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Tissue distribution and induction of human multidrug resistant protein 3
George L Scheffer1, Marcel Kool, Marcel de Haas
1Department of Pathology, Free University Medical Center, Amsterdam, The Netherlands.
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.
Insights
Multidrug resistance protein 3 (MRP3) is found in human tissues like the liver and intestines. MRP3 protein levels increase in cholestasis, suggesting a role in bile circulation and protection against toxic bile constituents.
Area of Science:
- Biochemistry
- Molecular Biology
- Cell Biology
Background:
- The multidrug resistance protein (MRP) family includes transporter proteins with established roles in drug resistance and normal tissue functions.
- While MRP1 and MRP2 functions are well-defined, the roles of other members like MRP3 are still under investigation.
- Previous MRP3 expression studies were primarily limited to the mRNA level in human tissues.
Purpose of the Study:
- To investigate the protein-level expression of MRP3 in various human tissues.
- To determine the cellular localization of MRP3 protein.
- To explore the potential role of MRP3 in cholestasis and cancer.
Main Methods:
- Western blot analysis using MRP3-specific monoclonal antibodies (M(3)II-9 and M(3)II-21).
- Immunohistochemistry to visualize MRP3 protein distribution in tissue samples.
- Analysis of tumor samples from various histogenetic origins.
Main Results:
- MRP3 protein was detected in the adrenal gland, kidney, and intestinal tract tissues (colon, pancreas, gallbladder, liver).
- MRP3 localizes to the basolateral sides of cell membranes in epithelia.
- In normal liver, MRP3 was found mainly in bile ducts at lower levels than expected from mRNA data.
- MRP3 levels were elevated in cholangiocytes and sometimes hepatocytes in cholestatic livers, particularly in progressive familial intrahepatic cholestasis.
- MRP3 was detected in a limited number of lung, ovarian, and pancreatic cancers.
Conclusions:
- MRP3 protein expression is present in various human tissues, with specific localization patterns.
- Increased MRP3 in cholestasis suggests a role in bile circulation and protection against toxic bile constituents.
- MRP3 expression in certain cancers may have clinical relevance for drug treatment strategies.