Department of General Internal Medicine, Endocrinology and Metabolic Diseases, Leiden University Medical Center, Leiden, The Netherlands.
J Lipid Res. 2013 Feb;54(2):448-56. doi: 10.1194/jlr.M031963. Epub 2012 Nov 17.
Caspase-1 is known to activate the proinflammatory cytokines IL-1β and IL-18. Additionally, it can cleave other substrates, including proteins involved in metabolism. Recently, we showed that caspase-1 deficiency in mice strongly reduces high-fat diet-induced weight gain, at least partly caused by an increased energy production. Increased feces secretion by caspase-1-deficient mice suggests that lipid malabsorption possibly further reduces adipose tissue mass. In this study we investigated whether caspase-1 plays a role in triglyceride-(TG)-rich lipoprotein metabolism using caspase-1-deficient and wild-type mice. Caspase-1 deficiency reduced the postprandial TG response to an oral lipid load, whereas TG-derived fatty acid (FA) uptake by peripheral tissues was not affected, demonstrated by unaltered kinetics of [(3)H]TG-labeled very low-density lipoprotein (VLDL)-like emulsion particles. An oral gavage of [(3)H]TG-containing olive oil revealed that caspase-1 deficiency reduced TG absorption and subsequent uptake of TG-derived FA in liver, muscle, and adipose tissue. Similarly, despite an elevated hepatic TG content, caspase-1 deficiency reduced hepatic VLDL-TG production. Intestinal and hepatic gene expression analysis revealed that caspase-1 deficiency did not affect FA oxidation or FA uptake but rather reduced intracellular FA transport, thereby limiting lipid availability for the assembly and secretion of TG-rich lipoproteins. The current study reveals a novel function for caspase-1, or caspase-1-cleaved substrates, in controlling intestinal TG absorption and hepatic TG secretion.
半胱天冬酶-1 已知能激活前炎性细胞因子白细胞介素-1β和白细胞介素-18。此外,它还可以切割其他底物,包括参与代谢的蛋白质。最近,我们发现,小鼠中半胱天冬酶-1 的缺乏强烈地减少了高脂肪饮食诱导的体重增加,至少部分原因是能量产生增加。缺乏半胱天冬酶-1 的小鼠的粪便分泌增加表明脂质吸收不良可能进一步减少脂肪组织质量。在这项研究中,我们使用缺乏半胱天冬酶-1 的和野生型的小鼠来研究半胱天冬酶-1 是否在富含甘油三酯(TG)的脂蛋白代谢中发挥作用。半胱天冬酶-1 的缺乏减少了口服脂质负荷后的 TG 反应,而外周组织对 TG 衍生的脂肪酸(FA)的摄取不受影响,这可以通过未改变的[(3)H]TG 标记的极低密度脂蛋白(VLDL)样乳剂颗粒动力学来证明。口服[(3)H]TG 含有橄榄油表明,半胱天冬酶-1 的缺乏减少了 TG 的吸收和随后在肝脏、肌肉和脂肪组织中 TG 衍生的 FA 的摄取。同样,尽管肝 TG 含量升高,但半胱天冬酶-1 的缺乏减少了肝 VLDL-TG 的产生。肠道和肝脏的基因表达分析表明,半胱天冬酶-1 的缺乏不影响 FA 氧化或 FA 摄取,而是减少细胞内 FA 转运,从而限制了组装和分泌富含 TG 的脂蛋白的脂质可用性。本研究揭示了半胱天冬酶-1 或半胱天冬酶-1 切割的底物在控制肠道 TG 吸收和肝脏 TG 分泌中的新功能。