更正“Versican V2异构体通过调节内皮细胞活性和纤维连接蛋白表达来促进血管生成”。

IF 3.5 4区 生物学 Q1 Biochemistry, Genetics and Molecular Biology
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引用次数: 0

摘要

杨伟宁,尔冬坚。Versican V2异构体通过调节内皮细胞活性和纤维连接蛋白表达促进血管生成。FEBS Letters 2013;587: 185 - 192。https://doi.org/10.1016/j.febslet.2012.11.023在已发表文章的图3B中,5x和20x两幅矢量图像是同一矢量样本共培养5天后的图像。4张V2图像(5x, 20x, 20x, 20x)为同一V2样本共培养5天后的图像。这是有意为之,通过多张图片向读者展示细胞间相互作用的更多细节。本勘误表的出版是为了修改图例,使这一点更清楚。修改后的图例如下所示。图3表达versican V2促进细胞间相互作用和管状结构的形成。(A) V2和载体转染的细胞与内皮细胞EOMA按1:1比例共培养。5天后,对共培养细胞拍照。与对照细胞相比,V2细胞显示出更高的与EOMA细胞相互作用的能力。结果表明,与对照细胞相比,V2细胞与EOMA细胞接触紧密;(B) V2和载体转染的细胞与YPEN内皮细胞按1:1的比例共培养。5天后,对共培养细胞拍照。这两个矢量图像是一个样本。四张V2图像(一张是5倍放大,另外三张是20倍放大)也是一个样本。YPEN细胞能与表达V2的U87细胞良好混合,但不能与对照细胞混合;(C) V2和载体转染的细胞与YPEN细胞混合,接种于Matrigel中,检查管形成情况。与V2细胞混合时,YPEN细胞形成复杂的管状结构,而与对照细胞混合时则不形成;(D)管状结构的典型照片;(E)将V2和载体转染的细胞与EOMA细胞混合进行管形成实验。同样,EOMA细胞与V2细胞混合时形成复杂的管状结构,而与对照细胞混合时则没有。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Correction to “Versican V2 isoform enhances angiogenesis by regulating endothelial cell activities and fibronectin expression”

Weining Yang, Albert J. Yee. Versican V2 isoform enhances angiogenesis by regulating endothelial cell activities and fibronectin expression. FEBS Letters 2013; 587: 185-192. https://doi.org/10.1016/j.febslet.2012.11.023

In Fig. 3B of the published article, the two vector images (5x and 20x) are of the same vector sample 5 days after co-culture. The four V2 images (5x, 20x, 20x, 20x) are of the same V2 sample 5 days after co-culture. This was intentional, with the multiple images included to show readers more detail of the cell–cell interaction. This corrigendum has been published to amend the figure legend to make this clear. The amended figure legend is shown below.

Figure 3

Expression versican V2 promotes cell–cell interaction and tube-like structure formation. (A) V2- and vector-transfected cells were co-cultured with endothelial cells EOMA at a 1:1 ratio. After 5 days, the co-cultured cells were photographed. The V2 cells displayed higher capacities in interaction with EOMA cells than the control cells. As a result, there was closed contact between the V2 and EOMA cells compared with the control cells; (B) V2- and vector-transfected cells were co-cultured with YPEN endothelial cells at a ratio of 1:1. After 5 days, the co-cultured cells were photographed. The two vector images are of a single sample. The four V2 images (one at 5x magnification, and the other three at 20x magnification) are also of a single sample. YPEN cells could mix well with V2 expressing U87 cells, but not the control cells; (C) V2- and vector-transfected cells were mixed with YPEN cells and inoculated in Matrigel, followed by examination of tube formation. The YPEN cells formed complex tube-like structures when mixed with the V2 cells, but not with the control cells; (D) typical photographs of tube-like structures are shown; (E) V2- and vector-transfected cells were mixed with EOMA cells for tube formation assay. Similarly, the EOMA cells formed complex tube-like structures when mixed with the V2 cells, but not with the control cells.

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来源期刊
FEBS Letters
FEBS Letters 生物-生化与分子生物学
CiteScore
7.00
自引率
2.90%
发文量
303
审稿时长
1.0 months
期刊介绍: FEBS Letters is one of the world''s leading journals in molecular biology and is renowned both for its quality of content and speed of production. Bringing together the most important developments in the molecular biosciences, FEBS Letters provides an international forum for Minireviews, Research Letters and Hypotheses that merit urgent publication.
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