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本文引用的文献

1
The primary cilium as the cell's antenna: signaling at a sensory organelle.作为细胞天线的初级纤毛:在一种感觉细胞器上的信号传导
Science. 2006 Aug 4;313(5787):629-33. doi: 10.1126/science.1124534.
2
To stabilize neutrophil polarity, PIP3 and Cdc42 augment RhoA activity at the back as well as signals at the front.为稳定中性粒细胞极性,磷脂酰肌醇-3,4,5-三磷酸(PIP3)和Cdc42增强了细胞后部的RhoA活性以及前部的信号。
J Cell Biol. 2006 Jul 31;174(3):437-45. doi: 10.1083/jcb.200604113. Epub 2006 Jul 24.
3
Flies without centrioles.没有中心粒的苍蝇。
Cell. 2006 Jun 30;125(7):1375-86. doi: 10.1016/j.cell.2006.05.025.
4
Centrosome localization determines neuronal polarity.中心体定位决定神经元极性。
Nature. 2005 Aug 4;436(7051):704-8. doi: 10.1038/nature03811.
5
Polarity proteins in axon specification and synaptogenesis.轴突特化和突触形成中的极性蛋白。
Dev Cell. 2005 Jun;8(6):803-16. doi: 10.1016/j.devcel.2005.05.007.
6
Cdc42 controls the polarity of the actin and microtubule cytoskeletons through two distinct signal transduction pathways.Cdc42通过两条不同的信号转导途径控制肌动蛋白和微管细胞骨架的极性。
J Cell Sci. 2005 Jun 15;118(Pt 12):2579-87. doi: 10.1242/jcs.02385. Epub 2005 May 31.
7
Nuclear movement regulated by Cdc42, MRCK, myosin, and actin flow establishes MTOC polarization in migrating cells.由Cdc42、MRCK、肌球蛋白和肌动蛋白流调节的核运动在迁移细胞中建立了微管组织中心极化。
Cell. 2005 May 6;121(3):451-63. doi: 10.1016/j.cell.2005.02.022.
8
Neutrophil microtubules suppress polarity and enhance directional migration.中性粒细胞微管抑制极性并增强定向迁移。
Proc Natl Acad Sci U S A. 2005 May 10;102(19):6884-9. doi: 10.1073/pnas.0502106102. Epub 2005 Apr 28.
9
A physiological view of the primary cilium.初级纤毛的生理学观点。
Annu Rev Physiol. 2005;67:515-29. doi: 10.1146/annurev.physiol.67.040403.101353.
10
GSK-3beta regulates phosphorylation of CRMP-2 and neuronal polarity.糖原合成酶激酶-3β调节CRMP-2的磷酸化及神经元极性。
Cell. 2005 Jan 14;120(1):137-49. doi: 10.1016/j.cell.2004.11.012.

极性揭示了细胞内在的手性。

Polarity reveals intrinsic cell chirality.

作者信息

Xu Jingsong, Van Keymeulen Alexandra, Wakida Nicole M, Carlton Pete, Berns Michael W, Bourne Henry R

机构信息

Departments of Cellular and Molecular Pharmacology, School of Medicine, University of California-San Francisco, CA 94158, USA.

出版信息

Proc Natl Acad Sci U S A. 2007 May 29;104(22):9296-300. doi: 10.1073/pnas.0703153104. Epub 2007 May 17.

DOI:10.1073/pnas.0703153104
PMID:17517645
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1890488/
Abstract

Like blood neutrophils, dHL60 cells respond to a uniform concentration of attractant by polarizing in apparently random directions. How each cell chooses its own direction is unknown. We now find that an arrow drawn from the center of the nucleus of an unpolarized cell to its centrosome strongly predicts the subsequent direction of attractant-induced polarity: Of 60 cells that polarized in response to uniform f-Met-Leu-Phe (fMLP), 42 polarized to the left of this arrow, 6 polarized to the right, and 12 polarized directly toward or away from the centrosome. To investigate this directional bias we perturbed a regulatory pathway, downstream of Cdc42 and partitioning-defective 6 (Par6), which controls centrosome orientation relative to polarity of other cells. Dominant negative Par6 mutants block polarity altogether, as previously shown for disrupting Cdc42 activity. Cells remain able to polarize, but without directional bias, if their microtubules are disrupted with nocodazole, or they express mutant proteins that interfere with activities of PKCzeta or dynein. Expressing constitutively active glycogen synthase kinase 3beta (GSK3beta) causes cells to polarize preferentially to the right. Distributions of most of these polarity regulators localize to the centrosome but show no left-right asymmetry before polarization. Together, these findings suggest that an intrinsically chiral structure, perhaps the centrosome, serves as a template for directing polarity in the absence of spatial cues. Such a template could help to determine left-right asymmetry and planar polarity in development.

摘要

与血液中的中性粒细胞一样,dHL60细胞在均匀浓度的趋化因子作用下会向明显随机的方向极化。每个细胞如何选择自己的方向尚不清楚。我们现在发现,从未极化细胞的细胞核中心向其中心体绘制的箭头能强烈预测趋化因子诱导的极性的后续方向:在60个因均匀的f-甲硫氨酸-亮氨酸-苯丙氨酸(fMLP)而极化的细胞中,42个细胞向该箭头左侧极化,6个细胞向右侧极化,12个细胞直接向中心体或远离中心体极化。为了研究这种方向偏差,我们干扰了Cdc42和分区缺陷6(Par6)下游的一条调控通路,该通路控制中心体相对于其他细胞极性的方向。如先前所示,显性负性Par6突变体完全阻断极性,破坏Cdc42活性时也是如此。如果用诺考达唑破坏细胞的微管,或者它们表达干扰PKCzeta或动力蛋白活性的突变蛋白,细胞仍能极化,但没有方向偏差。组成型激活糖原合酶激酶3β(GSK3β)的表达会使细胞优先向右侧极化。这些极性调节因子中的大多数分布定位于中心体,但在极化前没有左右不对称性。这些发现共同表明,一种内在的手性结构,可能是中心体,在没有空间线索的情况下作为指导极性的模板。这样的模板可能有助于在发育过程中确定左右不对称性和平面极性。