目的探討肝細胞膽管膜上轉運子BSEP、MRP2和MDR3與膽囊膽固醇結石形成的關系。
方法收集膽囊膽固醇結石患者的肝組織標本20例,正常肝組織標本10例。應用逆轉錄聚合酶鏈反應(RTPCR)技術和Western blot技術檢測BSEP、MRP2及MDR3 mRNA和蛋白的表達。
結果膽囊膽固醇結石患者肝組織中BSEP、MRP2和MDR3 的mRNA及蛋白表達均顯著低于正常肝組織(P<0.01)。
結論 BSEP、MRP2和MDR3的表達降低可能與膽囊膽固醇結石的形成有關。
引用本文: 孔凡民,隋春陽,李航宇,李昱驥,孫宏治,郭仁宣,郭克建,田雨霖. 膽囊膽固醇結石與肝細胞膽管膜上轉運子BSEP、MRP2和MDR3關系的研究. 中國普外基礎與臨床雜志, 2006, 13(3): 314-316. doi: 復制
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- 2. van BergeHenegouwen GP, Venneman NG, Portincasa P, et al. Relevance of hereditary defects in lipid transport proteins for the pathogenesis of cholesterol gallstone disease.
- 3. Trauner M, Boyer JL. Bile salt transporters: molecular characterization, function, and regulation [J]. Physiol Rev, 2003; 83(2)∶633.
- 4. Hoda F, Green RM. Hepatic canalicular membrane transport of bile salt in C57L/J and AKR/J mice: implications for cholesterol gallstone formation [J]. J Membr Biol, 2003; 196(1)∶9.
- 5. Huang L, Zhao A, Lew JL, et al. Farnesoid X receptor activates transcription of the phospholipid pump MDR3 [J]. J Biol Chem, 2003; 278(51)∶51085.
- 6. Meier PJ, Stieger B. Bile salt transporters [J]. Annu Rev Physiol, 2002; 64(2)∶635.
- 7. Plass JR, Mol O, Heegsma J, et al. A progressive familial intrahepatic cholestasis type 2 mutation causes an unstable, temperaturesensitive bile salt export pump [J]. J Hepatol, 2004; 40(1)∶24.
- 8. Fickert P, Fuchsbichler A, Wagner M, et al. Regurgitation of bile acids from leaky bile ducts causes sclerosing cholangitis in Mdr2 (Abcb4) knockout mice [J]. Gastroenterology, 2004; 127(1)∶261.
- 9. Shoda J, Oda K, Suzuki H, et al. Etiologic significance of defects in cholesterol, phospholipid, and bile acid metabolism in the liver of patients with intrahepatic calculi [J]. Hepatology, 2001; 33(5)∶1194.
- 10. Smit JJ, Schinkel AH, Oude Elferink RP, et al. Homozygous disruption of the murine mdr2 Pglycoprotein gene leads to a complete absence of phospholipid from bile and to liver disease [J]. Cell, 1993; 75(3)∶451.
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