function in the change of cell shape and intracellular organization that occurs during myogenesis. However, the mechanism by which MTs are involved in these morphogenetic events is unclear. As a first step in elucidating the role of MTs in myogenesis, we have examined the accumulation and subcellular distribution of posttranslationally modified forms of tubulin in differentiating rat L6 muscle cells, using antibodies specific for tyrosinated (Tyr), detyrosinated (Glu), and acetylated (Ac) tubulin. Both Glu and Ac tubulin are components of stable MTs, whereas Tyr tubulin is the predominant constituent of dynamic MTs. In proliferating L6 myoblasts, as in other types of proliferating cells, the level of Glu tubulin was very low when compared with the level of Tyr tubulin. However, when we shifted proliferating L6 cells to differentiation media, we observed a rapid accumulation of Glu tubulin in cellular MTs. By immunofluorescence, the increase in Glu tubulin was first detected in MTs of prefusion myoblasts and was specifically localized to MTs that were associated with elongating portions of the cell. MTs in the multinucleated myotubes observed at later stages of differentiation maintained the elevated level of Glu tubulin that was observed in the prefusion myoblasts. When cells at early stages of differentiation (less than 1 d after switching the culture medium) were immunostained for Glu tubulin and the muscle-specific marker, muscle myosin, we found that the increase in Glu tubulin preceded the accumulation of muscle myosin. Thus, the elaboration of Glu MTs is one of the very early events in myogenesis. Ac tubulin also increased during L6 myogenesis; however, the increase in acetylation occurred later in myogenesis, after fusion had already occurred. Because detyrosination was temporally correlated with early events of myogenesis, we examined the mechanism responsible for the accumulation of Glu tubulin in the MTs of prefusion myoblasts. We found that an increase in the stability of L6 cell MTs occurred at the onset of differentiation, suggesting that the early increase in detyrosination that we observed is a manifestation of a decrease in MT dynamics in elongating myoblasts. We conclude that the establishment of an oriented array of microtubules heightened in its stability and its level of posttranslationally modified subunits may be involved in the subcellular remodeling that occurs during myogenesis.
机译:微管(MTs)已牵涉到在成肌过程中发生的细胞形状和细胞内组织变化中起作用。但是,尚不清楚MTs参与这些形态发生事件的机制。作为阐明MT在肌发生中作用的第一步,我们使用酪氨酸(Tyr),脱酪氨酸(Glu)和乙酰化抗体,研究了微管蛋白翻译后修饰形式在大鼠L6肌肉细胞中的积累和亚细胞分布。 (Ac)微管蛋白。 Glu和Ac微管蛋白都是稳定MT的成分,而Tyr微管蛋白是动态MT的主要成分。与其他类型的增殖细胞一样,在增殖的L6成肌细胞中,与酪氨酸微管蛋白的水平相比,Glu微管蛋白的水平非常低。但是,当我们将增殖的L6细胞转移至分化培养基时,我们观察到了Glu微管蛋白在细胞MT中的快速积累。通过免疫荧光法,首先在融合前成肌细胞的MT中检测到Glu微管蛋白的增加,并特异性地定位于与细胞伸长部分相关的MT。在分化后期观察到的多核肌管中的MT保持了在融合前成肌细胞中观察到的Glu微管蛋白水平的升高。当在分化的早期阶段(切换培养基后少于1 d)对Glu微管蛋白和肌肉特异性标记肌肌球蛋白进行免疫染色时,我们发现Glu微管蛋白的增加先于肌肉肌球蛋白的积累。因此,Glu MTs的形成是肌发生中非常早期的事件之一。 Ac微管蛋白在L6肌发生过程中也增加;但是,乙酰化的增加发生在融合发生后的肌生成后期。因为脱酪氨酸在时间上与肌发生的早期事件相关,所以我们检查了导致预混成肌细胞MT中Glu微管蛋白积累的机制。我们发现,L6细胞MT的稳定性增加是在分化开始时发生的,这表明我们观察到的脱酪氨酸的早期增加是延长成肌细胞中MT动态降低的表现。我们得出的结论是,定向的微管阵列的建立在其稳定性和其翻译后修饰的亚基水平上提高了,可能参与了在成肌过程中发生的亚细胞重塑。

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