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内质网伴侣蛋白 calnexin 控制线粒体定位和呼吸。

The ER chaperone calnexin controls mitochondrial positioning and respiration.

机构信息

Faculty of Medicine and Dentistry, Department of Cell Biology, University of Alberta, Edmonton, Alberta T6G 2H7, Canada.

Complex Systems Research Center, Shanxi University, Taiyuan 030006, China.

出版信息

Sci Signal. 2020 Jun 30;13(638):eaax6660. doi: 10.1126/scisignal.aax6660.

Abstract

Chaperones in the endoplasmic reticulum (ER) control the flux of Ca ions into mitochondria, thereby increasing or decreasing the energetic output of the oxidative phosphorylation pathway. An example is the abundant ER lectin calnexin, which interacts with sarco/endoplasmic reticulum Ca ATPase (SERCA). We found that calnexin stimulated the ATPase activity of SERCA by maintaining its redox state. This function enabled calnexin to control how much ER Ca was available for mitochondria, a key determinant for mitochondrial bioenergetics. Calnexin-deficient cells compensated for the loss of this function by partially shifting energy generation to the glycolytic pathway. These cells also showed closer apposition between the ER and mitochondria. Calnexin therefore controls the cellular energy balance between oxidative phosphorylation and glycolysis.

摘要

内质网(ER)中的伴侣蛋白控制钙离子流入线粒体的流量,从而增加或减少氧化磷酸化途径的能量输出。一个例子是丰富的 ER 凝集素 calnexin,它与肌浆/内质网 Ca ATP 酶(SERCA)相互作用。我们发现 calnexin 通过维持其氧化还原状态来刺激 SERCA 的 ATP 酶活性。这个功能使 calnexin 能够控制 ER 中可供线粒体使用的 Ca 量,这是线粒体生物能学的关键决定因素。缺乏 calnexin 的细胞通过部分转向糖酵解途径来补偿这种功能的丧失。这些细胞还显示 ER 和线粒体之间更接近的毗邻。因此,calnexin 控制着氧化磷酸化和糖酵解之间的细胞能量平衡。

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