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Endoplasmic reticulum stress does not contribute to steatohepatitis in obese and insulin-resistant high-fat-diet-fed foz/foz mice.

Bibliographic reference Legry, Vanessa ; Van Rooyen, Derrick M ; Lambert, Barbara ; Sempoux, Christine ; Poekes, Laurence ; et. al. Endoplasmic reticulum stress does not contribute to steatohepatitis in obese and insulin-resistant high-fat-diet-fed foz/foz mice.. In: Clinical Science, Vol. 127, no. 7, p. 507-518 (2014)
Permanent URL http://hdl.handle.net/2078.1/146242
  1. Leclercq Isabelle A., Emerging Concepts on the Pathogenesis of Non-Alcoholic Steatohepatitis (NASH), Non-Alcoholic Fatty Liver Disease ISBN:9781118556153 p.46-61, 10.1002/9781118556153.ch5
  2. Tilg Herbert, Moschen Alexander R., Evolution of inflammation in nonalcoholic fatty liver disease: The multiple parallel hits hypothesis, 10.1002/hep.24001
  3. Ron David, Walter Peter, Signal integration in the endoplasmic reticulum unfolded protein response, 10.1038/nrm2199
  4. Hendershot L, Mt. Sinai J. Med., 71, 289 (2004)
  5. Dara Lily, Ji Cheng, Kaplowitz Neil, The contribution of endoplasmic reticulum stress to liver diseases, 10.1002/hep.24279
  6. Scheuner Donalyn, Song Benbo, McEwen Edward, Liu Chuan, Laybutt Ross, Gillespie Patrick, Saunders Thom, Bonner-Weir Susan, Kaufman Randal J, Translational Control Is Required for the Unfolded Protein Response and In Vivo Glucose Homeostasis, 10.1016/s1097-2765(01)00265-9
  7. Kammoun Hélène L., Chabanon Hervé, Hainault Isabelle, Luquet Serge, Magnan Christophe, Koike Tatsuro, Ferré Pascal, Foufelle Fabienne, GRP78 expression inhibits insulin and ER stress–induced SREBP-1c activation and reduces hepatic steatosis in mice, 10.1172/jci37007
  8. Ozcan U., Endoplasmic Reticulum Stress Links Obesity, Insulin Action, and Type 2 Diabetes, 10.1126/science.1103160
  9. Yang Jae-Seong, Kim Jin Taek, Jeon Jouhyun, Park Ho Sun, Kang Gyeong Hoon, Park Kyong Soo, Lee Hong Kyu, Kim Sanguk, Cho Young Min, Changes in Hepatic Gene Expression upon Oral Administration of Taurine-Conjugated Ursodeoxycholic Acid in ob/ob Mice, 10.1371/journal.pone.0013858
  10. Puri Puneet, Mirshahi Faridoddin, Cheung Onpan, Natarajan Ramesh, Maher James W., Kellum John M., Sanyal Arun J., Activation and Dysregulation of the Unfolded Protein Response in Nonalcoholic Fatty Liver Disease, 10.1053/j.gastro.2007.10.039
  11. Gregor M. F., Yang L., Fabbrini E., Mohammed B. S., Eagon J. C., Hotamisligil G. S., Klein S., Endoplasmic Reticulum Stress Is Reduced in Tissues of Obese Subjects After Weight Loss, 10.2337/db08-1220
  12. Kumashiro N., Erion D. M., Zhang D., Kahn M., Beddow S. A., Chu X., Still C. D., Gerhard G. S., Han X., Dziura J., Petersen K. F., Samuel V. T., Shulman G. I., Cellular mechanism of insulin resistance in nonalcoholic fatty liver disease, 10.1073/pnas.1113359108
  13. Heydet Déborah, Chen Lesley X., Larter Claire Z., Inglis Chrystal, Silverman Michael A., Farrell Geoffrey C., Leroux Michel R., A truncating mutation of Alms1 reduces the number of hypothalamic neuronal cilia in obese mice, 10.1002/dneu.22031
