Department of Life Sciences, Graduate School of Arts and Sciences, The University of Tokyo, 3-8-1 Komaba, Meguro-ku, Tokyo, Japan.
Mol Cell Biochem. 2011 Jan;347(1-2):145-55. doi: 10.1007/s11010-010-0622-3. Epub 2010 Oct 19.
We investigated the spatial and temporal expression patterns of hypoxia-inducible factor-1α (HIF-1α) during muscle regeneration and myogenesis in a C2C12 cell culture system. The expression of HIF-1α synchronized with that of myogenic regulatory genes during muscle regeneration at both the mRNA and protein levels. The HIF-1α protein was localized in the nuclei of newly formed regenerating myofibers in three different muscle injury models, including freezing, bupivacaine injection, and muscular dystrophy. In myogenic cell culture, the HIF-1α protein was localized in the nucleus and cytoplasm of the majority of myoblasts and myotubes. HIF-1α protein expression decreased concomitant with the increased expression of MyoD and myogenin proteins after the induction of myogenic differentiation. We investigated the adaptive response of myoblasts to hypoxia-like conditions induced by treatment of cobalt chloride. This treatment allowed HIF-1α to accumulate and translocate to the nucleus to activate transcription of its target genes, suggesting that myoblasts adapted to acute hypoxia-like conditions through enhancing an HIF-1-dependent pathway. Our results provide insight into the possible involvement of HIF-1α in myogenesis in vivo and in vitro.
我们研究了缺氧诱导因子-1α(HIF-1α)在 C2C12 细胞培养系统中的肌肉再生和肌发生过程中的时空表达模式。HIF-1α 的表达在肌肉再生过程中与肌生成调节基因的表达在 mRNA 和蛋白质水平上同步。HIF-1α 蛋白在三种不同的肌肉损伤模型(包括冷冻、布比卡因注射和肌肉营养不良)中,在新形成的再生肌纤维的细胞核中定位。在肌发生细胞培养中,HIF-1α 蛋白定位于大多数成肌细胞和肌管的细胞核和细胞质中。HIF-1α 蛋白表达随着肌生成分化诱导后 MyoD 和 myogenin 蛋白表达的增加而降低。我们研究了肌母细胞对钴氯化物诱导的类似缺氧条件的适应性反应。这种处理允许 HIF-1α 积累并转移到细胞核中,激活其靶基因的转录,表明肌母细胞通过增强 HIF-1 依赖性途径来适应急性类似缺氧的条件。我们的结果提供了对 HIF-1α 在体内和体外肌发生中可能参与的深入了解。