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1
Suppression of vinculin expression by antisense transfection confers changes in cell morphology, motility, and anchorage-dependent growth of 3T3 cells.通过反义转染抑制纽蛋白表达可导致3T3细胞的细胞形态、运动能力及锚定依赖性生长发生改变。
J Cell Biol. 1993 Sep;122(6):1285-94. doi: 10.1083/jcb.122.6.1285.
2
Modulation of alpha-actinin levels affects cell motility and confers tumorigenicity on 3T3 cells.α-辅肌动蛋白水平的调节会影响细胞运动,并赋予3T3细胞致瘤性。
J Cell Sci. 1994 Jul;107 ( Pt 7):1773-82. doi: 10.1242/jcs.107.7.1773.
3
Suppression of tumorigenicity in transformed cells after transfection with vinculin cDNA.用纽蛋白cDNA转染后转化细胞致瘤性的抑制。
J Cell Biol. 1992 Oct;119(2):427-38. doi: 10.1083/jcb.119.2.427.
4
Effects of antisense glial fibrillary acidic protein complementary DNA on the growth, invasion, and adhesion of human astrocytoma cells.反义胶质纤维酸性蛋白互补DNA对人星形细胞瘤细胞生长、侵袭及黏附的影响
Cancer Res. 1994 Jun 15;54(12):3267-72.
5
Reexpression of the major protein kinase C substrate, SSeCKS, suppresses v-src-induced morphological transformation and tumorigenesis.主要蛋白激酶C底物SSeCKS的重新表达可抑制v-src诱导的形态转化和肿瘤发生。
Cancer Res. 1997 Jun 1;57(11):2304-12.
6
Overexpression of vinculin suppresses cell motility in BALB/c 3T3 cells.纽蛋白的过表达抑制BALB/c 3T3细胞的运动能力。
Cell Motil Cytoskeleton. 1992;22(2):127-34. doi: 10.1002/cm.970220206.
7
Overexpression of the Na(+)/K(+)/Cl(-) cotransporter gene induces cell proliferation and phenotypic transformation in mouse fibroblasts.钠/钾/氯协同转运蛋白基因的过表达诱导小鼠成纤维细胞的细胞增殖和表型转化。
J Cell Physiol. 2000 Jan;182(1):109-18. doi: 10.1002/(SICI)1097-4652(200001)182:1<109::AID-JCP12>3.0.CO;2-A.
8
NIH 3T3 cells stably transfected with the gene encoding phosphatidylcholine-hydrolyzing phospholipase C from Bacillus cereus acquire a transformed phenotype.用编码蜡样芽孢杆菌磷脂酰胆碱水解磷脂酶C的基因稳定转染的NIH 3T3细胞获得了转化表型。
Mol Cell Biol. 1994 Jan;14(1):646-54. doi: 10.1128/mcb.14.1.646-654.1994.
9
Increased growth of NIH/3T3 cells by transfection with human p120 complementary DNA and inhibition by a p120 antisense construct.通过转染人p120互补DNA增加NIH/3T3细胞的生长,并被p120反义构建体抑制。
Cancer Res. 1992 Jan 15;52(2):428-36.
10
Transient induction of vinculin gene expression in 3T3 fibroblasts stimulated by serum-growth factors.血清生长因子刺激下3T3成纤维细胞中纽蛋白基因表达的瞬时诱导。
Cell Regul. 1990 Aug;1(9):621-36. doi: 10.1091/mbc.1.9.621.

引用本文的文献

1
Osteocytic vinculin controls bone mass by modulating Mef2c-driven sclerostin expression in mice.骨细胞中的纽蛋白通过调节小鼠中由Mef2c驱动的硬化蛋白表达来控制骨量。
Bone Res. 2025 Aug 13;13(1):73. doi: 10.1038/s41413-025-00452-x.
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Vinculin-Arp2/3 interaction inhibits branched actin assembly to control migration and proliferation. vinculin-Arp2/3 相互作用抑制分支状肌动蛋白组装以控制迁移和增殖。
Life Sci Alliance. 2024 Nov 15;8(2). doi: 10.26508/lsa.202402583. Print 2025 Feb.
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Dietary Polyphenols Effects on Focal Adhesion Plaques and Metalloproteinases in Cancer Invasiveness.膳食多酚对癌症侵袭中粘着斑和金属蛋白酶的影响。
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5
First body of evidence suggesting a role of a tankyrase-binding motif (TBM) of vinculin (VCL) in epithelial cells.首个证据表明纽蛋白(VCL)的端锚聚合酶结合基序(TBM)在上皮细胞中发挥作用。
PeerJ. 2021 May 27;9:e11442. doi: 10.7717/peerj.11442. eCollection 2021.
6
The role of extracellular matrix stiffness in regulating cytoskeletal remodeling via vinculin in synthetic smooth muscle cells.细胞外基质硬度通过黏着斑蛋白调节合成平滑肌细胞中细胞骨架重构的作用。
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7
Processed eggshell membrane powder regulates cellular functions and increase MMP-activity important in early wound healing processes.加工蛋壳膜粉末可调节细胞功能,并增加在早期伤口愈合过程中重要的 MMP 活性。
PLoS One. 2018 Aug 6;13(8):e0201975. doi: 10.1371/journal.pone.0201975. eCollection 2018.
8
Vinculin in cell-cell and cell-matrix adhesions.纽蛋白在细胞间和细胞与基质黏附中的作用。
Cell Mol Life Sci. 2017 Aug;74(16):2999-3009. doi: 10.1007/s00018-017-2511-3. Epub 2017 Apr 11.
9
Mechanisms and Functions of Vinculin Interactions with Phospholipids at Cell Adhesion Sites.纽蛋白在细胞黏附位点与磷脂相互作用的机制及功能
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10
The Intricate Interplay between Mechanisms Underlying Aging and Cancer.衰老与癌症潜在机制之间的复杂相互作用。
Aging Dis. 2014 Feb 16;6(1):56-75. doi: 10.14336/AD.2014.0209. eCollection 2015 Feb.