  14. Arsov Todor, Silva Diego G., O’Bryan Moira K., Sainsbury Amanda, Lee Nicola J., Kennedy Claire, Manji Shehnaaz S.M., Nelms Keats, Liu Conan, Vinuesa Carola G., de Kretser David M., Goodnow Christopher C., Petrovsky Nikolai, Fat Aussie—A New Alström Syndrome Mouse Showing a Critical Role for ALMS1 in Obesity, Diabetes, and Spermatogenesis, 10.1210/me.2005-0494
  15. Arsov Todor, Larter Claire Z., Nolan Christopher J., Petrovsky Nikolai, Goodnow Christopher C., Teoh Narcissus C., Yeh Matthew M., Farrell Geoffrey C., Adaptive failure to high-fat diet characterizes steatohepatitis in Alms1 mutant mice, 10.1016/j.bbrc.2006.02.032
  16. Schaap Frank G., Kremer Andreas E., Lamers Wouter H., Jansen Peter L.M., Gaemers Ingrid C., Fibroblast growth factor 21 is induced by endoplasmic reticulum stress, 10.1016/j.biochi.2012.10.019
  17. Liang B., Wang S., Wang Q., Zhang W., Viollet B., Zhu Y., Zou M.-H., Aberrant Endoplasmic Reticulum Stress in Vascular Smooth Muscle Increases Vascular Contractility and Blood Pressure in Mice Deficient of AMP-Activated Protein Kinase- 2 In Vivo, 10.1161/atvbaha.112.300606
  18. Lanthier N., Molendi-Coste O., Cani P. D., van Rooijen N., Horsmans Y., Leclercq I. A., Kupffer cell depletion prevents but has no therapeutic effect on metabolic and inflammatory changes induced by a high-fat diet, 10.1096/fj.11-189472
  19. Larter Claire Z, Yeh Matthew M, Van Rooyen Derrick M, Teoh Narci C, Brooling John, Hou Jing Yun, Williams Jacqueline, Clyne Matthew, Nolan Christopher J, Farrell Geoffrey C, Roles of adipose restriction and metabolic factors in progression of steatosis to steatohepatitis in obese, diabetic mice, 10.1111/j.1440-1746.2009.05996.x
  20. Larter Claire Z., Yeh Matthew M., Haigh W. Geoffrey, Van Rooyen Derrick M., Brooling John, Heydet Deborah, Nolan Christopher J., Teoh Narci C., Farrell Geoffrey C., Dietary modification dampens liver inflammation and fibrosis in obesity-related fatty liver disease : Dietary Modification Attenuates Fatty Liver, 10.1002/oby.20123
  21. Van Rooyen Derrick M., Gan Lay T., Yeh Matthew M., Haigh W. Geoffrey, Larter Claire Z., Ioannou George, Teoh Narci C., Farrell Geoffrey C., Pharmacological cholesterol lowering reverses fibrotic NASH in obese, diabetic mice with metabolic syndrome, 10.1016/j.jhep.2013.02.024
  22. Ozcan U., Chemical Chaperones Reduce ER Stress and Restore Glucose Homeostasis in a Mouse Model of Type 2 Diabetes, 10.1126/science.1128294
  23. Lloyd D. J., Wheeler M. C., Gekakis N., A Point Mutation in Sec61 1 Leads to Diabetes and Hepatosteatosis in Mice, 10.2337/db08-1362
  24. Donnelly Kerry L., Smith Coleman I., Schwarzenberg Sarah J., Jessurun Jose, Boldt Mark D., Parks Elizabeth J., Sources of fatty acids stored in liver and secreted via lipoproteins in patients with nonalcoholic fatty liver disease, 10.1172/jci23621
