内质网
未折叠蛋白反应
细胞生物学
细胞器
免疫印迹
组蛋白脱乙酰酶抑制剂
化学
组蛋白脱乙酰基酶
癌症研究
生物
组蛋白
生物化学
基因
作者
Melisa Halilovic,Lisa Marx-Blümel,Christian Marx,Katrin Buder,James F. Beck,Jürgen Sonnemann
标识
DOI:10.1007/978-1-0716-2788-4_17
摘要
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.
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