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PMID: 11850532 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Tissue distribution and induction of human multidrug resistant protein 3.

Laboratory investigation; a journal of technical methods and pathology ·Vol. 82 ·No. 2 ·2002-02-00 ·Pages 193-201

Scheffer GL, Kool M, de Haas M, de Vree JM, Pijnenborg AC, Bosman DK, Elferink RP, van der Valk P, Borst P, Scheper RJ

Abstract

The multidrug resistance protein (MRP) family consists of several members and, for some of these transporter proteins, distinct roles in multidrug resistance and normal tissue functions have been well established (MRP1 and MRP2) or are still under investigation (MRP3). MRP3 expression studies in human tissues have been largely restricted to the mRNA level. In this report we extended these studies and further explored MRP3 expression at the protein level. Western blot and immunohistochemistry with two MRP3-specific monoclonal antibodies, M(3)II-9 and M(3)II-21, showed MRP3 protein to be present in adrenal gland, and kidney and in tissues of the intestinal tract: colon, pancreas, gallbladder, and liver. In epithelia, MRP3 was found to be located at the basolateral sides of cell membranes. In normal liver, MRP3 was detected at lower levels than anticipated from the mRNA data and was found present mainly in the bile ducts. In livers from patients with various forms of cholestasis, MRP3 levels were frequently increased in the proliferative cholangiocytes, with sometimes additional staining of the basolateral membranes of the hepatocytes. This was especially evident in patients with type 3 progressive familial intrahepatic cholestasis. The present results support the view that MRP3 plays a role in the cholehepatic and enterohepatic circulation of bile and in protection within the biliary tree and tissues along the bile circulation route against toxic bile constituents. The possible functional roles for MRP3 in the adrenal gland and in the kidney remain as yet unknown. In a panel of 34 tumor samples of various histogenetic origins, distinct amounts of MRP3 were detected in a limited number of cases, including lung, ovarian, and pancreatic cancers. These findings may be of potential clinical relevance when considering the drug treatment regimens for these tumor types.

MeSH Terms
Blotting, Western Cholestasis/metabolism Humans Immunohistochemistry Multidrug Resistance-Associated Proteins/biosynthesis,metabolism Neoplasms/metabolism
Chemicals
Multidrug Resistance-Associated Proteins multidrug resistance-associated protein 3
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Scheffer George L
Department of Pathology, Free University Medical Center, Amsterdam, The Netherlands.
Kool Marcel
de Haas Marcel
de Vree J Marleen L
Pijnenborg Adriana C L M
Bosman Diederik K
Elferink Ronald P J Oude
van der Valk Paul
Borst Piet
Scheper Rik J
Article Info
Journal
Laboratory investigation; a journal of technical methods and pathology
Abbr.
Lab Invest
ISSN
0023-6837
Published
2002-02-00
Pages
193-201
Language
English
Region
United States
NLM ID
0376617
Subset
IM
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