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A Helical Polypeptide‐Based Potassium Ionophore Induces Endoplasmic Reticulum Stress‐Mediated Apoptosis by Perturbing Ion Homeostasis

机译:一种基于螺旋多肽的钾离子载体通过干扰离子稳态来诱导内质网应激介导的细胞凋亡。

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摘要

Perturbation of potassium homeostasis can affect various cell functions and lead to the onset of programmed cell death. Although ionophores have been intensively used as an ion homeostasis disturber, the mechanisms of cell death are unclear and the bioapplicability is limited. In this study, helical polypeptide‐based potassium ionophores are developed to induce endoplasmic reticulum (ER) stress‐mediated apoptosis. The polypeptide‐based potassium ionophores disturb ion homeostasis and then induce prolonged ER stress in the cells. The ER stress results in oxidative environments that accelerate the activation of mitochondria‐dependent apoptosis. Moreover, ER stress‐mediated apoptosis is triggered in a tumor‐bearing mouse model that suppresses tumor proliferation. This study provides the first evidence showing that helical polypeptide‐based potassium ionophores trigger ER stress‐mediated apoptosis by perturbation of potassium homeostasis.
机译:钾稳态的扰动会影响各种细胞功能,并导致程序性细胞死亡的发作。尽管离子载体已被广泛用作离子稳态干扰物,但细胞死亡的机制尚不清楚,并且生物适用性受到限制。在这项研究中,开发了基于螺旋多肽的钾离子载体,以诱导内质网(ER)应激介导的细胞凋亡。基于多肽的钾离子载体干扰离子稳态,然后在细胞中诱导延长的内质网应激。 ER应力导致氧化环境加速线粒体依赖性细胞凋亡的激活。此外,内质网应激介导的细胞凋亡在荷瘤小鼠模型中被触发,从而抑制了肿瘤的扩散。这项研究提供了第一个证据,表明基于螺旋多肽的钾离子载体通过扰动钾稳态来触发内质网应激介导的细胞凋亡。

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