内皮素-1抑制棕色脂肪细胞中脂蛋白脂肪酶基因的表达,而内皮素-3不抑制

Yoko Uchida, Kaoru Irie, Fujiko Tsukahara, Ken-ichi Ohba, Akira Ogawa, Emiko Fujii, Takamura Muraki
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引用次数: 10

摘要

研究了内皮素对培养分化的棕色脂肪细胞脂蛋白脂肪酶活性和脂蛋白脂肪酶mRNA水平的影响。测定两组脂蛋白脂肪酶活性;肝素(10 IU/ml, 1 h)释放到培养基中的脂蛋白脂肪酶(肝素释放部分)和细胞中剩余的脂蛋白脂肪酶活性(可提取表)。时间过程研究表明,内皮素-1(10−7 M)逐渐降低两种脂蛋白脂肪酶组分(肝素释放,可提取),直到24 h时达到最低点。内皮素-1以浓度依赖的方式降低两种脂蛋白脂肪酶活性(肝素释放,可提取),而内皮素-3在这两种酶中都没有产生任何显著变化。Northern blot分析显示,内皮素-1(10−7−10−11 M)在第9天引起细胞中脂蛋白脂肪酶mRNA的浓度依赖性下降。此外,用内皮素ETA受体拮抗剂FR139317预处理棕色脂肪细胞,可以拮抗内皮素1诱导的脂蛋白脂肪酶活性和脂蛋白脂肪酶mRNA的降低。这些结果表明,内皮素-1可能通过细胞膜上的内皮素- ETA受体抑制棕色脂肪细胞的脂蛋白脂肪酶基因表达,从而降低脂蛋白脂肪酶活性。由于作为脂肪分化标志的脂蛋白脂肪酶活性及其mRNA的显著降低,内皮素-1可能在棕色脂肪细胞的分化中具有抑制作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Endothelin-1, but not endothelin-3, suppresses lipoprotein lipase gene expression in brown adipocytes differentiated in culture

The effect of endothelins on lipoprotein lipase activity and lipoprotein lipase mRNA levels was studied in brown adipocytes differentiated in culture. Lipoprotein lipase activity was determined in two fractions; lipoprotein lipase released by heparin (10 IU/ml, 1 h) into the medium (heparin-releasable fraction) and lipoprotein lipase activity remaining in cells (extractable table). Time-course studies showed that endothelin-1 (10−7 M) progressively decreased both lipoprotein lipase fractions (heparin-releasable, extractable), until nadir at 24 h. Endothelin-1 reduced both lipoprotein lipase activities (heparin-releasable, extractable) in a concentration-dependent manner, whereas endothelin-3 did not produce any significant changes in either of them. Northern blot analysis revealed that endothelin-1 (10−7−10−11 M) caused a concentration-dependent decrease in lipoprotein lipase mRNA obtained from cells on day 9. Furthermore, pretreatment of brown adipocytes with endothelin ETA receptor antagonist FR139317 antagonized the endothelin-1-induced reduction of lipoprotein lipase activity and lipoprotein lipase mRNA. These results suggest that endothelin-1 decreases lipoprotein lipase activity by inhibiting the lipoprotein lipase gene expression in brown adipocytes differentiated in culture, possibly through endothelin ETA receptors on cell membranes. Because of marked reduction of lipoprotein lipase activity and its mRNA as a marker of adipogenic differentiation, endothelin-1 may have an inhibitory role in the differentiation of brown adipocytes.

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