首页> 外文期刊>Biochimica et Biophysica Acta. Molecular and cell biology of Lipids >Lysosomal acid lipase regulates fatty acid channeling in brown adipose tissue to maintain thermogenesis
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Lysosomal acid lipase regulates fatty acid channeling in brown adipose tissue to maintain thermogenesis

机译:溶酶体酸脂肪酶调节棕色脂肪组织中的脂肪酸通道,保持热生成

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摘要

Lysosomal acid lipase (LAL) is the only known enzyme, which hydrolyzes cholesteryl esters and triacylglycerols in lysosomes of multiple cells and tissues. Here, we explored the role of LAL in brown adipose tissue (BAT). LAL-deficient (Lal-/-) mice exhibit markedly reduced UCP1 expression in BAT, modified BAT morphology with accumulation of lysosomes, and mitochondrial dysfunction, consequently leading to regular hypothermic events in mice kept at room temperature. Cold exposure resulted in reduced lipid uptake into BAT, thereby aggravating dyslipidemia and causing life threatening hypothermia in Lal-/- mice. Linking LAL as a potential regulator of lipoprotein lipase activity, we found Angptl4 mRNA expression upregulated in BAT. Our data demonstrate that LAL is critical for shuttling fatty acids derived from circulating lipoproteins to BAT during cold exposure. We conclude that inhibited lysosomal lipid hydrolysis in BAT leads to impaired thermogenesis in Lal-/- mice.
机译:溶酶体酸脂肪酶(LAL)是唯一已知的酶,其在多细胞和组织的溶酶体中水解胆固醇酯和三酰基甘油。 在这里,我们探讨了LAL在棕色脂肪组织(蝙蝠)中的作用。 缺乏缺陷(LAL - / - )小鼠表现出蝙蝠中显着降低的UCP1表达,改性BAT形态与溶酶体积累,并且线粒体功能障碍,因此导致小鼠的常规低温事件保持在室温下。 冷暴露导致脂质摄取降低到蝙蝠中,从而加剧了血脂血症并导致LAL / - 小鼠中的寿命威胁。 将LAL作为脂蛋白脂肪酶活性的潜在调节剂连接,我们发现ANGPTL4 mRNA表达上调在蝙蝠中。 我们的数据表明,LAL对于在冷暴露过程中源于循环脂蛋白衍生给蝙蝠的脂肪酸至关重要。 我们得出结论,抑制蝙蝠中的溶酶体脂质水解导致LAL / - 小鼠的热生成受损。

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