Institute of Molecular Health Sciences, ETH Zurich, Schafmattstrasse 22, HPL H36, 8093 Zurich, Switzerland.
Nat Cell Biol. 2012 Dec;14(12):1330-5. doi: 10.1038/ncb2612.
Brown adipose tissue (BAT) uses the chemical energy of lipids and glucose to produce heat, a function that can be induced by cold exposure or diet. A key regulator of BAT is the gene encoding PR domain containing 16 (Prdm16), whose expression can drive differentiation of myogenic and white fat precursors to brown adipocytes. Here we show that after cold exposure, the muscle-enriched miRNA-133 is markedly downregulated in BAT and subcutaneous white adipose tissue (SAT) as a result of decreased expression of its transcriptional regulator Mef2. miR-133 directly targets and negatively regulates PRDM16, and inhibition of miR-133 or Mef2 promotes differentiation of precursors from BAT and SAT to mature brown adipocytes, thereby leading to increased mitochondrial activity. Forced expression of miR-133 in brown adipogenic conditions prevents the differentiation to brown adipocytes in both BAT and SAT precursors. Our results point to Mef2 and miR-133 as central upstream regulators of Prdm16 and hence of brown adipogenesis in response to cold exposure in BAT and SAT.
棕色脂肪组织(BAT)利用脂质和葡萄糖的化学能量产热,这一功能可通过寒冷暴露或饮食来诱导。BAT 的一个关键调节因子是编码富含 PR 结构域的 16 号基因(Prdm16),其表达可以驱动成肌细胞和白色脂肪前体分化为棕色脂肪细胞。在这里,我们发现,在寒冷暴露后,肌肉丰富的 microRNA-133 在 BAT 和皮下白色脂肪组织(SAT)中的表达明显下调,这是由于其转录调节因子 Mef2 的表达减少所致。miR-133 直接靶向并负调控 PRDM16,抑制 miR-133 或 Mef2 促进来自 BAT 和 SAT 的前体分化为成熟的棕色脂肪细胞,从而导致线粒体活性增加。在棕色脂肪生成条件下强制表达 miR-133 可阻止 BAT 和 SAT 前体向棕色脂肪细胞的分化。我们的研究结果表明,Mef2 和 miR-133 是 Prdm16 的核心上游调节因子,因此是 BAT 和 SAT 中对寒冷暴露的棕色脂肪生成的反应的关键调节因子。