Gene expression of ATP-binding cassette transporters during liver regeneration after 90% hepatectomy in rats
Liver damage with hyperbilirubinemia during regeneration of the small liver is the major hurdle to expand the indications of adult living donor liver transplantation. We performed a large-scale gene expression analysis of the regenerating liver after a 90% hepatectomy in rats, and analyzed the chang...
Gespeichert in:
Veröffentlicht in: | International journal of molecular medicine 2012-07, Vol.30 (1), p.28-34 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Liver damage with hyperbilirubinemia during regeneration of the small liver
is the major hurdle to expand the indications of adult living donor liver transplantation.
We performed a large-scale gene expression analysis of the regenerating liver
after a 90% hepatectomy in rats, and analyzed the changes in the gene expression
patterns related to the ATP-binding cassette (ABC) transporters. RNAs were prepared
from 3 rat livers at 0, 24, 72 and 168 h after a 90% hepatectomy. The gene expression
profile was analyzed by the Rat Genome 230 2.0 array with special references to
the ABC transporters. Among 31,042 probes, 1,587 reported genes were identified
as either upregulated or downregulated more than 2-fold. Among 20 ABC transporter
genes, multidrug resistance protein (MRP) 2 and organic anion transporting polypeptide
(OATP) 1 were significantly downregulated, while MRP1 and MRP3 tended to be expressed.
These genetic changes were confirmed by real-time PCR. A microarray analysis demonstrated
not only an extensive gene expression profile in the regenerating liver but more
specific molecular events related to bilirubin transport at the same time. Changes
in the expression pattern of the ABC transporters, therefore, seem to be the key
event in liver failure during liver regeneration. |
---|---|
ISSN: | 1107-3756 1791-244X |
DOI: | 10.3892/ijmm.2012.972 |