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重组腺相关病毒载体激活细胞未折叠蛋白反应。

Activation of the cellular unfolded protein response by recombinant adeno-associated virus vectors.

机构信息

Department of Hematology, Christian Medical College, Vellore, Tamil Nadu, India.

出版信息

PLoS One. 2013;8(1):e53845. doi: 10.1371/journal.pone.0053845. Epub 2013 Jan 8.

Abstract

The unfolded protein response (UPR) is a stress-induced cyto-protective mechanism elicited towards an influx of large amount of proteins in the endoplasmic reticulum (ER). In the present study, we evaluated if AAV manipulates the UPR pathways during its infection. We first examined the role of the three major UPR axes, namely, endoribonuclease inositol-requiring enzyme-1 (IRE1α), activating transcription factor 6 (ATF6) and PKR-like ER kinase (PERK) in AAV infected cells. Total RNA from mock or AAV infected HeLa cells were used to determine the levels of 8 different ER-stress responsive transcripts from these pathways. We observed a significant up-regulation of IRE1α (up to 11 fold) and PERK (up to 8 fold) genes 12-48 hours after infection with self-complementary (sc)AAV2 but less prominent with single-stranded (ss)AAV2 vectors. Further studies demonstrated that scAAV1 and scAAV6 also induce cellular UPR in vitro, with AAV1 vectors activating the PERK pathway (3 fold) while AAV6 vectors induced a significant increase on all the three major UPR pathways [6-16 fold]. These data suggest that the type and strength of UPR activation is dependent on the viral capsid. We then examined if transient inhibition of UPR pathways by RNA interference has an effect on AAV transduction. siRNA mediated silencing of PERK and IRE1α had a modest effect on AAV2 and AAV6 mediated gene expression (∼1.5-2 fold) in vitro. Furthermore, hepatic gene transfer of scAAV2 vectors in vivo, strongly elevated IRE1α and PERK pathways (2 and 3.5 fold, respectively). However, when animals were pre-treated with a pharmacological UPR inhibitor (metformin) during scAAV2 gene transfer, the UPR signalling and its subsequent inflammatory response was attenuated concomitant to a modest 2.8 fold increase in transgene expression. Collectively, these data suggest that AAV vectors activate the cellular UPR pathways and their selective inhibition may be beneficial during AAV mediated gene transfer.

摘要

未折叠蛋白反应(UPR)是一种内质网(ER)中大量蛋白质流入时引发的应激诱导的细胞保护机制。在本研究中,我们评估了腺相关病毒(AAV)在感染过程中是否会改变 UPR 途径。我们首先检查了三条主要 UPR 轴的作用,即内切核酸酶肌醇需求酶 1(IRE1α)、激活转录因子 6(ATF6)和蛋白激酶 R 样内质网激酶(PERK)在 AAV 感染细胞中的作用。用 mock 或 AAV 感染的 HeLa 细胞的总 RNA 来确定这些途径中 8 种不同的 ER 应激反应转录本的水平。我们观察到自互补(sc)AAV2 感染 12-48 小时后,IRE1α(高达 11 倍)和 PERK(高达 8 倍)基因显著上调,但单链(ss)AAV2 载体的上调不明显。进一步的研究表明,scAAV1 和 scAAV6 也在体外诱导细胞 UPR,AAV1 载体激活 PERK 途径(3 倍),而 AAV6 载体诱导所有三条主要 UPR 途径显著增加[6-16 倍]。这些数据表明,UPR 激活的类型和强度取决于病毒衣壳。然后,我们检查了 UPR 途径的瞬时抑制是否会影响 AAV 转导。体外 PERK 和 IRE1α 的 siRNA 介导沉默对 AAV2 和 AAV6 介导的基因表达有适度影响(约 1.5-2 倍)。此外,体内 scAAV2 载体的肝基因转移强烈上调 IRE1α 和 PERK 途径(分别为 2 倍和 3.5 倍)。然而,当动物在 scAAV2 基因转移期间用药理学 UPR 抑制剂(二甲双胍)预处理时,UPR 信号及其随后的炎症反应减弱,同时转基因表达适度增加 2.8 倍。总的来说,这些数据表明 AAV 载体激活细胞 UPR 途径,其选择性抑制可能在 AAV 介导的基因转移过程中有益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6921/3540029/d8201371f9b4/pone.0053845.g001.jpg

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