Phenotypic Determinants of Murine Cholelithiasis

小鼠胆石症的表型决定因素

• 批准号: 6792762
• 负责人: MARTIN CONRAD CAREY
• 金额: $ 22.9万
• 依托单位: BRIGHAM AND WOMEN'S HOSPITAL
• 依托单位国家: 美国
• 财政年份: 1998
• 资助国家: 美国
• 起止时间: 1998-09-01 至 2006-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6792762
• 关键词: RNase protection assay; bilirubin; bilirubin glucuronide; biological transport; cholanate compound; cholecystokinin; cholelithiasis; cholesterol; cystic fibrosis; gastrointestinal absorption /transport; gastrointestinal motility /pressure; genetic polymorphism; genetic susceptibility; laboratory mouse; molecular pathology; neuropeptide receptor; nutrition related tag; pathologic process; phenotype; quantitative trait loci; steroid metabolism; transport proteins; western blottings

DESCRIPTION (provided by applicant): Progress in understanding cholesterol gallstone formation in inbred mice has led to new and continuing specific aims, which are mostly extensions of the previous grant. The principal experimental goals are to identify, characterize and quantify the molecular pathophysiologies and phenotypes involved in murine gallstone formation, particularly those caused by cholesterol gallstone (Lith) genes. Aim I proposes to determine the critical pathophysiological changes that are induced by genetic susceptibility within newly-identified quantitative trait loci (QTL) in genetically-diverse inbred mouse strains. This information will be crucial for identifying positional candidate genes for selected QTL's. Aim 2 will determine whether the proximal biliary tree plays a decisive role in bile lithogenicity and cholesterol gallstone susceptibility induced by the Lith1 locus and establish whether blocking cholehepatic shunting of bile salts prevents cholelithogenesis. Aim 3 will examine efflux transporters and their regulation at the enterocyte level as causes of the augmented cholesterol absorption from the intestine of gallstone-susceptible inbred mice. Aim 4 will investigate the pathogenesis of cholesterol cholelithogenesis in mice with targeted disruption of the cholecystokinin (CCK)-A receptor and carboxypeptidase E, the latter intracellular enzyme processing pro-CCK to CCK; it is anticipated that in addition to biliary dysmotility, there will be small intestinal hypomotility leading to augmented lumenal cholesterol absorption. Aim 5 will elucidate the pathogenesis of pigment gallstones in murine models of cystic fibrosis. The hypothesis predicts a less alkaline bile within the intrahepatic biliary tree and gallbladder with enterohepatic cycling of unconjugated bilirubin from bile salt malabsorption, the latter speculated to be secondary to apical sodium-bile salt co-transporter (ASBT) dysfunction. As a result of a more acidic bile, there will be increased endogenous ?-glucuronidase activity intrahepatically, as well as in the gallbladder, with augmented hydrolysis of bilirubin conjugates resulting in calcium bilirubinate precipitation, thereby leading to "black" pigment gallstones, as well as intrahepatic microprecipitates causing mechanical bile duct obstruction. Because of the close genetic correspondence between mammalian genomes, these pathophysiological studies should lead to more fundamental understanding of these common, as well as economically-significant digestive diseases in human beings.

描述（由申请人提供）：在了解近交系小鼠胆固醇结石形成方面的进展导致了新的和持续的具体目标，这些目标主要是以前资助的扩展。主要的实验目标是确定，表征和量化的分子病理生理学和表型参与鼠胆结石形成，特别是胆固醇结石（Lith）基因引起的。目的确定遗传多样性近交系小鼠中新发现的数量性状位点（QTL）内的遗传易感性诱导的关键病理生理变化。这些信息对于确定所选QTL的位置候选基因是至关重要的。目的2将确定近端胆管树是否在由Lith 1位点诱导的胆汁成石性和胆固醇结石易感性中起决定性作用，并确定阻断胆盐的胆肝分流是否可预防胆石形成。目的3将研究外排转运蛋白及其在肠上皮细胞水平的调节，作为胆固醇从胆结石易感近交系小鼠肠道吸收增加的原因。目的4将研究小鼠胆固醇结石形成的发病机制，靶向破坏胆囊收缩素（CCK）-A受体和羧肽酶E，后者的细胞内酶处理pro-CCK CCK CCK;预计除了胆道动力障碍，小肠动力不足导致管腔胆固醇吸收增加。目的5探讨胆囊色素结石的发病机制。该假设预测肝内胆管树和胆囊内胆汁碱性较低，胆盐吸收不良导致非结合胆红素的肝肠循环，推测后者继发于心尖钠-胆盐共转运蛋白（ASBT）功能障碍。作为一个更酸性胆汁的结果，将有增加内源性？-肝内以及胆囊中的葡萄糖醛酸酶活性增加，胆红素缀合物的水解增加，导致胆红素钙沉淀，从而导致“黑色”色素胆结石，以及肝内微沉淀物引起机械性胆管阻塞。由于哺乳动物基因组之间的密切遗传对应关系，这些病理生理学研究应该导致对这些常见的以及人类经济上重要的消化系统疾病的更基本的理解。