Institute of Pathophysiology, Faculty of Medicine, University of Ljubljana, Zaloška 4, Ljubljana, 1000, Slovenia.
J Muscle Res Cell Motil. 2024 Sep;45(3):155-169. doi: 10.1007/s10974-024-09679-3. Epub 2024 Jul 31.
Pyruvate dehydrogenase kinase (PDK), which phosphorylates the pyruvate dehydrogenase complex, regulates glucose metabolism in skeletal muscle. PDK1, an isozyme whose expression is controlled by hypoxia-inducible factor-1α (HIF-1α), is thought to play a role in muscle adaptation to hypoxia. While transcriptional upregulation of PDK1 by HIF-1α is well characterised, mechanisms controlling proteolysis of PDK1 in skeletal muscle have not been thoroughly investigated. Proteasome inhibitor MG132 paradoxically reduced the abundance of PDK1 in human cancer cells and rat L6 myotubes, suggesting that MG132 might direct PDK1 towards autophagic degradation. The objectives of our current study were to determine (1) whether MG132 suppresses PDK1 levels in primary human myotubes, (2) whether chloroquine, an inhibitor of autophagy, prevents MG132-induced suppression of PDK1 in L6 myotubes, and (3) whether PYR-41, an inhibitor of ubiquitination, suppresses PDK1 in L6 myotubes. Using qPCR and/or immunoblotting, we found that despite markedly upregulating HIF-1α protein, MG132 did not alter the PDK1 expression in cultured primary human myotubes, while it suppressed both PDK1 mRNA and protein in L6 myotubes. The PDK1 levels in L6 myotubes were suppressed also during co-treatment with chloroquine and MG132. PYR-41 markedly increased the abundance of HIF-1α in primary human and L6 myotubes, while reducing the abundance of PDK1. In L6 myotubes treated with PYR-41, chloroquine increased the abundance of the epidermal growth factor receptor, but did not prevent the suppression of PDK1. Collectively, our results suggest that cultured myotubes degrade PDK1 via a pathway that cannot be inhibited by MG132, PYR-41, and/or chloroquine.
丙酮酸脱氢酶激酶(PDK)可使丙酮酸脱氢酶复合物磷酸化,从而调节骨骼肌中的葡萄糖代谢。PDK1 是一种同工酶,其表达受缺氧诱导因子-1α(HIF-1α)调控,被认为在肌肉对缺氧的适应中发挥作用。虽然 HIF-1α 对 PDK1 的转录上调已有很好的描述,但控制骨骼肌中 PDK1 蛋白水解的机制尚未得到彻底研究。蛋白酶体抑制剂 MG132 出人意料地降低了人癌细胞和大鼠 L6 肌管中的 PDK1 丰度,这表明 MG132 可能将 PDK1 定向到自噬降解。我们目前研究的目的是确定:(1)MG132 是否抑制原代人肌管中的 PDK1 水平;(2)氯喹,一种自噬抑制剂,是否能阻止 MG132 诱导的 L6 肌管中 PDK1 的抑制;(3)PYR-41,一种泛素化抑制剂,是否抑制 L6 肌管中的 PDK1。使用 qPCR 和/或免疫印迹,我们发现,尽管 MG132 明显上调了 HIF-1α 蛋白,但并未改变培养的原代人肌管中的 PDK1 表达,同时也抑制了 L6 肌管中的 PDK1 mRNA 和蛋白。在 L6 肌管中,氯喹和 MG132 共同处理也抑制了 PDK1 水平。PYR-41 显著增加了原代人肌管和 L6 肌管中 HIF-1α 的丰度,同时降低了 PDK1 的丰度。在 L6 肌管中用 PYR-41 处理后,氯喹增加了表皮生长因子受体的丰度,但不能阻止 PDK1 的抑制。总之,我们的结果表明,培养的肌管通过一种不能被 MG132、PYR-41 和/或氯喹抑制的途径降解 PDK1。