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动力蛋白结合并刺激内体衔接蛋白和NEEP21家族成员钙通道蛋白的轴突运动。

Dynein binds and stimulates axonal motility of the endosome adaptor and NEEP21 family member, calcyon.

作者信息

Shi Liang, Muthusamy Nagendran, Smith Deanna, Bergson Clare

机构信息

Department of Pharmacology and Toxicology, Medical College of Georgia, Augusta University, Augusta, GA, USA.

Department of Neuroscience, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

出版信息

Int J Biochem Cell Biol. 2017 Sep;90:93-102. doi: 10.1016/j.biocel.2017.07.005. Epub 2017 Jul 19.

Abstract

The neuron-enriched, endosomal protein Calcyon (Caly) regulates endocytosis and vesicle sorting, and is important for synaptic plasticity and brain development. In the current investigation of Caly interacting proteins in brain, the microtubule retrograde motor subunit, cytoplasmic dynein 1 heavy chain (DYNC1H), and microtubule structural proteins, α and β tubulin, were identified as Caly associated proteins by MALDI-ToF/ToF. Direct interaction of the Caly-C terminus with dynein and tubulin was further confirmed in in vitro studies. In Cos-7 cells, mCherry-Caly moved along the microtubule network in organelles largely labeled by the late endosome marker Rab7. Expression of the dynein inhibitor CC1, produced striking alterations in Caly distribution, consistent with retrograde motors playing a prominent role in Caly localization and movement. In axons of cultured adult rat sensory neurons, Caly-positive organelles co-localized with dynein intermediate chain (DYNC1I1-isoform IC-1B) and the dynein regulator, lissencephaly 1 (LIS1), both of which co-precipitated from brain with the Caly C-terminus. Manipulation of dynein function in axons altered the motile properties of Caly indicating that Caly vesicles utilize the retrograde motor. Altogether, the current evidence for association with dynein motors raises the possibility that the endocytic and cargo sorting functions of Caly in neurons could be regulated by interaction with the microtubule transport system.

摘要

富含神经元的内体蛋白钙调蛋白(Caly)调节内吞作用和囊泡分选,对突触可塑性和大脑发育至关重要。在当前对大脑中Caly相互作用蛋白的研究中,通过基质辅助激光解吸电离飞行时间质谱/飞行时间质谱(MALDI-ToF/ToF)鉴定出微管逆行运动亚基、胞质动力蛋白1重链(DYNC1H)以及微管结构蛋白α和β微管蛋白为与Caly相关的蛋白。在体外研究中进一步证实了Caly C末端与动力蛋白和微管蛋白的直接相互作用。在Cos-7细胞中,mCherry-Caly沿着主要由晚期内体标记物Rab7标记的细胞器中的微管网络移动。动力蛋白抑制剂CC1的表达使Caly分布产生显著改变,这与逆行运动蛋白在Caly定位和移动中起重要作用一致。在培养的成年大鼠感觉神经元轴突中,Caly阳性细胞器与动力蛋白中间链(DYNC1I1-同工型IC-1B)和动力蛋白调节因子无脑回蛋白1(LIS1)共定位,二者均能从大脑中与Caly C末端共沉淀。对轴突中动力蛋白功能的操纵改变了Caly的运动特性,表明Caly囊泡利用逆行运动蛋白。总之,目前与动力蛋白相关的证据增加了一种可能性,即神经元中Caly的内吞和货物分选功能可能通过与微管运输系统的相互作用来调节。

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