Altered remodeling of nucleolar machineries in cultured hepatocytes treated with thioacetamide.

Thioacetamide (TA) is converted into a hyperacetylating agent which causes hepatic necrosis, regeneration, cirrhosis and cancerous transformation. One of the most characteristic toxicities of TA in rat is observed with a 50 mg/kg per day which induces nucleolar enlargement different from that in reg...

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Main Authors: Jeong, J. S., Han, S. Y., Kim, Y. H., Choi, Y. C.
Format: Online
Language:English
Published: Korean Academy of Medical Sciences 2001
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054557/
id pubmed-3054557
recordtype oai_dc
spelling pubmed-30545572011-03-15 Altered remodeling of nucleolar machineries in cultured hepatocytes treated with thioacetamide. Jeong, J. S. Han, S. Y. Kim, Y. H. Choi, Y. C. Research Article Thioacetamide (TA) is converted into a hyperacetylating agent which causes hepatic necrosis, regeneration, cirrhosis and cancerous transformation. One of the most characteristic toxicities of TA in rat is observed with a 50 mg/kg per day which induces nucleolar enlargement different from that in regenerating liver. From TA-treated liver, the nucleoli were isolated and characterized for an altered nucleolar signal transduction system. Immunochemistry revealed that the poisoned nucleoli had increased levels of both nucleolus specific proteins (nucleophosmin and nucleolin) and various signal molecules (CK2, Erk1/2, p38, protein kinases A and C, and cyclin A). Using flow cytometry, the nucleoli were found to be in G2-arrested nuclei. Manifestation of the nucleolar enlargement could be readily observed using an ex vivo hepatocyte culture. There were two types of nucleolar enlargement. One was observed in normal hepatocytes with light density of enlarged nucleoli. The other was in TA-treated hepatocytes with dense and compact density of enlarged nucleoli, which contained a 3 to 5-fold higher nudeophosmin content than the control. In vitro induction of nucleolar enlargement with TA was possible. As soon as the hepatocytes anchored on a collagen coat, exogeneous TA (higher than 1 microg/mL) could induce dense and compact nucleoli. However, when an exogeneous drug was added after monolayer formation (1 day), no drug-induced nucleolar enlargement was observed. Korean Academy of Medical Sciences 2001-02 /pmc/articles/PMC3054557/ /pubmed/11289405 Text en
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Jeong, J. S.
Han, S. Y.
Kim, Y. H.
Choi, Y. C.
spellingShingle Jeong, J. S.
Han, S. Y.
Kim, Y. H.
Choi, Y. C.
Altered remodeling of nucleolar machineries in cultured hepatocytes treated with thioacetamide.
author_facet Jeong, J. S.
Han, S. Y.
Kim, Y. H.
Choi, Y. C.
author_sort Jeong, J. S.
title Altered remodeling of nucleolar machineries in cultured hepatocytes treated with thioacetamide.
title_short Altered remodeling of nucleolar machineries in cultured hepatocytes treated with thioacetamide.
title_full Altered remodeling of nucleolar machineries in cultured hepatocytes treated with thioacetamide.
title_fullStr Altered remodeling of nucleolar machineries in cultured hepatocytes treated with thioacetamide.
title_full_unstemmed Altered remodeling of nucleolar machineries in cultured hepatocytes treated with thioacetamide.
title_sort altered remodeling of nucleolar machineries in cultured hepatocytes treated with thioacetamide.
description Thioacetamide (TA) is converted into a hyperacetylating agent which causes hepatic necrosis, regeneration, cirrhosis and cancerous transformation. One of the most characteristic toxicities of TA in rat is observed with a 50 mg/kg per day which induces nucleolar enlargement different from that in regenerating liver. From TA-treated liver, the nucleoli were isolated and characterized for an altered nucleolar signal transduction system. Immunochemistry revealed that the poisoned nucleoli had increased levels of both nucleolus specific proteins (nucleophosmin and nucleolin) and various signal molecules (CK2, Erk1/2, p38, protein kinases A and C, and cyclin A). Using flow cytometry, the nucleoli were found to be in G2-arrested nuclei. Manifestation of the nucleolar enlargement could be readily observed using an ex vivo hepatocyte culture. There were two types of nucleolar enlargement. One was observed in normal hepatocytes with light density of enlarged nucleoli. The other was in TA-treated hepatocytes with dense and compact density of enlarged nucleoli, which contained a 3 to 5-fold higher nudeophosmin content than the control. In vitro induction of nucleolar enlargement with TA was possible. As soon as the hepatocytes anchored on a collagen coat, exogeneous TA (higher than 1 microg/mL) could induce dense and compact nucleoli. However, when an exogeneous drug was added after monolayer formation (1 day), no drug-induced nucleolar enlargement was observed.
publisher Korean Academy of Medical Sciences
publishDate 2001
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054557/
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