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首页> 外文期刊>The international journal of biochemistry and cell biology >Acute exposure of L6 myotubes to cis-9, trans-11 and trans-10, cis-12 conjugated linoleic acid isomers stimulates glucose uptake by modulating Ca 2+/calmodulin-dependent protein kinase II
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Acute exposure of L6 myotubes to cis-9, trans-11 and trans-10, cis-12 conjugated linoleic acid isomers stimulates glucose uptake by modulating Ca 2+/calmodulin-dependent protein kinase II

机译:L6肌管对顺式9,反式11和反式10,顺式12的亚油酸异构体的急性暴露通过调节Ca 2 + /钙调蛋白依赖性蛋白激酶II刺激葡萄糖摄取。

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摘要

Conjugated linoleic acid (CLA), a dietary fat, has been considered beneficial in metabolic syndrome. Despite several findings indicating that CLA improves glucose clearance, little information is available regarding the cellular dynamics of CLA on skeletal muscle. We sought to investigate the role of Ca 2+/calmodulin-dependent protein kinase II (CaMKII) in cis-9, trans-11(c9,t11) and trans-10, cis-12 (t10,c12) CLA isomer-mediated glucose transport by L6 myotubes. t10,c12-CLA stimulated both intracellular Ca 2+ release (Ca i 2+) and CaMKII phosphorylation, whereas c9,t11-CLA showed only modest effects on both. Sequestering Ca i 2+ with BAPTA/AM abrogated the effect of both CLA isomers on Akt substrate-160 kDa (AS160) phosphorylation and glucose uptake by myotubes. Exposing myotubes to KN-93 or autocamtide 2-related inhibitory peptide to block CaMKII activity prevented both CLA isomers from inducing AS160 phosphorylation and glucose transport. Likewise, genetic knockdown of CaMKII in myotubes using siRNA completely abolished CLA isomer-mediated glucose uptake. These results indicate that CLA isomers require Ca i 2+-CaMKII to mediate glucose uptake. Evidence that CaMKII blockers inhibit t10,c12-CLA-mediated AMP-activated protein kinase (AMPK) activation indicated that CaMKII acts upstream of AMPK in response to t10,c12-CLA. Lastly, CLA isomers stimulated the formation of reactive oxygen species but had no effect on stress-activated protein kinase/c-jun NH 2-terminal kinase. These data establish that t10,c12-CLA acts via Ca i 2+-CaMKII-AMPK-AS160 to stimulate skeletal muscle glucose transport, whereas the mechanism of c9,t11-CLA remains unclear. Given that impairments in muscle glucose utilisation are apparent in metabolic syndrome, delineating the molecular mechanisms by which CLA isomers mediate muscle glucose uptake may identify new approaches to manage this condition.
机译:膳食脂肪共轭亚油酸(CLA)被认为对代谢综合症有益。尽管有一些发现表明CLA可改善葡萄糖清除率,但有关CLA在骨骼肌上的细胞动力学的信息很少。我们试图研究Ca 2 + /钙调蛋白依赖性蛋白激酶II(CaMKII)在CLA异构体介导的cis-9,trans-11(c9,t11)和trans-10,cis-12(t10,c12)中的作用L6肌管传输葡萄糖。 t10,c12-CLA刺激细胞内Ca 2+释放(Ca i 2+)和CaMKII磷酸化,而c9,t11-CLA仅对两者具有适度的作用。用BAPTA / AM螯合Ca 2+消除了两种CLA异构体对Akt底物160 kDa(AS160)磷酸化和肌管摄取葡萄糖的影响。将肌管暴露于KN-93或与自身肽2相关的抑制肽以阻断CaMKII活性,可防止CLA异构体诱导AS160磷酸化和葡萄糖转运。同样,使用siRNA进行肌管中CaMKII的基因敲除完全消除了CLA异构体介导的葡萄糖摄取。这些结果表明CLA异构体需要Ca 2+ -CaMKII来介导葡萄糖摄取。 CaMKII阻滞剂抑制t10,c12-CLA介导的AMP激活的蛋白激酶(AMPK)激活的证据表明,CaMKII响应t10,c12-CLA在AMPK的上游起作用。最后,CLA异构体刺激了活性氧的形成,但对应力激活的蛋白激酶/ c-jun NH 2末端激酶没有影响。这些数据表明,t10,c12-CLA通过Ca 2 + -CaMKII-AMPK-AS160刺激骨骼肌葡萄糖转运,而c9,t11-CLA的机制尚不清楚。鉴于肌肉糖利用的损害在代谢综合症中很明显,描述CLA异构体介导肌肉葡萄糖摄取的分子机制可能会找到新的方法来管理这种情况。

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