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首页> 外文期刊>Journal of Biophysical and Biochemical Cytology >Srf controls satellite cell fusion through the maintenance of actin architecture
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Srf controls satellite cell fusion through the maintenance of actin architecture

机译:SRF通过维护Actin架构来控制卫星电池融合

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摘要

Satellite cells (SCs) are adult muscle stem cells that are mobilized when muscle homeostasis is perturbed. Here, we show that serum response factor (Srf) is needed for optimal SC-mediated hypertrophic growth. We identified Srf as a master regulator of SC fusion required in both fusion partners, whereas it was dispensable for SC proliferation and differentiation. We show that SC-specific Srf deletion leads to impaired actin cytoskeleton and report the existence of finger-like actin–based protrusions at fusion sites in vertebrates that were notoriously absent in fusion-defective myoblasts lacking Srf. Restoration of a polymerized actin network by overexpression of an α-actin isoform in Srf mutant SCs rescued their fusion with a control cell in vitro and in vivo and reestablished overload-induced muscle growth. These findings demonstrate the importance of Srf in controlling the organization of actin cytoskeleton and actin-based protrusions for myoblast fusion in mammals and its requirement to achieve efficient hypertrophic myofiber growth.
机译:卫星细胞(SCS)是当肌肉稳态扰动时动员的成年肌肉干细胞。在这里,我们表明最佳SC介导的肥厚生长需要血清响应因子(SRF)。我们将SRF作为融合伙伴中所需的SC融合的主稳压器确定,而SC扩散和分化是可分配的。我们表明SC特异性SRF缺失导致肌动蛋白细胞骨架损害,并报告存在于脊椎动物的融合位点的指状肌动蛋白的突起,缺乏SRF的融合型肌细胞令人缺乏。通过在SRF突变体SC中过表达通过过表达恢复聚合的肌动蛋白网络SCS在体外和体内拯救与对照细胞的融合,并重新建立过载引起的肌肉生长。这些研究结果证明了SRF在控制肌动蛋白细胞骨架和肌动蛋白的突起中用于哺乳动物中的肌细胞融合的组织的重要性及其要求实现有效的肥厚性肌无力的增长。

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