Eine Plattform für die Wissenschaft: Bauingenieurwesen, Architektur und Urbanistik
Eine Plattform für die Wissenschaft: Bauingenieurwesen, Architektur und Urbanistik
A Gallbladder‐Specific Hydrophobic Bile Acid‐FXR‐MUC1 Signaling Axis Mediates Cholesterol Gallstone Formation
https://orcid.org/0000-0002-1343-1323
AbstractDifferences in the distribution of hydrophilic and hydrophobic bile acids (BA) are observed in mouse models of non‐alcoholic fatty liver disease (NAFLD) induced by a high‐fat‐cholesterol “Western‐style” diet (WD), and cholesterol gallstone disease (CGD) induced by a lithogenic diet. Despite sharing common pathological processes, these models exhibit distinct characteristics in their BA pools. The study investigates the impact of hydrophobic BA (HphoBA) and hydrophilic BA (HphilBA) on CGD development using cytochrome‐P450‐2c70 knockout (C70‐KO) mice (miceC70‐KO), genetically modified to resemble humans with a hydrophobic BA pool. All miceC70‐KO fed the WD develop CGD, resembling human cholelithiasis patients, while WD‐fed wild‐type (WT) mice (miceWT) show cholesterol‐saturated bile but rarely form gallstones. Compared to miceWT, WD‐fed miceC70‐KO display caveolae microdomain redistribution in the gallbladder mediated by the HphoBA, FXR, and miR30c/e axis, which enhances the Sp1 transcriptional activity of mucin‐1 (MUC1) genes through nuclear translocation of protein kinase Cζ (PKCζ). These changes contribute to increased production of pronucleating agents (MUC1 and MUC5ac) and accelerate crystallization of gallbladder cholesterol. The data also suggest that WD‐fed miceC70‐KO appropriately model human CGD since lithogenic diet‐fed miceWT have a larger BA pool that masks the negative effects of gallbladder FXR on CGD development.
A Gallbladder‐Specific Hydrophobic Bile Acid‐FXR‐MUC1 Signaling Axis Mediates Cholesterol Gallstone Formation
https://orcid.org/0000-0002-1343-1323
AbstractDifferences in the distribution of hydrophilic and hydrophobic bile acids (BA) are observed in mouse models of non‐alcoholic fatty liver disease (NAFLD) induced by a high‐fat‐cholesterol “Western‐style” diet (WD), and cholesterol gallstone disease (CGD) induced by a lithogenic diet. Despite sharing common pathological processes, these models exhibit distinct characteristics in their BA pools. The study investigates the impact of hydrophobic BA (HphoBA) and hydrophilic BA (HphilBA) on CGD development using cytochrome‐P450‐2c70 knockout (C70‐KO) mice (miceC70‐KO), genetically modified to resemble humans with a hydrophobic BA pool. All miceC70‐KO fed the WD develop CGD, resembling human cholelithiasis patients, while WD‐fed wild‐type (WT) mice (miceWT) show cholesterol‐saturated bile but rarely form gallstones. Compared to miceWT, WD‐fed miceC70‐KO display caveolae microdomain redistribution in the gallbladder mediated by the HphoBA, FXR, and miR30c/e axis, which enhances the Sp1 transcriptional activity of mucin‐1 (MUC1) genes through nuclear translocation of protein kinase Cζ (PKCζ). These changes contribute to increased production of pronucleating agents (MUC1 and MUC5ac) and accelerate crystallization of gallbladder cholesterol. The data also suggest that WD‐fed miceC70‐KO appropriately model human CGD since lithogenic diet‐fed miceWT have a larger BA pool that masks the negative effects of gallbladder FXR on CGD development.
A Gallbladder‐Specific Hydrophobic Bile Acid‐FXR‐MUC1 Signaling Axis Mediates Cholesterol Gallstone Formation
https://orcid.org/0000-0002-1343-1323
AbstractDifferences in the distribution of hydrophilic and hydrophobic bile acids (BA) are observed in mouse models of non‐alcoholic fatty liver disease (NAFLD) induced by a high‐fat‐cholesterol “Western‐style” diet (WD), and cholesterol gallstone disease (CGD) induced by a lithogenic diet. Despite sharing common pathological processes, these models exhibit distinct characteristics in their BA pools. The study investigates the impact of hydrophobic BA (HphoBA) and hydrophilic BA (HphilBA) on CGD development using cytochrome‐P450‐2c70 knockout (C70‐KO) mice (miceC70‐KO), genetically modified to resemble humans with a hydrophobic BA pool. All miceC70‐KO fed the WD develop CGD, resembling human cholelithiasis patients, while WD‐fed wild‐type (WT) mice (miceWT) show cholesterol‐saturated bile but rarely form gallstones. Compared to miceWT, WD‐fed miceC70‐KO display caveolae microdomain redistribution in the gallbladder mediated by the HphoBA, FXR, and miR30c/e axis, which enhances the Sp1 transcriptional activity of mucin‐1 (MUC1) genes through nuclear translocation of protein kinase Cζ (PKCζ). These changes contribute to increased production of pronucleating agents (MUC1 and MUC5ac) and accelerate crystallization of gallbladder cholesterol. The data also suggest that WD‐fed miceC70‐KO appropriately model human CGD since lithogenic diet‐fed miceWT have a larger BA pool that masks the negative effects of gallbladder FXR on CGD development.
A Gallbladder‐Specific Hydrophobic Bile Acid‐FXR‐MUC1 Signaling Axis Mediates Cholesterol Gallstone Formation
Advanced Science
Chen, Hongtan (Autor:in) / Jiang, Xin (Autor:in) / Li, Yiqiao (Autor:in) / Guo, Honggang (Autor:in) / Wu, Jianguo (Autor:in) / Li, Sha (Autor:in) / Hu, Fengling (Autor:in) / Xu, Guoqiang (Autor:in)
11.02.2025
Aufsatz (Zeitschrift)
Elektronische Ressource
Englisch
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