  25. Nakayama Y., Endo M., Tsukano H., Mori M., Oike Y., Gotoh T., Molecular mechanisms of the LPS-induced non-apoptotic ER stress-CHOP pathway, 10.1093/jb/mvp189
  26. Oyadomari S, Mori M, Roles of CHOP/GADD153 in endoplasmic reticulum stress, 10.1038/sj.cdd.4401373
  27. Fornace A J, Nebert D W, Hollander M C, Luethy J D, Papathanasiou M, Fargnoli J, Holbrook N J, Mammalian genes coordinately regulated by growth arrest signals and DNA-damaging agents., 10.1128/mcb.9.10.4196
  28. Schmitt-Ney Michel, Habener Joel F., CHOP/GADD153 Gene Expression Response to Cellular Stresses Inhibited by Prior Exposure to Ultraviolet Light Wavelength Band C (UVC) : INHIBITORY SEQUENCE MEDIATING THE UVC RESPONSE LOCALIZED TO EXON 1, 10.1074/jbc.m007440200
  29. Urano F., Coupling of Stress in the ER to Activation of JNK Protein Kinases by Transmembrane Protein Kinase IRE1, 10.1126/science.287.5453.664
  30. Sharma Manju, Urano Fumihiko, Jaeschke Anja, Cdc42 and Rac1 are major contributors to the saturated fatty acid-stimulated JNK pathway in hepatocytes, 10.1016/j.jhep.2011.03.019
  31. Malhi Harmeet, Bronk Steven F., Werneburg Nathan W., Gores Gregory J., Free Fatty Acids Induce JNK-dependent Hepatocyte Lipoapoptosis, 10.1074/jbc.m510660200
  32. Loria P, Bozzoli M, Concari M, Guicciardi M E, Carubbi F, Bertolotti M, Piani D, Nistri A, Angelico M, Romani M, Carulli N, Effect of taurohyodeoxycholic acid on biliary lipid secretion in humans, 10.1002/hep.510250601
  33. Rinella Mary E., Siddiqui M. Shaddab, Gardikiotes Konstantina, Gottstein Jeanne, Elias Marc, Green Richard M., Dysregulation of the unfolded protein response in db/db mice with diet-induced steatohepatitis, 10.1002/hep.24553
  34. Xu Tian-Ying, Chen Ruo-Hua, Wang Pei, Zhang Ruo-Yu, Ke Sen-Fang, Miao Chao-Yu, 4-Phenyl butyric acid does not generally reduce glucose levels in rodent models of diabetes, 10.1111/j.1440-1681.2009.05328.x
  35. Fu Suneng, Yang Ling, Li Ping, Hofmann Oliver, Dicker Lee, Hide Winston, Lin Xihong, Watkins Steven M., Ivanov Alexander R., Hotamisligil Gökhan S., Aberrant lipid metabolism disrupts calcium homeostasis causing liver endoplasmic reticulum stress in obesity, 10.1038/nature09968
  36. Dentin R., Benhamed F., Hainault I., Fauveau V., Foufelle F., Dyck J. R.B., Girard J., Postic C., Liver-Specific Inhibition of ChREBP Improves Hepatic Steatosis and Insulin Resistance in ob/ob Mice, 10.2337/db06-0200
  37. Shimomura Iichiro, Bashmakov Yuriy, Horton Jay D., Increased Levels of Nuclear SREBP-1c Associated with Fatty Livers in Two Mouse Models of Diabetes Mellitus, 10.1074/jbc.274.42.30028
  38. Henkel A. S., Dewey A. M., Anderson K. A., Olivares S., Green R. M., Reducing endoplasmic reticulum stress does not improve steatohepatitis in mice fed a methionine- and choline-deficient diet, 10.1152/ajpgi.00052.2012
  39. Wu Lian-Ming, Xu Jian-Rong, Hua Jia, Gu Hai-Yan, Zhang Xiao-Fei, Lu Qing, Hu Jia-Ni, Value of diffusion-weighted imaging for the discrimination of pancreatic lesions : a meta-analysis, 10.1097/meg.0b013e32834eff37