Stary Creed M, Hogan Michael C
Department of Medicine, University of California, San Diego, La Jolla, California; and Department of Anesthesiology, Perioperative and Pain Medicine, Stanford University School of Medicine, Stanford, California
Department of Medicine, University of California, San Diego, La Jolla, California; and.
J Appl Physiol (1985). 2016 May 15;120(10):1260-6. doi: 10.1152/japplphysiol.01060.2015. Epub 2016 Feb 11.
The intrinsic activating factors that induce transcription of heat shock protein 72 (HSP72) in skeletal muscle following exercise remain unclear. We hypothesized that the cytosolic Ca(2+) transient that occurs with depolarization is a determinant. We utilized intact, single skeletal muscle fibers from Xenopus laevis to test the role of the cytosolic Ca(2+) transient and several other exercise-related factors (fatigue, hypoxia, AMP kinase, and cross-bridge cycling) on the activation of HSP72 transcription. HSP72 and HSP60 mRNA levels were assessed with real-time quantitative PCR; cytosolic Ca(2+) concentration ([Ca(2+)]cyt) was assessed with fura-2. Both fatiguing and nonfatiguing contractions resulted in a significant increase in HSP72 mRNA. As expected, peak [Ca(2+)]cyt remained tightly coupled with peak developed tension in contracting fibers. Pretreatment with N-benzyl-p-toluene sulfonamide (BTS) resulted in depressed peak developed tension with stimulation, while peak [Ca(2+)]cyt remained largely unchanged from control values. Despite excitation-contraction uncoupling, BTS-treated fibers displayed a significant increase in HSP72 mRNA. Treatment of fibers with hypoxia (Po2: <3 mmHg) or AMP kinase activation had no effect on HSP72 mRNA levels. These results suggest that the intermittent cytosolic Ca(2+) transient that occurs with skeletal muscle depolarization provides a sufficient activating stimulus for HSP72 transcription. Metabolic or mechanical factors associated with fatigue development and cross-bridge cycling likely play a more limited role.
运动后诱导骨骼肌中热休克蛋白72(HSP72)转录的内在激活因子仍不清楚。我们假设去极化时发生的胞质Ca(2+)瞬变是一个决定因素。我们利用非洲爪蟾完整的单根骨骼肌纤维来测试胞质Ca(2+)瞬变以及其他几个与运动相关的因素(疲劳、缺氧、AMP激酶和横桥循环)对HSP72转录激活的作用。通过实时定量PCR评估HSP72和HSP60 mRNA水平;用fura-2评估胞质Ca(2+)浓度([Ca(2+)]cyt)。疲劳性和非疲劳性收缩均导致HSP72 mRNA显著增加。正如预期的那样,收缩纤维中[Ca(2+)]cyt峰值与峰值张力仍紧密相关。用N-苄基对甲苯磺酰胺(BTS)预处理会导致刺激时峰值张力降低,而[Ca(2+)]cyt峰值与对照值相比基本保持不变。尽管兴奋-收缩解偶联,但BTS处理的纤维中HSP72 mRNA仍显著增加。用缺氧(Po2:<3 mmHg)处理纤维或激活AMP激酶对HSP72 mRNA水平没有影响。这些结果表明,骨骼肌去极化时发生的间歇性胞质Ca(2+)瞬变为HSP72转录提供了足够的激活刺激。与疲劳发展和横桥循环相关的代谢或机械因素可能起的作用更有限。