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1
Experimental modification of PC12 neurite shape with the microtubule-depolymerizing drug Nocodazole: a serial electron microscopic study of neurite shape control.用微管解聚药物诺考达唑对PC12神经突形状进行实验性改变:神经突形状控制的系列电子显微镜研究
J Cell Biol. 1986 Sep;103(3):907-15. doi: 10.1083/jcb.103.3.907.
2
Changes in the organization of the neuritic cytoskeleton during nerve growth factor-activated differentiation of PC12 cells: a serial electron microscopic study of the development and control of neurite shape.神经生长因子激活PC12细胞分化过程中神经突细胞骨架组织的变化:神经突形态发育与调控的系列电子显微镜研究
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3
The cytoskeleton of neurites after microtubule depolymerization.微管解聚后神经突的细胞骨架。
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4
Tension and compression in the cytoskeleton of PC-12 neurites. II: Quantitative measurements.PC-12神经突细胞骨架中的张力和压缩。II:定量测量。
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Intracellular control of axial shape in non-uniform neurites: a serial electron microscopic analysis of organelles and microtubules in AI and AII retinal amacrine neurites.非均匀神经突中轴形状的细胞内控制:对AI和AII视网膜无长突神经突中细胞器和微管的系列电子显微镜分析
J Cell Biol. 1984 Apr;98(4):1279-90. doi: 10.1083/jcb.98.4.1279.
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Sequential phosphorylation of chartin microtubule-associated proteins is regulated by the presence of microtubules.Chartin微管相关蛋白的顺序磷酸化受微管存在的调节。
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Cell. 1980 Sep;21(2):333-8. doi: 10.1016/0092-8674(80)90469-9.

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Tension and compression in the cytoskeleton of PC-12 neurites. II: Quantitative measurements.PC-12神经突细胞骨架中的张力和压缩。II:定量测量。
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9
PC12 cells express juvenile microtubule-associated proteins during nerve growth factor-induced neurite outgrowth.在神经生长因子诱导的神经突生长过程中,PC12细胞表达幼年微管相关蛋白。
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Cold stable microtubules in brain studied in fractions and slices.在分离组分和切片中研究大脑中的冷稳定微管。
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Neuroblastoma cells recapitulate their detailed neurite morphologies after reversible microtubule disassembly.神经母细胞瘤细胞在微管可逆性解体后可重现其详细的神经突形态。
Cell. 1980 Sep;21(2):333-8. doi: 10.1016/0092-8674(80)90469-9.
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Changes in composition and activity of microtubule-associated proteins during brain development.脑发育过程中微管相关蛋白的组成与活性变化
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A biochemical model for neurite outgrowth during brain development.
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Calcium lability of cytoplasmic microtubules and its modulation by microtubule-associated proteins.细胞质微管的钙敏感性及其由微管相关蛋白介导的调节作用
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Serial reconstruction of microtubular arrays within dendrites of the cat retinal ganglion cell: the cytoskeleton of a vertebrate dendrite.猫视网膜神经节细胞树突内微管阵列的连续重建:脊椎动物树突的细胞骨架
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Intracellular control of axial shape in non-uniform neurites: a serial electron microscopic analysis of organelles and microtubules in AI and AII retinal amacrine neurites.非均匀神经突中轴形状的细胞内控制:对AI和AII视网膜无长突神经突中细胞器和微管的系列电子显微镜分析
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Axonal tubulin and axonal microtubules: biochemical evidence for cold stability.轴突微管蛋白与轴突微管:冷稳定性的生化证据。
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用微管解聚药物诺考达唑对PC12神经突形状进行实验性改变:神经突形状控制的系列电子显微镜研究

Experimental modification of PC12 neurite shape with the microtubule-depolymerizing drug Nocodazole: a serial electron microscopic study of neurite shape control.

作者信息

Jacobs J R, Stevens J K

出版信息

J Cell Biol. 1986 Sep;103(3):907-15. doi: 10.1083/jcb.103.3.907.

DOI:10.1083/jcb.103.3.907
PMID:3745274
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2114310/
Abstract

The microtubule-depolymerizing drug Nocodazole has been used to experimentally manipulate the form of PC12 neurites. Both time-lapse photography and serial electron microscopy demonstrate that microtubule depolymerization leads to varicosity formation due to a clustering of membranous organelles in young neurites (nerve growth factor activated within 7 d). Neurites that have been nerve growth factor activated 7 or more d before Nocodazole application are resistant to microtubule depolymerization. These data and data from previous papers has been combined in an attempt to predict quantitatively the volume and the shape of a neurite. The relationship is described mathematically by Vn = 4.52 Vo + 0.0054 MTl, where Vn is local neurite volume, Vo is organelle volume, and MTl is MT length (the constant, 0.0054 is micron2), and 4.52 is the obligatory volume constant derived from serial electron microscopic studies. The equation predicts the total volume of neurites despite alterations of morphology due to Nocodazole and despite changes in morphology during development.

摘要

微管解聚药物诺考达唑已被用于实验性地操控PC12神经突的形态。延时摄影和连续电子显微镜观察均表明,微管解聚会导致幼龄神经突(在7天内被神经生长因子激活)中膜性细胞器聚集,从而形成膨体。在应用诺考达唑之前7天或更长时间已被神经生长因子激活的神经突对微管解聚具有抗性。这些数据与之前论文中的数据相结合,试图定量预测神经突的体积和形状。这种关系通过数学公式Vn = 4.52 Vo + 0.0054 MTl来描述,其中Vn是局部神经突体积,Vo是细胞器体积,MTl是微管长度(常数0.0054的单位是平方微米),4.52是源自连续电子显微镜研究的必需体积常数。该方程能够预测神经突的总体积,尽管诺考达唑会导致形态改变,且发育过程中形态也会发生变化。