Literature DB >> 20551477

Time course gene expression using laser capture microscopy-extracted bile ducts, but not hepatic parenchyma, reveals acute alpha-naphthylisothiocyanate toxicity.

John Michael Cullen1, James Greg Falls, Harlan Roger Brown, Lawrence Wonsik Yoon, Neal Foster Cariello, Brenda Faiola, Carie Lynette Kimbrough, Holly Lynn Jordan, Richard Thomas Miller.   

Abstract

Acute toxic responses to a 50-mg/kg oral dose of 1-naphthylisothiocyanate (ANIT) were evaluated by microarray analysis of laser capture-microdissected rat biliary epithelium or hepatic parenchyma obtained 2 and 6 hours postdose. Distinct differences in gene expression patterns between biliary epithelium and hepatic parenchyma were noted at the 2-hour postdose time point, where 375 genes were altered in biliary epithelium but only 38 genes were altered in hepatic parenchyma. Endoplasmic reticulum stress genes were uniquely expressed in biliary epithelial cells at 2 hours postdose. By 6 hours postdose, 620 genes were altered in biliary epithelium, but only 32 genes were altered in hepatic parenchyma. In biliary epithelium, expression of genes involved in the unfolded protein response had decreased compared with the 2-hour time point, while expression of genes involved in protein degradation such as proteasome-ubquination pathways and cell death pathways had increased. At this same time, hepatic parenchymal gene expression changed little. Within 6 hours following oral exposure to ANIT, prior to morphologic changes, specific biliary epithelial gene expression changes, indicative of a vigorous unfolded protein response with protein destruction and cell death pathway activation were noted, in contrast to minor changes in the hepatic parenchyma.

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Year:  2010        PMID: 20551477     DOI: 10.1177/0192623310373774

Source DB:  PubMed          Journal:  Toxicol Pathol        ISSN: 0192-6233            Impact factor:   1.902


  5 in total

1.  Characterization of acute biliary hyperplasia in Fisher 344 rats administered the indole-3-carbinol analog, NSC-743380.

Authors:  Sandy R Eldridge; Joseph Covey; Joel Morris; Bingliang Fang; Thomas L Horn; Karen E Elsass; John R Hamre; David L McCormick; Myrtle A Davis
Journal:  Toxicol Appl Pharmacol       Date:  2014-10-28       Impact factor: 4.219

2.  Gender-specific reduction of hepatic Mrp2 expression by high-fat diet protects female mice from ANIT toxicity.

Authors:  Bo Kong; Iván L Csanaky; Lauren M Aleksunes; Meghan Patni; Qi Chen; Xiaochao Ma; Hartmut Jaeschke; Scott Weir; Melinda Broward; Curtis D Klaassen; Grace L Guo
Journal:  Toxicol Appl Pharmacol       Date:  2012-04-11       Impact factor: 4.219

3.  Comedications alter drug-induced liver injury reporting frequency: Data mining in the WHO VigiBase™.

Authors:  Ayako Suzuki; Nancy A Yuen; Katarina Ilic; Richard T Miller; Melinda J Reese; H Roger Brown; Jeffrey I Ambroso; J Gregory Falls; Christine M Hunt
Journal:  Regul Toxicol Pharmacol       Date:  2015-05-16       Impact factor: 3.271

4.  Beyond miR-122: Identification of MicroRNA Alterations in Blood During a Time Course of Hepatobiliary Injury and Biliary Hyperplasia in Rats.

Authors:  Rachel J Church; Monicah Otieno; James Eric McDuffie; Bhanu Singh; Manisha Sonee; LeRoy Hall; Paul B Watkins; Heidrun Ellinger-Ziegelbauer; Alison H Harrill
Journal:  Toxicol Sci       Date:  2015-11-26       Impact factor: 4.849

5.  Dynamics of hepatocyte-cholangiocyte cell-fate decisions during liver development and regeneration.

Authors:  Sarthak Sahoo; Ashutosh Mishra; Anna Mae Diehl; Mohit Kumar Jolly
Journal:  iScience       Date:  2022-08-18
  5 in total

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