Redox cell signaling and hepatic progenitor cells

European Journal of Cell Biology(2018)

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摘要
Hepatic diseases are widespread in the world and organ transplantation is currently the only treatment for liver failure. New cell-based approaches have been considered, since stem cells may represent a possible source to treat liver diseases. Acute and chronic liver diseases are characterized by high production of reactive oxygen and nitrogen species, with consequent oxidative modifications of cellular macromolecules and alteration of signaling pathways, metabolism and cell cycle. Although considered harmful molecules, reactive species are involved in cell growth and differentiation processes, modulating the activity of transcription factors, which take part in stemness/proliferation. It is conceivable that redox balance may regulate the development of hepatic progenitor cells, function and survival in synchrony with metabolism during chronic liver diseases. This review aims to summarize diverse redox-sensitive signaling pathways involved in stem cell fate, highlighting the important role of hepatic progenitor cells as a possible source to treat end-stage liver disease for organ regeneration.
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NAFLD,ROS,RNS,ETC,TCA,SODs,CAT,GSH,GPX,OMM,VDAC,GSSG,Grx,Trx,Δψ,PTP,FoxO,NRF2,PRDM16,TRP53,Nrx,AREs,Keap1,GSK–3β,Dv1,Nrx,NOX1,p38-MAPK,APE/REF1,PTEN,IGF-1,mTOR,PGC-1α,EGF,PDGF,PTP1b,CDC25,JNK1,ATM,NLRP3,ERK1/2,FAK,TRF,ISCs,PI3K,MEF2C,PIKE,SRF,HIF,HSCs,NSCs,MSCs,HBV,HCV,MDA,ALD,NASH,CYP2E1,I/R,AIH,PBC,PSC,HCC,DILI,hiPSCs,hESCs,HPCs,FGF7,HGF/c.MET
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