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本文引用的文献

1
Oriented collagen fibers direct tumor cell intravasation.定向排列的胶原纤维引导肿瘤细胞进入血管。
Proc Natl Acad Sci U S A. 2016 Oct 4;113(40):11208-11213. doi: 10.1073/pnas.1610347113. Epub 2016 Sep 23.
2
Engineering Three-dimensional Epithelial Tissues Embedded within Extracellular Matrix.构建嵌入细胞外基质的三维上皮组织。
J Vis Exp. 2016 Jul 10(113):54283. doi: 10.3791/54283.
3
Swelling of Collagen-Hyaluronic Acid Co-Gels: An In Vitro Residual Stress Model.胶原蛋白-透明质酸共凝胶的肿胀:一种体外残余应力模型。
Ann Biomed Eng. 2016 Oct;44(10):2984-2993. doi: 10.1007/s10439-016-1636-0. Epub 2016 May 5.
4
Interstitial fluid pressure regulates collective invasion in engineered human breast tumors via Snail, vimentin, and E-cadherin.间质液压力通过Snail、波形蛋白和E-钙黏蛋白调节工程化人乳腺肿瘤中的集体侵袭。
Integr Biol (Camb). 2016 Mar 14;8(3):319-31. doi: 10.1039/c5ib00282f.
5
Collective cell migration in development.发育过程中的集体细胞迁移。
J Cell Biol. 2016 Jan 18;212(2):143-55. doi: 10.1083/jcb.201508047.
6
Dynamic tensile forces drive collective cell migration through three-dimensional extracellular matrices.动态拉伸力驱动细胞通过三维细胞外基质进行集体迁移。
Sci Rep. 2015 Jul 13;5:11458. doi: 10.1038/srep11458.
7
RalB regulates contractility-driven cancer dissemination upon TGFβ stimulation via the RhoGEF GEF-H1.在转化生长因子β(TGFβ)刺激下,RalB通过Rho鸟嘌呤核苷酸交换因子(RhoGEF)GEF-H1调节由收缩性驱动的癌症播散。
Sci Rep. 2015 Jul 8;5:11759. doi: 10.1038/srep11759.
8
E-cadherin junctions as active mechanical integrators in tissue dynamics.E-钙黏蛋白连接作为组织动态中的活性机械整合子。
Nat Cell Biol. 2015 May;17(5):533-9. doi: 10.1038/ncb3136.
9
Long-range force transmission in fibrous matrices enabled by tension-driven alignment of fibers.通过纤维的张力驱动排列实现纤维基质中的长程力传递。
Biophys J. 2014 Dec 2;107(11):2592-603. doi: 10.1016/j.bpj.2014.09.044.
10
3D collagen alignment limits protrusions to enhance breast cancer cell persistence.三维胶原蛋白排列限制突起以增强乳腺癌细胞的持久性。
Biophys J. 2014 Dec 2;107(11):2546-58. doi: 10.1016/j.bpj.2014.10.035.

纤维状细胞外基质的组织诱导排列动力学

Dynamics of Tissue-Induced Alignment of Fibrous Extracellular Matrix.

作者信息

Piotrowski-Daspit Alexandra S, Nerger Bryan A, Wolf Abraham E, Sundaresan Sankaran, Nelson Celeste M

机构信息

Department of Chemical and Biological Engineering, Princeton University, Princeton, New Jersey.

Department of Chemical and Biological Engineering, Princeton University, Princeton, New Jersey; Department of Molecular Biology, Princeton University, Princeton, New Jersey.

出版信息

Biophys J. 2017 Aug 8;113(3):702-713. doi: 10.1016/j.bpj.2017.06.046.

DOI:10.1016/j.bpj.2017.06.046
PMID:28793224
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5550306/
Abstract

Aligned fibers of extracellular matrix (ECM) affect the direction, efficiency, and persistence of migrating cells. To uncover the mechanisms by which multicellular tissues align their surrounding ECM before migration, we used an engineered three-dimensional culture model to investigate the dynamics of ECM alignment around tissues of defined geometry. Analysis of ECM alignment over time revealed that tissues rapidly reorganize their surrounding matrix, with a characteristic time that depends on the type of cell and the initial tissue geometry. We found that matrix metalloproteinase activity is not required for matrix alignment before cell migration. Instead, alignment is driven by Rho-mediated cytoskeletal contractility and accelerated by propagation of tension through intercellular adhesions. Our data suggest that multicellular tissues align their surrounding matrix by pulling collectively to exert strain, which is primarily a physical process. Consistently, the pattern of matrix alignment depends on tissue geometry and the resulting distribution of mechanical strain, with asymmetric tissues generating a higher degree of matrix alignment along their longest axes. The rapid ability of multicellular tissues to physically remodel their matrix enables their constituent cells to migrate efficiently along aligned fibers and to quickly change their direction according to other microenvironmental cues, which is important for both normal and disease processes.

摘要

细胞外基质(ECM)的排列纤维会影响迁移细胞的方向、效率和持久性。为了揭示多细胞组织在迁移前使其周围ECM排列的机制,我们使用了一种工程化的三维培养模型来研究特定几何形状组织周围ECM排列的动力学。对ECM随时间排列的分析表明,组织会迅速重组其周围的基质,其特征时间取决于细胞类型和初始组织几何形状。我们发现,在细胞迁移之前,基质金属蛋白酶活性对于基质排列并非必需。相反,排列是由Rho介导的细胞骨架收缩性驱动的,并通过细胞间粘附传递张力而加速。我们的数据表明,多细胞组织通过集体牵拉以施加应变来使其周围基质排列,这主要是一个物理过程。一致地,基质排列模式取决于组织几何形状以及由此产生的机械应变分布,不对称组织沿其最长轴产生更高程度的基质排列。多细胞组织快速物理重塑其基质的能力使其组成细胞能够沿着排列的纤维高效迁移,并根据其他微环境线索快速改变方向,这对于正常和疾病过程都很重要。