Thomou Thomas, Mori Marcelo A, Dreyfuss Jonathan M, Konishi Masahiro, Sakaguchi Masaji, Wolfrum Christian, Rao Tata Nageswara, Winnay Jonathon N, Garcia-Martin Ruben, Grinspoon Steven K, Gorden Phillip, Kahn C Ronald
Section on Integrative Physiology &Metabolism, Joslin Diabetes Center and Harvard Medical School, Boston, Massachusetts, USA.
Department of Biochemistry and Tissue Biology, University of Campinas, Campinas, Brazil.
Nature. 2017 Feb 23;542(7642):450-455. doi: 10.1038/nature21365. Epub 2017 Feb 15.
Adipose tissue is a major site of energy storage and has a role in the regulation of metabolism through the release of adipokines. Here we show that mice with an adipose-tissue-specific knockout of the microRNA (miRNA)-processing enzyme Dicer (ADicerKO), as well as humans with lipodystrophy, exhibit a substantial decrease in levels of circulating exosomal miRNAs. Transplantation of both white and brown adipose tissue-brown especially-into ADicerKO mice restores the level of numerous circulating miRNAs that are associated with an improvement in glucose tolerance and a reduction in hepatic Fgf21 mRNA and circulating FGF21. This gene regulation can be mimicked by the administration of normal, but not ADicerKO, serum exosomes. Expression of a human-specific miRNA in the brown adipose tissue of one mouse in vivo can also regulate its 3' UTR reporter in the liver of another mouse through serum exosomal transfer. Thus, adipose tissue constitutes an important source of circulating exosomal miRNAs, which can regulate gene expression in distant tissues and thereby serve as a previously undescribed form of adipokine.
脂肪组织是能量储存的主要场所,并通过释放脂肪因子在代谢调节中发挥作用。在此我们表明,脂肪组织特异性敲除微小RNA(miRNA)加工酶Dicer的小鼠(ADicerKO)以及患有脂肪营养不良的人类,循环外泌体miRNA水平显著降低。将白色和棕色脂肪组织(尤其是棕色脂肪组织)移植到ADicerKO小鼠体内,可恢复多种循环miRNA的水平,这些miRNA与葡萄糖耐量改善以及肝脏Fgf21 mRNA和循环FGF21减少相关。这种基因调控可通过给予正常血清外泌体而非ADicerKO血清外泌体来模拟。在一只小鼠体内棕色脂肪组织中表达人特异性miRNA,也可通过血清外泌体转移在另一只小鼠肝脏中调节其3' UTR报告基因。因此,脂肪组织构成循环外泌体miRNA的重要来源,其可调节远处组织中的基因表达,从而作为一种此前未被描述的脂肪因子形式。