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Geometric control of cell migration.细胞迁移的几何控制
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2
Micropatterning as a tool to decipher cell morphogenesis and functions.微图案化作为解析细胞形态发生和功能的工具。
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Collective cell migration.集体细胞迁移。
Annu Rev Cell Dev Biol. 2009;25:407-29. doi: 10.1146/annurev.cellbio.042308.113231.
4
Classical cadherins control nucleus and centrosome position and cell polarity.经典钙黏蛋白控制细胞核和中心体的位置以及细胞极性。
J Cell Biol. 2009 Jun 1;185(5):779-86. doi: 10.1083/jcb.200812034.
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In migrating cells, the Golgi complex and the position of the centrosome depend on geometrical constraints of the substratum.在迁移细胞中,高尔基体复合体和中心体的位置取决于基质的几何限制。
J Cell Sci. 2008 Jul 15;121(Pt 14):2406-14. doi: 10.1242/jcs.026849. Epub 2008 Jun 24.
6
Anisotropy of cell adhesive microenvironment governs cell internal organization and orientation of polarity.细胞黏附微环境的各向异性决定细胞内部组织和极性方向。
Proc Natl Acad Sci U S A. 2006 Dec 26;103(52):19771-6. doi: 10.1073/pnas.0609267103. Epub 2006 Dec 18.
7
A parallel-gradient microfluidic chamber for quantitative analysis of breast cancer cell chemotaxis.一种用于乳腺癌细胞趋化性定量分析的平行梯度微流控腔室。
Biomed Microdevices. 2006 Jun;8(2):109-18. doi: 10.1007/s10544-006-7706-6.
8
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.
9
Cell polarization mechanisms during directed cell migration.定向细胞迁移过程中的细胞极化机制。
Nat Cell Biol. 2005 Apr;7(4):336-7. doi: 10.1038/ncb0405-336.
10
Directing cell migration with asymmetric micropatterns.利用不对称微图案引导细胞迁移。
Proc Natl Acad Sci U S A. 2005 Jan 25;102(4):975-8. doi: 10.1073/pnas.0408954102. Epub 2005 Jan 14.

芯片上研究几何约束和化学梯度对细胞极性的影响。

An on-chip study on the influence of geometrical confinement and chemical gradient on cell polarity.

机构信息

Beijing Engineering Research Center for BioNanotechnology and CAS Key Laboratory for Biological Effects of Nanomaterials and Nanosafety, National Center for NanoScience and Technology , 11 BeiYiTiao, ZhongGuanCun, Beijing 100190, China.

Ecole Normale Superieure , 24 rue Lhomond, Paris, France.

出版信息

Biomicrofluidics. 2014 Oct 15;8(5):052010. doi: 10.1063/1.4898209. eCollection 2014 Sep.

DOI:10.1063/1.4898209
PMID:25538801
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4222261/
Abstract

Cell polarity plays key roles in tissue development, regeneration, and pathological processes. However, how the cells establish and maintain polarity is still obscure so far. In this study, by employing microfluidic techniques, we explored the influence of geometrical confinement and chemical stimulation on the cell polarity and their interplay. We found that teardrop shape-induced anterior/posterior polarization of cells displayed homogeneous distribution of epidermal growth factor receptor, and the polarity could be maintained in a uniform epidermal growth factor (EGF) solution, but be broken by a reverse gradient of EGF, implying different mechanism of geometrical and chemical cue-induced cell polarity. Further studies indicated that a teardrop pattern could cause polarized distribution of microtubule-organization center and nucleus-Golgi complex, and this polarity was weakened when the cells were released from the confinement. Our study provides the evidence regarding the difference between geometrical and chemical cue-induced cell polarity and would be useful for understanding relationship between polarity and directional migration of cells.

摘要

细胞极性在组织发育、再生和病理过程中起着关键作用。然而,迄今为止,细胞如何建立和维持极性仍然不清楚。在这项研究中,我们通过采用微流控技术,探索了几何约束和化学刺激对细胞极性的影响及其相互作用。我们发现,泪滴形状诱导的细胞前后极性表现出表皮生长因子受体的均匀分布,并且在均匀的表皮生长因子(EGF)溶液中可以维持这种极性,但在 EGF 的反向梯度中会被打破,这表明几何和化学线索诱导的细胞极性的机制不同。进一步的研究表明,泪滴图案会导致微管组织中心和核-高尔基复合体的极化分布,当细胞从约束中释放出来时,这种极性会减弱。我们的研究提供了关于几何和化学线索诱导的细胞极性之间差异的证据,这对于理解极性和细胞定向迁移之间的关系将是有用的。