MAP1B regulates microtubule dynamics by sequestering EB1/3 in the cytosol of developing neuronal cells

被引:70
作者
Tortosa, Elena [1 ,2 ]
Galjart, Niels [3 ]
Avila, Jesus [1 ,2 ]
Laura Sayas, Carmen [1 ,2 ]
机构
[1] UAM, CSIC, Ctr Biol Mol Severo Ochoa, Dept Mol Neurobiol, Madrid 28049, Spain
[2] Ctr Invest Biomed Red Enfermedades Neurodegenerat, Madrid, Spain
[3] Erasmus MC, Dept Cell Biol & Genet, Rotterdam, Netherlands
关键词
EBs; MAP1B; microtubule dynamics; neuronal development; +TIPs; PLUS-END-TRACKING; PROTEIN; 1B; NERVOUS-SYSTEM; CULTURED NEURONS; BINDING PROTEIN; MESSENGER-RNA; RAT-BRAIN; IN-VITRO; GROWTH; EB3;
D O I
10.1038/emboj.2013.76
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MAP1B, a structural microtubule (MT)-associated protein highly expressed in developing neurons, plays a key role in neurite and axon extension. However, not all molecular mechanisms by which MAP1B controls MT dynamics during these processes have been revealed. Here, we show that MAP1B interacts directly with EB1 and EB3 (EBs), two core 'microtubule plus-end tracking proteins' (+TIPs), and sequesters them in the cytosol of developing neuronal cells. MAP1B overexpression reduces EBs binding to plus-ends, whereas MAP1B downregulation increases binding of EBs to MTs. These alterations in EBs behaviour lead to changes in MT dynamics, in particular overstabilization and looping, in growth cones of MAP1B-deficient neurons. This contributes to growth cone remodelling and a delay in axon outgrowth. Together, our findings define a new and crucial role of MAP1B as a direct regulator of EBs function and MT dynamics during neurite and axon extension. Our data provide a new layer of MT regulation: a classical MAP, which binds to the MT lattice and not to the end, controls effective concentration of core +TIPs thereby regulating MTs at their plus-ends.
引用
收藏
页码:1293 / 1306
页数:14
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