Polynomial algebra reveals diverging roles of the unfolded protein response in endothelial cells during ischemia-reperfusion injury

被引:7
|
作者
Le Pape, Sylvain [1 ]
Dimitrova, Elena [2 ]
Hannaert, Patrick [1 ]
Konovalov, Alexander [3 ]
Volmer, Romain [4 ,5 ]
Ron, David [4 ,5 ]
Thuillier, Raphael [1 ]
Hauet, Thierry [1 ]
机构
[1] Univ Med & Pharm Poitiers, INSERM, IRTOMIT, UMR 1082, F-86021 Poitiers, France
[2] Clemson Univ, Clemson, SC 29634 USA
[3] Univ St Andrews, Ctr Interdisciplinary Res Computat Algebra, Sch Comp Sci, St Andrews KY16 9SX, Fife, Scotland
[4] Univ Cambridge, Metab Res Labs, Cambridge CB2 0QQ, England
[5] Cambridge Biomed Res Ctr, Natl Inst Hlth Res, Cambridge CB2 0QQ, England
来源
FEBS LETTERS | 2014年 / 588卷 / 17期
基金
英国工程与自然科学研究理事会; 英国惠康基金;
关键词
Ischemia-reperfusion injury (IRI); Unfolded protein response (UPR); Endothelial cells (EC); Murine embryonic cells (MEC); Probabilistic polynomial dynamical systems (PDS); Gene regulatory networks (GRN); ENDOPLASMIC-RETICULUM STRESS; KIDNEY-TRANSPLANTATION; ER-STRESS; DEATH; APOPTOSIS; NETWORKS; ACTIVATION; DISEASE; MODELS; DONORS;
D O I
10.1016/j.febslet.2014.05.065
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The unfolded protein response (UPR) - the endoplasmic reticulum stress response - is found in various pathologies including ischemia-reperfusion injury (IRI). However, its role during IRI is still unclear. Here, by combining two different bioinformatical methods - a method based on ordinary differential equations (Time Series Network Inference) and an algebraic method (probabilistic polynomial dynamical systems) - we identified the IRE1 alpha-XBP1 and the ATF6 pathways as the main UPR effectors involved in cell's adaptation to IRI. We validated these findings experimentally by assessing the impact of their knock-out and knock-down on cell survival during IRI. (C) 2014 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:3062 / 3067
页数:6
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