Fig 3.tif (943.5 kB)
Downregulation of LGR4 decreases ARPE-19 cell migration.
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posted on 2016-12-15, 19:08 authored by Qiang Hou, Linglin Zhou, Jiajia Tang, Nan Ma, Ancong Xu, Jiang Tang, Dandan Zheng, Xiaogang Chen, Feng Chen, Xiang Da Dong, LiLi TuARPE-19 cells were transfected with LGR4 specific siRNA or a scrambled negative control (NC). Transwell (A) and in vitro scratch assays (B) were performed to evaluate the ARPE-19 cell migration. The number of cells that migrated in the transwell assay was quantified by counting the number of cells appearing in the lower chamber in five independent vision fields with a 20X microscope objective. (C) For in vitro scratch assay, cells that migrated into the gap were counted at 48 hours and 72 hours as indicated. Results were expressed as mean ± SD (n = 3, *p < 0.05). All images are representative of at least three independent experiments. Scale bar: 100 μm for transwell assay, and 200 μm for in vitro scratch assay.
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ARPE -19 cell proliferationmiR -34a gene expression upregulationLGR 4 downregulation2FLGR 4 expressionLGR 4MicroRNA -34amigrationDouble luciferase gene reporter assayWestern blot analysisLGR 4 protein expressionmiR -34a involvementmiR -34a expression modulates changesprotein expression inhibitionmiR -34a upregulationmiR -34aRetinal Pigment Epithelial ARPE -19 CellsMTSpigment epithelial cell line ARPE -19.Ki 67 immunostainingCDK 6 protein expression
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