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Ruffling and locomotion: role in cell resistance to growth factor-induced proliferation.膜 ruffling 与细胞运动:在细胞对生长因子诱导增殖的抗性中的作用
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Signal transduction from the extracellular matrix.来自细胞外基质的信号转导。
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Suppression of tumorigenicity in simian virus 40-transformed 3T3 cells transfected with alpha-actinin cDNA.用α-辅肌动蛋白cDNA转染的猿猴病毒40转化的3T3细胞中致瘤性的抑制
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Vinculin: a cytoskeletal target of the transforming protein of Rous sarcoma virus.纽蛋白:劳氏肉瘤病毒转化蛋白的细胞骨架靶点。
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Progressive loss of shape-responsive metabolic controls in cells with increasingly transformed phenotype.随着细胞表型逐渐转变,其对形状反应性代谢控制的渐进性丧失。
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Protein synthesis requires cell-surface contact while nuclear events respond to cell shape in anchorage-dependent fibroblasts.蛋白质合成需要细胞表面接触,而在锚定依赖性成纤维细胞中,核内事件对细胞形状有反应。
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通过反义转染抑制纽蛋白表达可导致3T3细胞的细胞形态、运动能力及锚定依赖性生长发生改变。

Suppression of vinculin expression by antisense transfection confers changes in cell morphology, motility, and anchorage-dependent growth of 3T3 cells.

作者信息

Rodríguez Fernández J L, Geiger B, Salomon D, Ben-Ze'ev A

机构信息

Department of Molecular Genetics and Virology, Weizmann Institute of Science, Rehovot, Israel.

出版信息

J Cell Biol. 1993 Sep;122(6):1285-94. doi: 10.1083/jcb.122.6.1285.

DOI:10.1083/jcb.122.6.1285
PMID:8376463
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2119864/
Abstract

The expression of vinculin, a major component of adhesion plaques and cell-cell junctions, is markedly modulated in cells during growth activation, differentiation, motility and cell transformation. The stimulation of quiescent cells by serum factors and the culturing of cells on highly adhesive matrices induce vinculin gene expression, whereas the transformation of fibroblast and epithelial cells often results in decreased vinculin expression (reviewed in Rodríguez Fernández, J. L., B. Geiger, D. Salomon, I. Sabanay, M. Zöller, and A. Ben-Ze'ev. 1992. J. Cell Biol. 119:427). To study the effect of reduced vinculin expression on cell behavior, 3T3 cells were transfected with an antisense vinculin cDNA construct, and clones displaying decreased vinculin levels down to 10-30% of control levels were isolated. These cells showed a round phenotype with smaller and fewer vinculin-positive plaques localized mostly at the cell periphery. In addition, they displayed an increased motility compared to controls, manifested by a faster closure of "wounds" introduced into the monolayer, and by the formation of longer phagokinetic tracks. Moreover, the antisense transfectants acquired a higher cloning efficiency and produced larger colonies in soft agar than the parental counterparts. The results demonstrate that the regulation of vinculin expression in cells can affect, in a major way, cell shape and motility, and that decreased vinculin expression can induce cellular changes reminiscent of those found in transformed cells.

摘要

纽蛋白是黏着斑和细胞间连接的主要成分,在细胞生长激活、分化、运动及细胞转化过程中,其表达受到显著调节。血清因子刺激静止细胞以及将细胞培养在高黏附性基质上可诱导纽蛋白基因表达,而成纤维细胞和上皮细胞的转化通常会导致纽蛋白表达降低(见 Rodríguez Fernández, J. L., B. Geiger, D. Salomon, I. Sabanay, M. Zöller, and A. Ben-Ze'ev. 1992. J. Cell Biol. 119:427中的综述)。为研究纽蛋白表达降低对细胞行为的影响,用反义纽蛋白cDNA构建体转染3T3细胞,并分离出纽蛋白水平降至对照水平的10% - 30%的克隆。这些细胞呈现圆形表型,纽蛋白阳性斑更小且数量更少,大多位于细胞周边。此外,与对照相比,它们的运动性增强,表现为单层中引入的“伤口”愈合更快,以及形成更长的吞噬运动轨迹。而且,反义转染细胞比亲代细胞获得了更高的克隆效率,在软琼脂中形成更大的集落。结果表明,细胞中纽蛋白表达的调节可在很大程度上影响细胞形状和运动性,纽蛋白表达降低可诱导类似于转化细胞中发现的细胞变化。