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Insulin/IGF-1 and ROS signaling pathway cross-talk in aging and longevity determination.

机译:胰岛素/ IGF-1和ROS信号通路在衰老和寿命确定中相互影响。

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摘要

Regulation of hormonal, insulin/IGF-1 (Ins/IGF-1) signaling activities, and pathways of the intrinsic generation of reactive oxygen species (ROS) play a role in aging and longevity determination. In this review we discuss the cross-talk between these pathways as mechanisms of signaling that may be important factors in the regulation of aging and longevity. The balance of physiological processes controlling the rate of aging and longevity in several mouse mutants suggests the involvement of cross-talk mechanisms of regulation of the insulin/IGF1 signaling pathway vs. the ROS signaling pathways. In mice, modulation of the Ins/IGF-1 signaling pathways resulting from the Prop1(df), Pit1(dw) and Igf1 receptor mutations exemplify the hormonal pathways associated with aging and longevity determination. These pathways are also targets of the ROS-mediated redox pathways. Similarly, the Klotho and p66(Shc) mutants link regulation of ROS signaling pathways to aging and longevity determination. Both of these models also display altered insulin signaling activity, a characteristic associated with longevity. The Ins/IGF-1 signaling pathway is of particular interest because of its decreased activity due to genetic manipulation vs. its responsiveness to ROS levels.
机译:激素,胰岛素/ IGF-1(Ins / IGF-1)信号传导活动的调节以及活性氧(ROS)内在生成的途径在衰老和寿命确定中发挥作用。在这篇综述中,我们将这些途径之间的相互影响作为信号传导机制进行讨论,这可能是调节衰老和长寿的重要因素。在几个小鼠突变体中,控制衰老和长寿率的生理过程之间的平衡表明,涉及胰岛素/ IGF1信号通路与ROS信号通路调节的串扰机制。在小鼠中,由Prop1(df),Pit1(dw)和Igf1受体突变引起的Ins / IGF-1信号通路的调节是与衰老和长寿相关的激素途径的例证。这些途径也是ROS介导的氧化还原途径的靶标。同样,Klotho和p66(Shc)突变体将ROS信号通路的调控与衰老和寿命确定联系起来。这两个模型还显示出改变的胰岛素信号传导活性,这是与寿命相关的特征。 Ins / IGF-1信号传导途径特别受关注,因为其因基因操作而降低的活性与其对ROS水平的响应能力有关。

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