Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5501998 | Free Radical Biology and Medicine | 2017 | 39 Pages |
Abstract
IsoLGs represent a newly identified class of activators of HSC in vitro, which are biologically active at concentrations as low as 500 pM, and are particularly effective at promoting a pro-inflammatory response and autophagy.
Keywords
XBP1GAPDHICAM-1NF-kBERKSfMqRT-PCRDAPIHBSSMTS5-bromo-2-deoxyuridineUPRIL8PARPIL6TIMP-1LC3Bp38MAPKCOL1A1Collagen type I alpha 1carboxy-H2DCFDAIsolevuglandinsisolevuglandinPDIα-SMAJnk4-HNECCL2ATF42′,7′-dichlorodihydrofluorescein diacetate4′,6-diamidino-2-phenylindole4-hydroxy-2-nonenalBiPc-Jun N-terminal kinaseIL1βROSalpha smooth muscle actinAutophagyEndoplasmic reticulum stressinflammationLOXInterleukin-8interleukin-6Interleukin-1 betaBrdUanalysis of varianceANOVAEnzyme-linked immunosorbent assayELISAOxidative stressCHOPstandard error of the meanquantitative reverse transcription PCRserum free mediumendoplasmic reticulumnuclear factor kappa Bactivating transcription factor 4Fibrosislactate dehydrogenaseLDHLysyl oxidaseHank's balanced salt solutionSEMintracellular adhesion moleculeUnfolded protein responseX-box binding protein 1Immunoglobulin heavy chain binding proteinprotein disulfide isomeraseCCAAT-enhancer-binding protein homologous proteinp38 mitogen-activated protein kinasespoly (ADP-ribose) polymerasecomplete mediumChloroquinechemokine (C-C motif) ligand 2glyceraldehyde 3-phosphate dehydrogenaseReactive oxygen species
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Authors
Lisa Longato, Fausto Andreola, Sean S. Davies, Jackson L. Roberts, Giuseppe Fusai, Massimo Pinzani, Kevin Moore, Krista Rombouts,