Total parenteral nutrition leads to alteration of hepatocyte cell cycle gene expression and proliferation in the mouse.

Details

Serval ID
serval:BIB_5B9A84B8A888
Type
Article: article from journal or magazin.
Collection
Publications
Title
Total parenteral nutrition leads to alteration of hepatocyte cell cycle gene expression and proliferation in the mouse.
Journal
Digestive Diseases and Sciences
Author(s)
Tazuke Y., Wildhaber B.E., Yang H., Washburn J., Teitelbaum D.H.
ISSN
0163-2116 (Print)
ISSN-L
0163-2116
Publication state
Published
Issued date
2007
Peer-reviewed
Oui
Volume
52
Number
4
Pages
920-930
Language
english
Notes
Publication types: Journal Article ; Research Support, N.I.H., Extramural Publication Status: ppublish
Abstract
Total parenteral nutrition (TPN) is correlated with progressive liver injury. Such injury may be associated with either an increase or decrease in hepatocyte growth. The goal of these experiments was to determine TPN-related alterations in intrahepatic genes, as they relate with the cell cycle, using microarray techniques. After 7 days of infusion of saline or TPN-solution, hepatocyte gene expression was examined with a 5000-cDNA microarray chip. TPN was associated with an up-regulation of the cyclin kinase Cdc25B mRNA, which controls the cell cycle at the G2/M phase. Based on this, our studies were directed at alterations in genes related to mitosis in this phase of the cell cycle. mRNA expression of mitotic phase inducers and inhibitors were examined. Cdc25B1 mRNA expression increased with TPN. TPN also led to additional significant alterations in the expression of other factors which mediate proliferation in this phase of mitosis. Histologically, TPN resulted in a significant decline in hepatocyte proliferation. Coincident with the alteration in cyclin expression was a significant decrease in hepatocytes in the G2/M phase with TPN administration. This study demonstrates significant alterations in cell cycle gene expression with TPN. The findings correlate with a loss of hepatocyte proliferation and may give insight into the potential mechanism of TPN-induced hepatocyte injury.
Keywords
Animals, Apoptosis, Cell Cycle, Cell Cycle Proteins/genetics, Cell Cycle Proteins/metabolism, Cell Proliferation, Cyclins/metabolism, Flow Cytometry, Gene Expression, Genes, cdc, Hepatocytes/cytology, Hepatocytes/metabolism, Male, Mice, Mice, Inbred C57BL, Mitosis, Oligonucleotide Array Sequence Analysis, Parenteral Nutrition, Total/adverse effects, RNA, Messenger/metabolism, cdc25 Phosphatases/genetics
Pubmed
Web of science
Create date
21/02/2015 13:00
Last modification date
20/08/2019 15:14
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