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本文引用的文献

1
Polarization-modulated differential-interference contrast microscopy with a variable retarder.带有可变延迟器的偏振调制微分干涉对比显微镜。
Appl Opt. 2000 Dec 1;39(34):6288-94. doi: 10.1364/ao.39.006288.
2
Axonal transport and neurodegenerative disease.轴突运输与神经退行性疾病
Biochim Biophys Acta. 2006 Nov-Dec;1762(11-12):1094-108. doi: 10.1016/j.bbadis.2006.04.002. Epub 2006 Apr 19.
3
Organelle transport along microtubules in Xenopus melanophores: evidence for cooperation between multiple motors.非洲爪蟾黑素细胞中细胞器沿微管的运输:多个马达蛋白协同作用的证据
Biophys J. 2006 Jan 1;90(1):318-27. doi: 10.1529/biophysj.105.067843. Epub 2005 Oct 7.
4
Kinesin and dynein move a peroxisome in vivo: a tug-of-war or coordinated movement?驱动蛋白和动力蛋白在体内移动过氧化物酶体:拔河比赛还是协同运动?
Science. 2005 Jun 3;308(5727):1469-72. doi: 10.1126/science.1108408. Epub 2005 Apr 7.
5
Dense core vesicle dynamics in Caenorhabditis elegans neurons and the role of kinesin UNC-104.秀丽隐杆线虫神经元中致密核心囊泡的动态变化及驱动蛋白UNC-104的作用
Traffic. 2004 Jul;5(7):544-59. doi: 10.1111/j.1600-0854.2004.00195.x.
6
Fast vesicle transport in PC12 neurites: velocities and forces.PC12神经突中的快速囊泡运输:速度与力
Eur Biophys J. 2004 Nov;33(7):623-32. doi: 10.1007/s00249-004-0403-6. Epub 2004 Apr 8.
7
Cargo-carrying motor vehicles on the neuronal highway: transport pathways and neurodegenerative disease.神经元高速公路上的载货机动车辆:运输途径与神经退行性疾病
J Neurobiol. 2004 Feb 5;58(2):258-71. doi: 10.1002/neu.10319.
8
Molecular motors.分子马达
Nature. 2003 Apr 17;422(6933):759-65. doi: 10.1038/nature01601.
9
The molecular motor toolbox for intracellular transport.用于细胞内运输的分子马达工具箱。
Cell. 2003 Feb 21;112(4):467-80. doi: 10.1016/s0092-8674(03)00111-9.
10
Bcl-2 rescues motoneurons from early cell death in the cervical spinal cord of the chicken embryo.Bcl-2可挽救鸡胚颈脊髓运动神经元的早期细胞死亡。
J Neurobiol. 2002 Nov 15;53(3):381-90. doi: 10.1002/neu.10108.

每个囊泡中活性运动蛋白较少可能解释了雏鸡运动神经元在体外培养三天后囊泡运输减慢的现象。

Fewer active motors per vesicle may explain slowed vesicle transport in chick motoneurons after three days in vitro.

作者信息

Macosko Jed C, Newbern Jason M, Rockford Jean, Chisena Ernest N, Brown Charlotte M, Holzwarth George M, Milligan Carol E

机构信息

Department of Physics, Wake Forest University, Winston-Salem, NC 27109, USA.

出版信息

Brain Res. 2008 May 23;1211:6-12. doi: 10.1016/j.brainres.2008.03.014. Epub 2008 Mar 20.

DOI:10.1016/j.brainres.2008.03.014
PMID:18433736
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2464625/
Abstract

Vesicle transport in cultured chick motoneurons was studied over a period of 3 days using motion-enhanced differential interference contrast (MEDIC) microscopy, an improved version of video-enhanced DIC. After 3 days in vitro (DIV), the average vesicle velocity was about 30% less than after 1 DIV. In observations at 1, 2 and 3 DIV, larger vesicles moved more slowly than small vesicles, and retrograde vesicles were larger than anterograde vesicles. The number of retrograde vesicles increased relative to anterograde vesicles after 3 DIV, but this fact alone could not explain the decrease in velocity, since the slowing of vesicle transport in maturing motoneurons was observed independently for both anterograde and retrograde vesicles. In order to better understand the slowing trend, the distance vs. time trajectories of individual vesicles were examined at a frame rate of 8.3/s. Qualitatively, these trajectories consisted of short (1-2 s) segments of constant velocity, and the changes in velocity between segments were abrupt (<0.2 s). The trajectories were therefore fit to a series of connected straight lines. Surprisingly, the slopes of theses lines, i.e. the vesicle velocities, were often found to be multiples of ~0.6 mum/s. The velocity histogram showed multiple peaks, which, when fit with Gaussians using a least squares minimization, yielded an average spacing of 0.57 mum/s (taken as the slope of a fit to peak position vs. peak number, R(2)=0.994). We propose that the abrupt velocity changes occur when 1 or 2 motors suddenly begin or cease actively participating in vesicle transport. Under this hypothesis, the decrease in average vesicle velocity observed for maturing motoneurons is due to a decrease in the average number of active motors per vesicle.

摘要

利用运动增强型微分干涉对比(MEDIC)显微镜(视频增强型微分干涉对比的改进版本),对培养的鸡运动神经元中的囊泡运输进行了为期3天的研究。体外培养3天(DIV)后,囊泡的平均速度比培养1天后降低了约30%。在1、2和3 DIV时的观察发现,较大的囊泡比较小的囊泡移动得更慢,逆行囊泡比顺行囊泡更大。3 DIV后,逆行囊泡的数量相对于顺行囊泡有所增加,但仅这一事实并不能解释速度的下降,因为在成熟运动神经元中,顺行和逆行囊泡的运输速度均出现了独立下降。为了更好地理解这种速度下降趋势,以8.3帧/秒的帧率检查了单个囊泡的距离与时间轨迹。定性地说,这些轨迹由短(1-2秒)的匀速段组成,各段之间的速度变化是突然的(<0.2秒)。因此,这些轨迹拟合为一系列相连直线。令人惊讶的是,这些直线的斜率,即囊泡速度,通常是~0.6μm/s的倍数。速度直方图显示有多个峰值,使用最小二乘法最小化拟合高斯曲线时,平均间距为0.57μm/s(作为拟合峰值位置与峰值数量的斜率,R(2)=0.994)。我们提出,当1个或2个马达突然开始或停止积极参与囊泡运输时,就会发生速度的突然变化。在这一假设下,成熟运动神经元中观察到的囊泡平均速度下降是由于每个囊泡中活跃马达的平均数量减少所致。