Department of Medical Biochemistry, Faculty of Life Sciences, Kumamoto University, Kumamoto, 860-8556, Japan; Department of Metabolic Medicine, Faculty of Life Sciences, Kumamoto University, Kumamoto, 860-8556, Japan.
Department of Medical Biochemistry, Faculty of Life Sciences, Kumamoto University, Kumamoto, 860-8556, Japan.
Biochem Biophys Res Commun. 2020 Sep 24;530(3):500-507. doi: 10.1016/j.bbrc.2020.05.090. Epub 2020 Jun 25.
Recent evidence has revealed a novel signaling mechanism through which brown adipose tissue (BAT)-derived exosomal microRNAs (miRNAs) influence hepatic gene expression. Here, we uncover neuronal control of these miRNAs and identify exosomal miR-132-3p as a regulator of hepatic lipogenesis under cold stress conditions. Norepinephrine, a sympathetic nervous system neurotransmitter mediating cold-induced BAT activation, altered the composition of brown adipocyte (BAC)-derived exosomal miRNAs; among them, miR-132-3p was significantly induced. The isolated BAC-derived exosomes suppressed expression of hepatic Srebf1, a predicted target of miR-132-3p. In an indirect co-culture system, BACs suppressed expression of hepatic Srebf1 and its target lipogenic genes; this effect was not seen with miR-132-3p-inhibited BACs. Srebf1 was experimentally validated as an miR-132-3p target. Cold stimuli consistently induced miR-132-3p expression in BAT and attenuated Srebf1 expression in the liver. Our results suggest that BAT-derived exosomal miR-132-3p acts as an endocrine factor that regulates hepatic lipogenesis for cold adaptation.
最近的证据揭示了一种新的信号机制,即棕色脂肪组织(BAT)衍生的外泌体 microRNAs(miRNAs)影响肝脏基因表达。在这里,我们揭示了神经元对这些 miRNAs 的控制,并确定外泌体 miR-132-3p 是冷应激条件下肝脏脂肪生成的调节剂。去甲肾上腺素是一种介导冷诱导 BAT 激活的交感神经系统递质,改变了棕色脂肪细胞(BAC)衍生的外泌体 miRNAs 的组成;其中,miR-132-3p 明显被诱导。分离的 BAC 衍生的外泌体抑制了肝脏 Srebf1 的表达,Srebf1 是 miR-132-3p 的一个预测靶点。在间接共培养系统中,BAC 抑制了肝脏 Srebf1 和其靶基因的表达;而 miR-132-3p 抑制的 BAC 则没有这种作用。Srebf1 被实验验证为 miR-132-3p 的靶标。冷刺激一致地诱导 BAT 中 miR-132-3p 的表达,并减弱肝脏中 Srebf1 的表达。我们的结果表明,BAT 衍生的外泌体 miR-132-3p 作为一种内分泌因子,调节肝脏脂肪生成以适应寒冷。