Department of Biomolecular Sciences, University of Urbino Carlo Bo, Urbino, Italy.
Exp Cell Res. 2010 Jul 15;316(12):1977-84. doi: 10.1016/j.yexcr.2010.04.006. Epub 2010 Apr 24.
Micro-vesicles can be released by different cell types and operate as 'safe containers' mediating inter-cellular communication. In this work we investigated whether cultured myoblasts could release exosomes. The reported data demonstrate, for the first time, that C2C12 myoblasts release micro-vesicles as shown by the presence of two exosome markers (Tsg101 and Alix proteins). Using real-time PCR analysis it was shown that these micro-vesicles, like other cell types, carry mtDNA. Proteomic characterization of the released micro-vesicle contents showed the presence of many proteins involved in signal transduction. The bioinformatics assessment of the Disorder Index and Aggregation Index of these proteins suggested that C2C12 micro-vesicles mainly deliver the machinery for signal transduction to target cells rather than key proteins involved in hub functions in molecular networks. The presence of IGFBP-5 in the purified micro-vesicles represents an exception, since this binding protein can play a key role in the modulation of the IGF-1 signalling pathway. In conclusion, the present findings demonstrate that skeletal muscle cells release micro-vesicles, which probably have an important role in the communication processes within skeletal muscles and between skeletal muscles and other organs. In particular, the present findings suggest possible new diagnostic approaches to skeletal muscle diseases.
微泡可以由不同的细胞类型释放,并作为介导细胞间通讯的“安全容器”发挥作用。在这项工作中,我们研究了培养的成肌细胞是否可以释放外泌体。报告的数据首次表明,C2C12 成肌细胞释放微泡,如两个外泌体标记物(Tsg101 和 Alix 蛋白)的存在所示。使用实时 PCR 分析表明,这些微泡与其他细胞类型一样,携带 mtDNA。释放的微泡内容物的蛋白质组学特征表明存在许多参与信号转导的蛋白质。这些蛋白质的无序指数和聚集指数的生物信息学评估表明,C2C12 微泡主要向靶细胞输送信号转导的机制,而不是参与分子网络中枢纽功能的关键蛋白质。纯化的微泡中 IGFBP-5 的存在是一个例外,因为这种结合蛋白可以在 IGF-1 信号通路的调节中发挥关键作用。总之,本研究结果表明,骨骼肌细胞释放微泡,这可能在骨骼肌内和骨骼肌与其他器官之间的通讯过程中发挥重要作用。特别是,本研究结果提示了针对骨骼肌疾病的可能新的诊断方法。