Literature DB >> 25804745

Assays for induction of the unfolded protein response and selective activation of the three major pathways.

Ananya Gupta1, Danielle E Read, Sanjeev Gupta.   

Abstract

The endoplasmic reticulum (ER) is responsible for the proper folding and processing of secreted and transmembrane proteins within the cell. Stimuli that disrupt ER function cause an accumulation of misfolded proteins within the ER lumen, a condition termed ER stress. The unfolded protein response (UPR) is activated in response to ER stress in an attempt to restore ER homeostasis. UPR is initiated by three transmembrane sensors that activate three signaling pathways which lead to the activation of transcription factors and production of chaperones. The coordinated action of these three pathways attempt to restore homeostasis. However, if the ER homeostasis cannot be restored, it initiates apoptosis. Deregulated or compromised functions of these pathways can therefore lead to the pathogenesis of disease. In order to understand the molecular mechanisms involved, it is important to study each pathway independently. Here, we describe a number of approaches to selectively target each arm of UPR and investigate the functional significance of the UPR pathway involved.

Mesh:

Year:  2015        PMID: 25804745     DOI: 10.1007/978-1-4939-2522-3_2

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  8 in total

1.  Age-related dysfunction of the autophago-lysosomal pathway in human endothelial cells.

Authors:  Sören Mai; Nadine Brehm; Georg Auburger; Jürgen Bereiter-Hahn; Marina Jendrach
Journal:  Pflugers Arch       Date:  2019-06-21       Impact factor: 3.657

Review 2.  Liver function and dysfunction - a unique window into the physiological reach of ER stress and the unfolded protein response.

Authors:  D Thomas Rutkowski
Journal:  FEBS J       Date:  2018-02-07       Impact factor: 5.542

3.  Tanshinone IIA ameliorates apoptosis of cardiomyocytes induced by endoplasmic reticulum stress.

Authors:  Jun Feng; Shusheng Li; Huawen Chen
Journal:  Exp Biol Med (Maywood)       Date:  2016-07-28

4.  NCOA3 coactivator is a transcriptional target of XBP1 and regulates PERK-eIF2α-ATF4 signalling in breast cancer.

Authors:  A Gupta; M M Hossain; N Miller; M Kerin; G Callagy; S Gupta
Journal:  Oncogene       Date:  2016-04-25       Impact factor: 9.867

5.  Clofoctol and sorafenib inhibit prostate cancer growth via synergistic induction of endoplasmic reticulum stress and UPR pathways.

Authors:  Lixia Fan; Zhenglei He; Sarah A Head; Yinghui Zhou; Ting Lu; Xulong Feng; Xueqing Zhang; Meng Zhang; Yongjun Dang; Xinghong Jiang; Minghua Wang
Journal:  Cancer Manag Res       Date:  2018-10-23       Impact factor: 3.989

6.  Downregulation of miR-17-92 Cluster by PERK Fine-Tunes Unfolded Protein Response Mediated Apoptosis.

Authors:  Danielle E Read; Ananya Gupta; Karen Cawley; Laura Fontana; Patrizia Agostinis; Afshin Samali; Sanjeev Gupta
Journal:  Life (Basel)       Date:  2021-01-06

7.  Hyperglycemia-triggered ATF6-CHOP pathway aggravates acute inflammatory liver injury by β-catenin signaling.

Authors:  Chao Yang; Zeng Wang; Yuanchang Hu; Shikun Yang; Feng Cheng; Jianhua Rao; Xuehao Wang
Journal:  Cell Death Discov       Date:  2022-03-14

8.  PERK regulated miR-424(322)-503 cluster fine-tunes activation of IRE1 and ATF6 during Unfolded Protein Response.

Authors:  Ananya Gupta; Muhammad Mosaraf Hossain; Danielle E Read; Claudio Hetz; Afshin Samali; Sanjeev Gupta
Journal:  Sci Rep       Date:  2015-12-17       Impact factor: 4.379

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.