The Lin28/let-7 axis is critical for myelination in the peripheral nervous system

被引:41
作者
Goekbuget, Deniz [1 ]
Pereira, Jorge A. [1 ]
Bachofner, Sven [1 ]
Marchais, Antonin [2 ]
Ciaudo, Constance [1 ]
Stoffel, Markus [1 ]
Schulte, Johannes H. [3 ]
Suter, Ueli [1 ]
机构
[1] ETH, Inst Mol Hlth Sci, Dept Biol, CH-8093 Zurich, Switzerland
[2] ETH, Inst Agr Sci, Dept Biol, CH-8092 Zurich, Switzerland
[3] Childrens Hosp Essen, Dept Pediat Oncol & Haematol, D-45122 Essen, Germany
基金
瑞士国家科学基金会;
关键词
SCHWANN-CELL DIFFERENTIATION; IN-VIVO; MICRORNA; DICER; EXPRESSION; SEQUENCE; ORIGIN; GENES; NOTCH; SOX2;
D O I
10.1038/ncomms9584
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
MicroRNAs (miRNAs) are crucial regulators of myelination in the peripheral nervous system (PNS). However, the miRNAs species involved and the underlying mechanisms are largely unknown. We found that let-7 miRNAs are highly abundant during PNS myelination and that their levels are inversely correlated to the expression of lin28 homolog B (Lin28B), an antagonist of let-7 accumulation. Sustained expression of Lin28B and consequently reduced levels of let-7 miRNAs results in a failure of Schwann cell myelination in transgenic mouse models and in cell culture. Subsequent analyses revealed that let-7 miRNAs promote expression of the myelination-driving master transcription factor Krox20 (also known as Egr2) through suppression of myelination inhibitory Notch signalling. We conclude that the Lin28B/let-7 axis acts as a critical driver of PNS myelination, in particular by regulating myelination onset, identifying this pathway also as a potential therapeutic target in demyelinating diseases.
引用
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页数:9
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