Department of Human Genetics, University of Utah School of Medicine, Salt Lake City, Utah, USA.
Dev Dyn. 2021 May;250(5):640-651. doi: 10.1002/dvdy.287. Epub 2021 Jan 9.
Lipid levels are maintained by balancing lipid uptake, synthesis, and mobilization. Although many studies have focused on the control of lipid synthesis and mobilization, less is known about the regulation of lipid digestion and uptake.
Here we show that the Drosophila E78A nuclear receptor plays a central role in intestinal lipid homeostasis through regulation of the CG17192 digestive lipase. E78A mutant adults fail to maintain proper systemic lipid levels following eclosion, with this effect largely restricted to the intestine. Transcriptional profiling by RNA-seq revealed a candidate gene for mediating this effect, encoding the predicted adult intestinal lipase CG17192. Intestine-specific disruption of CG17192 results in reduced lipid levels similar to that seen in E78A mutants. In addition, dietary supplementation with free fatty acids, or intestine-specific expression of either E78A or CG17192, is sufficient to restore lipid levels in E78A mutant adults.
These studies support the model that E78A is a central regulator of adult lipid homeostasis through its effects on CG17192 expression and lipid digestion. This work also provides new insights into the control of intestinal lipid uptake and demonstrate that nuclear receptors can play an important role in these pathways.
脂质水平通过脂质摄取、合成和动员的平衡来维持。尽管许多研究都集中在脂质合成和动员的控制上,但对于脂质消化和摄取的调节知之甚少。
在这里,我们展示了果蝇 E78A 核受体通过调节 CG17192 消化脂肪酶在肠道脂质稳态中发挥核心作用。E78A 突变体成虫在羽化后无法维持适当的全身脂质水平,这种影响主要局限于肠道。通过 RNA-seq 进行的转录谱分析揭示了一个介导这种效应的候选基因,该基因编码预测的成年肠道脂肪酶 CG17192。CG17192 的肠道特异性缺失导致脂质水平降低,类似于 E78A 突变体中观察到的情况。此外,用游离脂肪酸进行饮食补充,或在肠道特异性表达 E78A 或 CG17192,足以恢复 E78A 突变体成虫中的脂质水平。
这些研究支持 E78A 通过其对 CG17192 表达和脂质消化的影响,成为调节成年脂质稳态的核心调节剂的模型。这项工作还为肠道脂质摄取的控制提供了新的见解,并表明核受体可以在这些途径中发挥重要作用。