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营养剥夺和溶酶体应激诱导视网膜色素上皮细胞中 TFEB 的激活。

Nutrient deprivation and lysosomal stress induce activation of TFEB in retinal pigment epithelial cells.

机构信息

1School of Optometry, Indiana University, Bloomington, IN 47405 USA.

2State University of New York College of Optometry, 33 42nd St., New York, NY 10036 USA.

出版信息

Cell Mol Biol Lett. 2019 May 27;24:33. doi: 10.1186/s11658-019-0159-8. eCollection 2019.

Abstract

BACKGROUND

Induction of lysosomal function and autophagy is regarded as an adaptive mechanism in response to cellular stress. The transcription factor EB (TFEB) has been identified as a master regulator of lysosomal function and autophagy. TFEB is a member of the microphthalmia family of bHLH-LZ transcription factors that includes other members such as micropthalmia-associated transcription factor (MITF), TFE3, and TFEC. TFEB controls lysosome biogenesis and autophagy by upregulation of a family of genes belonging to the Coordinated Lysosomal Expression and Regulation (CLEAR) network. Here, we investigated the expression of TFEB in cells subjected to nutrient deprivation and lysosomal stress. We studied transcriptional induction of TFEB-regulated genes in response to nutrient deprivation and lysosomal stress in retinal pigment epithelial (RPE) cells. Furthermore, we also investigated the induction of autophagy and lysosomal genes upon overexpression of constitutively active form of TFEB.

METHODS

Expression of TFEB and MITF protein levels were evaluated in cells subjected to prolonged periods of nutrient deprivation. mRNA levels of the CLEAR network genes was measured by quantitative real time PCR (qRT-PCR) analysis in cells deprived of nutrients, treated with ammonium chloride and upon overexpression of constitutively active TFEB. Immunostaining with LC3 antibody was used to measure autophagy flux. Labeling with lysoTracker dye was used to assess lysosomes.

RESULTS

Our results show that nutrient deprivation increases protein levels of TFEB and MITF in ARPE-19 cells. Nutrient stress induces the expression of lysosomal (LAMP1, CTSD MCOLN1, SGSH) and autophagy (BECN1) genes. Lysosomal stress also increases the expression of lysosomal (ATP6V0A1 and LAMP1) and autophagy (p62 and BECN1) genes. Our results show that overexpression of constitutively active TFEB also induces the expression of CLEAR network genes.

CONCLUSIONS

Collectively, these observations suggest that nutrient stress induces the protein expression of both MITF and TFEB in ARPE-19 cells. TFEB-regulated transcriptional program plays an important role in adaptive response of cells during both nutrient and lysosomal stress.

摘要

背景

溶酶体功能和自噬的诱导被认为是细胞应激的一种适应机制。转录因子 EB(TFEB)已被确定为溶酶体功能和自噬的主要调节因子。TFEB 是微phthalmia 家族 bHLH-LZ 转录因子的成员,其他成员包括小眼相关转录因子(MITF)、TFE3 和 TFEC。TFEB 通过上调属于协调溶酶体表达和调节(CLEAR)网络的基因家族来控制溶酶体生物发生和自噬。在这里,我们研究了营养剥夺和溶酶体应激下细胞中 TFEB 的表达。我们研究了营养剥夺和溶酶体应激下视网膜色素上皮(RPE)细胞中 TFEB 调节基因的转录诱导。此外,我们还研究了过表达组成型激活形式的 TFEB 时自噬和溶酶体基因的诱导。

方法

评估了在经历长时间营养剥夺的细胞中 TFEB 和 MITF 蛋白水平的表达。通过定量实时 PCR(qRT-PCR)分析测量了缺乏营养、用氯化铵处理和过表达组成型激活 TFEB 时 CLEAR 网络基因的 mRNA 水平。用 LC3 抗体进行免疫染色来测量自噬通量。用溶酶体染料标记来评估溶酶体。

结果

我们的结果表明,营养剥夺会增加 ARPE-19 细胞中 TFEB 和 MITF 的蛋白水平。营养应激诱导溶酶体(LAMP1、CTSD、MCOLN1、SGSH)和自噬(BECN1)基因的表达。溶酶体应激也增加了溶酶体(ATP6V0A1 和 LAMP1)和自噬(p62 和 BECN1)基因的表达。我们的结果表明,过表达组成型激活的 TFEB 也会诱导 CLEAR 网络基因的表达。

结论

综上所述,这些观察结果表明,营养应激会诱导 ARPE-19 细胞中 MITF 和 TFEB 的蛋白表达。TFEB 调节的转录程序在细胞营养和溶酶体应激期间的适应性反应中起着重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf5b/6537441/b525d8c6e934/11658_2019_159_Fig1_HTML.jpg

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