Dzeja Petras P, Terzic Andre, Wieringa Bé
Department of Biochemistry, University of Minnesota, Minneapolis, MN, USA.
Mol Cell Biochem. 2004 Jan-Feb;256-257(1-2):13-27. doi: 10.1023/b:mcbi.0000009856.23646.38.
To assess the significance of energy supply routes in cellular energetic homeostasis, net phosphoryl fluxes catalyzed by creatine kinase (CK), adenylate kinase (AK) and glycolytic enzymes were quantified using 18O-phosphoryl labeling. Diaphragm muscle from double M-CK/ScCKmit knockout mice exhibited virtually no CK-catalyzed phosphotransfer. Deletion of the cytosolic M-CK reduced CK-catalyzed phosphotransfer by 20%, while the absence of the mitochondrial ScCKmit isoform did not affect creatine phosphate metabolic flux. Contribution of the AK-catalyzed phosphotransfer to total cellular ATP turnover was 15.0, 17.2, 20.2 and 28.0% in wild type, ScCKmit, M-CK and M-CK/ScCKmit deficient muscles, respectively. Glycolytic phosphotransfer, assessed by G-6-P 18O-phosphoryl labeling, was elevated by 32 and 65% in M-CK and M-CK/ScCKmit deficient muscles, respectively. Inhibition of glyceraldehyde 3-phosphate dehydrogenase (GAPDH)/phosphoglycerate kinase (PGK) in CK deficient muscles abolished inorganic phosphate compartmentation and redirected high-energy phosphoryl flux through the AK network. Under such conditions, AK phosphotransfer rate was equal to 86% of the total cellular ATP turnover concomitant with almost normal muscle performance. This indicates that near-equilibrium glycolytic phosphotransfer reactions catalyzed by the GAPDH/PGK support a significant portion of the high-energy phosphoryl transfer in CK deficient muscles. However, CK deficient muscles displayed aberrant ATPase-ATPsynthase communication along with lower energetic efficiency (P/O ratio), and were more sensitive to metabolic stress induced by chemical hypoxia. Thus, redistribution of phosphotransfer through glycolytic and AK networks contributes to energetic homeostasis in muscles under genetic and metabolic stress complementing loss of CK function.
为评估能量供应途径在细胞能量稳态中的重要性,利用18O-磷酰标记对肌酸激酶(CK)、腺苷酸激酶(AK)和糖酵解酶催化的净磷酰通量进行了定量分析。来自双M-CK/ScCKmit基因敲除小鼠的膈肌几乎没有CK催化的磷酰转移。胞质M-CK的缺失使CK催化的磷酰转移减少了20%,而线粒体ScCKmit同工型的缺失并不影响磷酸肌酸的代谢通量。在野生型、ScCKmit、M-CK和M-CK/ScCKmit缺陷型肌肉中,AK催化的磷酰转移对细胞总ATP周转的贡献分别为15.0%、17.2%、20.2%和28.0%。通过G-6-P 18O-磷酰标记评估的糖酵解磷酰转移在M-CK和M-CK/ScCKmit缺陷型肌肉中分别升高了32%和65%。在CK缺陷型肌肉中抑制甘油醛3-磷酸脱氢酶(GAPDH)/磷酸甘油酸激酶(PGK)消除了无机磷酸的区室化,并使高能磷酰通量通过AK网络重新定向。在这种情况下,AK磷酰转移速率等于细胞总ATP周转的86%,同时肌肉性能几乎正常。这表明由GAPDH/PGK催化的近平衡糖酵解磷酰转移反应支持了CK缺陷型肌肉中很大一部分高能磷酰转移。然而,CK缺陷型肌肉显示出异常的ATP酶-ATP合酶通讯以及较低的能量效率(P/O比),并且对化学性缺氧诱导的代谢应激更敏感。因此,通过糖酵解和AK网络的磷酰转移重新分布有助于在遗传和代谢应激下肌肉中的能量稳态,补充CK功能的丧失。