Expression of MRP2 and MDR1 Transporters and Other Hepatic Markers in Rat and Human Liver and in WRL 68 Cell Line

Title:

Expression of MRP2 and MDR1 Transporters and Other Hepatic Markers in Rat and Human Liver and in WRL 68 Cell Line

Creator:

Čížková, D., Mokrý, J., Mičuda, S., Österreicher, J., and Martínková, J.

Identifier:

https://cdk.lib.cas.cz/client/handle/uuid:bd375036-50ef-45ed-bd94-edd5a571a4ad
uuid:bd375036-50ef-45ed-bd94-edd5a571a4ad

Subject:

MRP2 protein, MDR 1 protein, WRL 68 cell line, Liver, and Immunohistochemistry

Type:

article, model:article, and TEXT

Description:

Here we describe a comparative study of phenotypic properties of hepatic cells in situ and in vitro. We analyzed the expression levels and distribution patterns of ABC transporters MRP2 and MDR1, pan-cytokeratin, cytokeratin 18, albumin, alpha-fetoprotein and the specific hepatocyte marker OCH1E5 in the fetal and adult rat as well as human liver tissue and in human fetal hepatocytes of WRL 68 cell line using peroxidase immunohistochemistry or immunofluorescence. Transporters MRP2 and MDR1 were expressed in all examined liver tissues, except rat ED13 embryo. The immunopositivity of these proteins was localized to the canalicular membrane of differentiating and mature hepatocytes but in the later developmental stages and in the adult liver tissues it was also found in the apical membrane of cholangiocytes. In WRL 68 cells, MRP2 and MDR1 immunoreactivity appeared after 5-6 days of cultivation and both transporters were fully expressed in the plasmalemma and in the cytoplasm 9 days after the passage. In conclusion, we observed only moderate variances reflecting diverse ontogenetic phases between the fetal and adult liver tissue. To study functions of hepatocytes in vitro, WRL 68 cells have to differentiate prior to the examination. Our findings indicate that WRL 68 cells can undergo differentiation in vitro and their antigenic profile closely resembles hepatocytes in the human liver.

Language:

English

Rights:

http://creativecommons.org/licenses/by-nc-sa/4.0/
policy:public

Source:

Physiological research | 2005 Volume:54 | Number:4

Harvested from:

CDK

Metadata only:

false