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1
Taxol binds to cellular microtubules.紫杉醇与细胞微管结合。
J Cell Biol. 1982 Sep;94(3):688-96. doi: 10.1083/jcb.94.3.688.
2
Taxol binds to polymerized tubulin in vitro.紫杉醇在体外与聚合微管蛋白结合。
J Cell Biol. 1981 Nov;91(2 Pt 1):479-87. doi: 10.1083/jcb.91.2.479.
3
Direct photoaffinity labeling of tubulin with taxol.用紫杉醇对微管蛋白进行直接光亲和标记。
J Natl Cancer Inst. 1992 May 20;84(10):785-8. doi: 10.1093/jnci/84.10.785.
4
Taxol induces the formation of unusual arrays of cellular microtubules in colchicine-pretreated J774.2 cells.紫杉醇在经秋水仙碱预处理的J774.2细胞中诱导形成异常的细胞微管阵列。
Eur J Cell Biol. 1986 Oct;42(1):126-34.
5
Vinblastine paracrystals from cultured cells are calcium-stable.来自培养细胞的长春碱副晶体对钙稳定。
Exp Cell Res. 1984 Jan;150(1):205-12. doi: 10.1016/0014-4827(84)90715-8.
6
Taxol binds differentially to flagellar outer doublets and their reassembled microtubules.紫杉醇与鞭毛外双联微管及其重新组装的微管结合存在差异。
Cell Motil. 1983;3(2):123-30. doi: 10.1002/cm.970030203.
7
Taxol-requiring mutant of Chinese hamster ovary cells with impaired mitotic spindle assembly.需要紫杉醇的中国仓鼠卵巢细胞突变体,其有丝分裂纺锤体组装受损。
J Cell Biol. 1983 Jul;97(1):30-9. doi: 10.1083/jcb.97.1.30.
8
In vivo and in vitro studies on the role of HMW-MAPs in taxol-induced microtubule bundling.关于高分子量微管相关蛋白(HMW-MAPs)在紫杉醇诱导微管成束中作用的体内和体外研究。
Eur J Cell Biol. 1984 Jan;33(1):134-43.
9
(+)-Discodermolide binds to microtubules in stoichiometric ratio to tubulin dimers, blocks taxol binding and results in mitotic arrest.(+)-软海绵素以化学计量比与微管蛋白二聚体结合于微管,阻断紫杉醇结合并导致有丝分裂停滞。
Chem Biol. 1996 Apr;3(4):287-93. doi: 10.1016/s1074-5521(96)90108-8.
10
Rhazinilam mimics the cellular effects of taxol by different mechanisms of action.瑞扎尼拉姆通过不同的作用机制模拟紫杉醇的细胞效应。
Cell Motil Cytoskeleton. 1994;28(4):317-26. doi: 10.1002/cm.970280405.

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Low Intensity Ultrasound as an Antidote to Taxane/Paclitaxel-induced Cytotoxicity.低强度超声作为紫杉烷/紫杉醇诱导的细胞毒性的解毒剂
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本文引用的文献

