Dicer1 and miR-219 Are Required for Normal Oligodendrocyte Differentiation and Myelination

被引:484
作者
Dugas, Jason C. [1 ]
Cuellar, Trinna L. [2 ]
Scholze, Anja [1 ]
Ason, Brandon [2 ]
Ibrahim, Adiljan [1 ]
Emery, Ben [1 ]
Zamanian, Jennifer L. [1 ]
Foo, Lynette C. [1 ]
McManus, Michael T. [2 ]
Barres, Ben A. [1 ]
机构
[1] Stanford Univ, Dept Neurobiol, Sch Med, Stanford, CA 94305 USA
[2] Univ Calif San Francisco, Ctr Diabet, San Francisco, CA 94143 USA
关键词
GLIAL PROGENITOR-CELL; MICRORNA EXPRESSION; GROWTH-FACTOR; TRANSCRIPTION FACTORS; NERVOUS-SYSTEM; CYCLE EXIT; PROTEIN; IDENTIFICATION; LINEAGE; NEURONS;
D O I
10.1016/j.neuron.2010.01.027
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
To investigate the role of microRNAs in regulating oligodendrocyte (OL) differentiation and myelination, we utilized transgenic mice in which microRNA processing was disrupted in OL precursor cells (OPCs) and OLs by targeted deletion of Dicer1. We found that inhibition of OPC-OL miRNA processing disrupts normal CNS myelination and that OPCs lacking mature miRNAs fail to differentiate normally in vitro. We identified three miRNAs (miR-219, miR-138, and miR-338) that are induced 10-100x during OL differentiation; the most strongly induced of these, miR-219, is necessary and sufficient to promote OL differentiation, and partially rescues OL differentiation defects caused by total miRNA loss. miR-219 directly represses the expression of PDGFR alpha, Sox6, FoxJ3, and ZFP238 proteins, all of which normally help to promote OPC proliferation. Together, these findings show that miR-219 plays a critical role in coupling differentiation to proliferation arrest in the OL lineage, enabling the rapid transition from proliferating OPCs to myelinating OLs.
引用
收藏
页码:597 / 611
页数:15
相关论文
共 58 条
[1]   RP58 associates with condensed chromatin and mediates a sequence-specific transcriptional repression [J].
Aoki, K ;
Meng, GY ;
Suzuki, K ;
Takashi, T ;
Kameoka, Y ;
Nakahara, K ;
Ishida, R ;
Kasai, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (41) :26698-26704
[2]   PDGF Stimulates the Massive Expansion of Glial Progenitors in the Neonatal Forebrain [J].
Assanah, M. C. ;
Bruce, J. N. ;
Suzuki, S. O. ;
Chen, A. ;
Goldman, J. E. ;
Canoll, P. .
GLIA, 2009, 57 (16) :1835-1847
[3]   Glial progenitors in adult white matter are driven to form malignant gliomas by platelet-derived growth factor-expressing retroviruses [J].
Assanah, Marcela ;
Lochhead, Richard ;
Ogden, Alfred ;
Bruce, Jeffrey ;
Goldman, James ;
Canoll, Peter .
JOURNAL OF NEUROSCIENCE, 2006, 26 (25) :6781-6790
[4]   CONTROL OF OLIGODENDROCYTE NUMBER IN THE DEVELOPING RAT OPTIC-NERVE [J].
BARRES, BA ;
RAFF, MC .
NEURON, 1994, 12 (05) :935-942
[5]  
BARRES BA, 1993, DEVELOPMENT, V118, P283
[6]  
BARRES BA, 1994, DEVELOPMENT, V120, P1097
[7]   MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[8]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[9]   Biology of oligodendrocyte and myelin in the mammalian central nervous system [J].
Baumann, N ;
Pham-Dinh, D .
PHYSIOLOGICAL REVIEWS, 2001, 81 (02) :871-927
[10]   PLATELET-DERIVED GROWTH-FACTOR IS A MITOGEN FOR GLIAL BUT NOT FOR NEURONAL RAT-BRAIN CELLS-INVITRO [J].
BESNARD, F ;
PERRAUD, F ;
SENSENBRENNER, M ;
LABOURDETTE, G .
NEUROSCIENCE LETTERS, 1987, 73 (03) :287-292