| Project/Area Number |
23659142
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| Research Category |
Grant-in-Aid for Challenging Exploratory Research
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| Allocation Type | Multi-year Fund |
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| Research Field |
General pharmacology
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| Research Institution | Toho University |
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Principal Investigator |
AKAHANE Satomi (ADACHI Satomi) 東邦大学, 医学部, 准教授 (00184185)
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| Co-Investigator(Kenkyū-buntansha) |
NAKASEKO Hiroko (IZUMI Hiroko) 東邦大学, 医学部, 助教 (80408773)
ITO Masanori 東邦大学, 医学部, 助教 (20459811)
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| Project Period (FY) |
2011 – 2012
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| Project Status |
Completed (Fiscal Year 2012)
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| Budget Amount *help |
¥3,770,000 (Direct Cost: ¥2,900,000、Indirect Cost: ¥870,000)
Fiscal Year 2012: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2011: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
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| Keywords | 脂質代謝 / 胆汁酸 / コレステロール / トリグリセリド / 肝臓 / 脂質転移蛋白 / マウス / リポ蛋白 |
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| Research Abstract |
STARD10, a member of the steroidogenic acute regulatory protein (StAR)-related lipid transfer (START) protein family, is highly expressed in the liver and has been shown to transfer phosphatidylcholine. Therefore it has been assumed that STARD10 may function in the secretion of phospholipids into the bile. To help elucidate the physiological role of STARD10, we produced Stard10knockout mice (Stard10^-/-) and studied their phenotype.Neither liver content nor biliary secretion of phosphatidylcholine was altered in Stard10^-/-mice. Unexpectedly, the biliary secretion of bile acids from the liver and the level of taurine-conjugated bile acids in bile were significantly higher in Stard10^-/-mice than wild type (WT) mice.In contrast, the levels of the secondary bile acids were lower in the liver of Stard10-/-mice, suggesting that the enterohepatic cycling is impaired.STARD10 was also expressed in the gallbladder and small intestine where the expression level of apical sodium dependent bile acid transporter (ASBT) turned out to be markedly lower in Stard10^-/-mice than in WT mice when measured under fed condition.Consistent with the above results, the fecal excretion of bile acids was significantly increased in Stard10^-/-mice. Interestingly, PPARa-dependent genes responsible for the regulation of bile acid metabolism were down-regulated in the liver of Stard10^-/-mice.The loss of STARD10 impaired the PPARa activity and the expression of a PPARa-target gene such as Cyp8b1in mouse hepatoma cells. These results indicate that STARD10 is involved in regulating bile acid metabolism through the modulation of PPARa-mediated mechanism.
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