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Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
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Plaque formation and isolation of pure lines with poliomyelitis viruses.脊髓灰质炎病毒的噬斑形成及纯系分离
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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。
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Cold and metabolic inhibitor effects on cytoplasmic microtubules and the Golgi complex in cultured rat epiphyseal chondrocytes.寒冷及代谢抑制剂对培养的大鼠骨骺软骨细胞中细胞质微管和高尔基体复合体的影响
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Molecular analysis of cytoplasmic microtubules in situ: identification of both widespread and specific proteins.原位细胞质微管的分子分析:广泛存在及特异性蛋白质的鉴定
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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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Stabilization and the cytoplasmic ground substance in detergent-opened cells and a structural and biochemical analysis of its composition.去污剂处理的开放细胞中的稳定作用与细胞质基质及其组成的结构和生化分析。
Proc Natl Acad Sci U S A. 1981 Jul;78(7):4329-33. doi: 10.1073/pnas.78.7.4329.
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ATP-dependent regulation of cytoplasmic microtubule disassembly.ATP依赖的细胞质微管拆卸调节
Proc Natl Acad Sci U S A. 1981 Jun;78(6):3610-3. doi: 10.1073/pnas.78.6.3610.
9
Phorbol myristate acetate stimulates microtubule and 10-nm filament extension and lysosome redistribution in mouse macrophages.佛波醇肉豆蔻酸酯乙酸盐刺激小鼠巨噬细胞中的微管和10纳米细丝伸展以及溶酶体重新分布。
J Cell Biol. 1980 Aug;86(2):641-55. doi: 10.1083/jcb.86.2.641.
10
Control of cell volume in the J774 macrophage by microtubule disassembly and cyclic AMP.通过微管拆卸和环磷酸腺苷对J774巨噬细胞中细胞体积的控制
J Cell Biol. 1981 Sep;90(3):761-8. doi: 10.1083/jcb.90.3.761.

紫杉醇与细胞微管结合。

Taxol binds to cellular microtubules.

作者信息

Manfredi J J, Parness J, Horwitz S B

出版信息

J Cell Biol. 1982 Sep;94(3):688-96. doi: 10.1083/jcb.94.3.688.

DOI:10.1083/jcb.94.3.688
PMID:6127342
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2112233/
Abstract

Taxol is a low molecular weight plant derivative which enhances microtubule assembly in vitro and has the unique ability to promote the formation of discrete microtubule bundles in cells. Tritium-labeled taxol binds directly to microtubules in vitro with a stoichiometry approaching one (Parness, J., and S. B. Horwitz, 1981, J. Cell Biol. 91:479-487). We now report studies in cells on the binding of [3H]taxol and the formation of microtubule bundles. [3H]Taxol binds to the macrophagelike cell line, J774.2, in a specific and saturable manner. Scatchard analysis of the specific binding data demonstrates a single set of high affinity binding sites. Maximal binding occurs at drug concentrations which produce maximal growth inhibition. Conditions which depolymerize microtubules in intact and extracted cells as determined by tubulin immunofluorescence inhibit the binding of [3H]taxol. This strongly suggests that taxol binds specifically to cellular microtubules. Extraction with 0.1% Nonidet P-40 or depletion of cellular ATP by treatment with 10 mM NaN3 prevents the characteristic taxol-induced bundle formation. The binding of [3H]taxol, however, is retained under these conditions. Thus, there formation. The binding of [3H]taxol, however, is retained under these conditions. Thus, there must be specific cellular mechanisms which are required for bundle formation, in addition to the direct binding of taxol to cytoplasmic microtubules.

摘要

紫杉醇是一种低分子量的植物衍生物,它在体外能增强微管组装,并且具有促进细胞中离散微管束形成的独特能力。氚标记的紫杉醇在体外以接近1的化学计量比直接与微管结合(帕尼斯,J.,和S. B. 霍维茨,1981,《细胞生物学杂志》91:479 - 487)。我们现在报告关于[³H]紫杉醇结合以及微管束形成的细胞研究。[³H]紫杉醇以特异性和可饱和的方式结合到巨噬细胞样细胞系J774.2上。对特异性结合数据的斯卡查德分析显示出一组单一的高亲和力结合位点。最大结合发生在产生最大生长抑制的药物浓度下。通过微管蛋白免疫荧光测定,能使完整细胞和提取细胞中的微管解聚的条件会抑制[³H]紫杉醇的结合。这有力地表明紫杉醇特异性地结合到细胞微管上。用0.1%的诺乃洗涤剂P - 40提取或用10 mM叠氮化钠处理使细胞ATP耗竭会阻止紫杉醇诱导的特征性束状结构形成。然而,在这些条件下[³H]紫杉醇的结合得以保留。因此,除了紫杉醇与细胞质微管的直接结合外,必定存在特定的细胞机制参与束状结构的形成。