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An evaluation of the mechanism of ABCA7 on cellular lipid release in ABCA7-HEC293 cell

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收录情况: ◇ SCIE ◇ 统计源期刊 ◇ CSCD-C ◇ 中华系列

机构: [1]Beijing Inst Traumatol & Orthopaed, Dept Mol Orthopaed, Beijing 100035, Peoples R China; [2]Beijing Inst Heart Lung & Blood Vessel Dis, Beijing 100035, Peoples R China
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关键词: ATP-binding cassette transporter A7 ATP-binding cassette transporter A1 lipid release

摘要:
Background ABCA7 is a member of the ABCA subfamily that shows a high degree of homology to ABCA1 and, like ABCA1, mediates cellular cholesterol and phospholipid release by apolipoproteins when transfected in vitro. However, expression of ABCA7 has been shown to be downregulated by increased cellular cholesterol while ABCA1 was upregulated. Methods The underlying mechanism for this effect was examined in ABCA1 or ABCA7-transfected HEC293. Lipid content in the medium and cells was determined by enzymatic assays. Gene expression was quantitated by real time PCR, and protein content was determined by Western blotting. Results While ABCA7 mRNA was decreased by 25-hydroxycholesterol treatment, ABCA1 was apparently increased. Treatment with the synthetic LXR agonist T0901317 (T09) upregulated ABCA1 expression and apoAl-mediated cellular lipid release in ABCA1-transfected HEC293 cells, but ABCA7 expression and cellular lipid release in ABCA7-transfected HEC293 cells showed no obvious changes. Conclusion The ABCA7 gene is regulated by sterol in a direction opposite to that of ABCA1.

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出版当年[2012]版:
大类 | 4 区 医学
小类 | 4 区 医学:内科
最新[2023]版:
大类 | 3 区 医学
小类 | 3 区 医学:内科
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出版当年[2011]版:
Q3 MEDICINE, GENERAL & INTERNAL
最新[2023]版:
Q1 MEDICINE, GENERAL & INTERNAL

影响因子: 最新[2023版] 最新五年平均 出版当年[2011版] 出版当年五年平均 出版前一年[2010版] 出版后一年[2012版]

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第一作者机构: [1]Beijing Inst Traumatol & Orthopaed, Dept Mol Orthopaed, Beijing 100035, Peoples R China; [2]Beijing Inst Heart Lung & Blood Vessel Dis, Beijing 100035, Peoples R China
通讯作者:
通讯机构: [1]Beijing Inst Traumatol & Orthopaed, Dept Mol Orthopaed, Beijing 100035, Peoples R China; [2]Beijing Inst Heart Lung & Blood Vessel Dis, Beijing 100035, Peoples R China
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