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诱导自噬和激活蛋白酶体平衡可减少蛋白毒性细胞死亡:一种恢复光感受器内稳态的新型治疗方法。

Shifting the balance of autophagy and proteasome activation reduces proteotoxic cell death: a novel therapeutic approach for restoring photoreceptor homeostasis.

机构信息

Department of Ophthalmology and Visual Sciences, University of Michigan Medical School, Kellogg Eye Center, Ann Arbor, MI, USA.

Department of Ophthalmology, Xiangya School of medicine, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.

出版信息

Cell Death Dis. 2019 Jul 18;10(8):547. doi: 10.1038/s41419-019-1780-1.

Abstract

The P23H variant of rhodopsin results in misfolding of the protein, and is a common cause of the blinding disease autosomal dominant retinitis pigmentosa (adRP). We have recently demonstrated that degeneration of photoreceptor cells in retinas of P23H mice is due to the endoplasmic reticulum stress (ERS)-induced activation of autophagy that leads to a secondary proteasome insufficiency and activation of cell death pathways. We propose that this increased level of autophagy flux relative to proteasome activity, which we term the A:P ratio, represents a marker of altered photoreceptor cell homeostasis, and that therapies aimed at normalizing this ratio will result in increased photoreceptor cell survival. To test this postulate, we treated P23H mice with a chemical chaperone (4-phenylbutyric acid) to improve rhodopsin folding, or with a selective phosphodiesterase-4 inhibitor (rolipram) to increase proteasome activity. P23H mice treated with either of these agents exhibited reduced ERS, decreased autophagy flux, increased proteasome activity, and decreased activation of cell death pathways. In addition, rates of retinal degeneration were decreased, and photoreceptor morphology and visual function were preserved. These findings support the conclusion that normalizing the A:P ratio, either by reducing the ERS-induced activation of autophagy, or by increasing proteasome activity, improves photoreceptor survival, and suggest a potential new therapeutic strategy for the treatment of adRP caused by protein folding defects.

摘要

P23H 视蛋白变体导致蛋白质错误折叠,是常染色体显性遗传视网膜色素变性(adRP)这种致盲疾病的一个常见病因。我们最近的研究表明,P23H 小鼠视网膜中感光细胞的退化是由于内质网应激(ERS)诱导的自噬激活,导致次级蛋白酶体不足和细胞死亡途径的激活。我们提出,与蛋白酶体活性相比,自噬通量的这种增加水平,我们称之为 A:P 比值,代表了光感受器细胞内稳态改变的标志物,而旨在使该比值正常化的治疗方法将导致光感受器细胞存活增加。为了验证这一假设,我们用化学伴侣(4-苯丁酸)治疗 P23H 小鼠以改善视蛋白折叠,或用选择性磷酸二酯酶-4 抑制剂(罗利普兰)增加蛋白酶体活性。用这两种药物中的任何一种治疗的 P23H 小鼠均表现出 ERS 减少、自噬通量减少、蛋白酶体活性增加和细胞死亡途径激活减少。此外,视网膜退化的速度降低,光感受器形态和视觉功能得到保留。这些发现支持了这样的结论,即通过减少 ERS 诱导的自噬激活或增加蛋白酶体活性来使 A:P 比值正常化,可以改善光感受器的存活,并为治疗由蛋白质折叠缺陷引起的 adRP 提供了一种新的潜在治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d63e/6639359/b79a1aab973b/41419_2019_1780_Fig1_HTML.jpg

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