Differential sensitivity of metabolically competent and non-competent HepaRG cells to apoptosis induced by diclofenac combined or not with TNF-alphaReportar como inadecuado




Differential sensitivity of metabolically competent and non-competent HepaRG cells to apoptosis induced by diclofenac combined or not with TNF-alpha - Descarga este documento en PDF. Documentación en PDF para descargar gratis. Disponible también para leer online.

* Corresponding author 1 Lebanese University Beirut 2 Foie, métabolismes et cancer 3 CHU Pontchaillou Rennes 4 ImPACcell - Plate-forme ImPACcell

Abstract : The role of reactive metabolites and inflammatory stress has been largely evoked in idiosyncratic hepatotoxicity of diclofenac DCF; however mechanisms remain poorly understood. We aimed to evaluate the influence of liver cell phenotype on the hepatotoxicity of DCF combined or not with TNF-alpha using differentiated and undifferentiated HepaRG cells, and for comparison, HepG2 cells. Our results demonstrate that after a 24 h-treatment metabolizing HepaRG cells were less sensitive to DCF than their undifferentiated non-metabolizing counterparts as shown by lower oxidative and endoplasmic reticulum stress responses and lower activation of caspase 9. Differentiated HepaRG cells were also less sensitive than HepG2 cells. Their lower sensitivity to DCF was related to their high content in glutathione transferases. DCF-induced apoptotic effects were potentiated by TNF-alpha only in death receptor-expressing differentiated HepaRG and HepG2 cells and were associated with marked activation of caspase 8. TNF-alpha co-treatment did not aggravate DCF-induced cholestatic features. Altogether, our results demonstrate that i lower sensitivity to DCF of differentiated HepaRG cells compared to their non-metabolically active counterparts was related to their high detoxifying capacity, giving support to the higher sensitivity of nonhepatic tissues than liver to this drug; ii TNF-alpha-potentiation of DCF cytotoxicity occurred only in death receptor-expressing cells.

Keywords : toxicity stress hepatotoxicity expression primary human hepatocytes acyl glucuronide rat hepatocytes liver-injury in-vitro activation





Autor: Houssein Al-Attrache - Ahmad Sharanek - Audrey Burban - Matthew Burbank - Thomas Gicquel - Ziad Abdel-Razzak - Christiane Guguen-

Fuente: https://hal.archives-ouvertes.fr/



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