High-resolution imaging demonstrates dynein-based vesicular transport of activated Trk receptors.

A. Bhattacharyya, F. L. Watson, S. Pomeroy, Yan-zhen Zhang, C. Stiles, R. Segal
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引用次数: 102

Abstract

Target-derived neurotrophins signal from nerve endings to the cell body to influence cellular and nuclear responses. The retrograde signal is conveyed by neurotrophin receptors (Trks) themselves. To accomplish this, activated Trks may physically relocalize from nerve endings to the cell bodies. However, alternative signaling mechanisms may also be used. To identify the vehicle wherein the activated Trks are located and transported, and to identify associated motor proteins that would facilitate transport, we use activation-state specific antibodies in concert with immunoelectron microscopy and deconvolution microscopy. We show that the'activated Trks within rat sciatic nerve axons are preferentially localized to coated and uncoated vesicles. These vesicles are moving in a retrograde direction and so accumulate distal to a ligation site. The P-Trk containing vesicles, in turn, colocalize with dynein components, and not with kinesins. Collectively, these results indicate activated Trk within axons travel in vesicles and dynein is the motor that drives these vesicles towards the cell bodies.
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高分辨率成像显示激活的Trk受体基于动力蛋白的囊泡运输。
目标来源的神经营养因子从神经末梢向细胞体发出信号,影响细胞和核反应。逆行信号由神经营养因子受体(Trks)自身传递。为了实现这一目标,激活的Trks可能会从神经末梢重新定位到细胞体。然而,也可以使用替代的信号机制。为了确定激活Trks定位和运输的载体,并确定促进运输的相关运动蛋白,我们使用激活状态特异性抗体,结合免疫电子显微镜和反褶积显微镜。我们发现大鼠坐骨神经轴突内激活的Trks优先定位于包被和未包被的囊泡。这些囊泡逆行运动,因此在结扎部位的远端积聚。反过来,含有P-Trk的囊泡与动力蛋白成分共定位,而不是与动力蛋白共定位。总的来说,这些结果表明轴突内激活的Trk在囊泡中移动,动力蛋白是驱动这些囊泡向细胞体移动的马达。
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