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评估组蛋白去乙酰化酶抑制剂诱导的内质网应激。

Assessment of HDAC Inhibitor-Induced Endoplasmic Reticulum (ER) Stress.

机构信息

Leibniz Institute on Aging - Fritz Lipmann Institute (FLI), Jena, Germany.

Department of Pediatric Hematology and Oncology, Children's Clinic, Jena University Hospital, Jena, Germany.

出版信息

Methods Mol Biol. 2023;2589:253-268. doi: 10.1007/978-1-0716-2788-4_17.

Abstract

The endoplasmic reticulum (ER) is a multifunctional cell organelle which is important for the folding and processing of proteins. Different endogenous and exogenous factors can disturb the ER homeostasis, causing ER stress and activating the unfolded protein response (UPR) to remove misfolded proteins and aggregates. ER stress and the UPR are associated with several human diseases, such as diabetes, Alzheimer's or Parkinson's disease, and cancer. Histone deacetylase inhibitors (HDACi) are used to treat cancer and were shown to induce ER stress/to modulate the UPR, although the exact mechanism is not fully understood and needs further research. Several approaches to monitoring ER stress exist. Here we describe methods including qPCR, Western blot, transmission electron microscopy, and fluorescence microscopy to analyze changes in mRNA and protein expression levels as well as defects in ER structures after HDAC inhibitor-induced ER stress.

摘要

内质网(ER)是一种多功能的细胞器,对于蛋白质的折叠和加工非常重要。不同的内源性和外源性因素可以干扰 ER 稳态,导致 ER 应激并激活未折叠蛋白反应(UPR),以去除错误折叠的蛋白质和聚集体。ER 应激和 UPR 与几种人类疾病有关,如糖尿病、阿尔茨海默病或帕金森病和癌症。组蛋白去乙酰化酶抑制剂(HDACi)用于治疗癌症,并被证明能诱导 ER 应激/调节 UPR,尽管确切的机制尚不完全清楚,需要进一步研究。有几种监测 ER 应激的方法。在这里,我们描述了一些方法,包括 qPCR、Western blot、透射电子显微镜和荧光显微镜,以分析 HDAC 抑制剂诱导的 ER 应激后 mRNA 和蛋白质表达水平的变化以及 ER 结构的缺陷。

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