Erratum.

IF 2.2 4区 生物学 Q1 ANATOMY & MORPHOLOGY
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引用次数: 0

Abstract

In the article "Angiotensin II/Angiotensin II Receptor Blockade Affects Osteoporosis via the AT1/AT2-Mediated cAMP-Dependent PKA Pathway" [Cells Tissues Organs. 2017;204(1):25-37; https://doi.org/10.1159/000464461] by Yi Zhou et al., the authors noted there was an error in Figure 4c.Fig. 4.c Osteoclastic activity was estimated by TRAP staining. After completing osteoclast induction in the cell plate, cells were gently washed and fixed in 4% formaldehyde at room temperature for 30 s, followed by the TRAP staining procedure.An error in image naming and processing resulted in an incorrect image being placed in the fourth experimental group (AngII+ ARB1- ARB2+ group). The authors have verified the corrected image by checking laboratory records and timestamp of raw pictures. Due to the errors in labelling the first two images of each group, the authors have also replaced the blank control (AngII-; ARB1-; ARB2-) in Figure 4c.Detailed Protocol for TRAP StainingAlthough Figure 4c may visually suggest heterogeneity in staining among the groups, quantitative cell counting confirmed that the trends across groups were consistent and supported the conclusions of the article. The apparent visual differences are likely attributable to insufficient staining. The authors have outlined the contours of insufficiently stained cells with yellow dashed lines for clarity. Sample preparation was performed as follows: after completing osteoclast induction in the cell plate, the culture medium was discarded. The cell layer was gently washed with pre-warmed (37°C) PBS to prevent cell detachment. Cells were then fixed in 4% formaldehyde at room temperature for 30 s, followed by the TRAP staining procedure. Under light microscopy, TRAP-positive cells containing three or more nuclei were defined as multinucleated cells (MNCs).The corrected Figure 4c is shown here.

勘误表。
在文章“血管紧张素II/血管紧张素II受体阻断通过AT1/ at2介导的camp依赖性PKA途径影响骨质疏松症”[细胞组织器官,2017;204(1):25-37;通过Zhou Yi等人的https://doi.org/10.1159/000464461],作者注意到图4c中有一个错误。4.c通过TRAP染色估计破骨细胞活性。在细胞板中完成破骨细胞诱导后,将细胞轻轻洗涤,在4%甲醛中室温固定30 s,然后进行TRAP染色程序。由于图像命名和处理错误,导致错误的图像被放置在第四实验组(AngII+ ARB1- ARB2+组)。通过对实验记录和原始图片时间戳的核对,对校正后的图像进行了验证。由于每组前两幅图像标注错误,作者也替换了图4c中的空白对照(AngII-; ARB1-; ARB2-)。尽管图4c可能从视觉上显示各组间染色的异质性,但定量细胞计数证实各组间的趋势是一致的,并支持本文的结论。明显的视觉差异可能是由于染色不足造成的。为了清晰起见,作者用黄色虚线勾勒出染色不足的细胞的轮廓。样品制备方法如下:在细胞板中完成破骨细胞诱导后,丢弃培养基。用预热(37°C)的PBS轻轻清洗细胞层,以防止细胞脱落。然后将细胞在4%甲醛中室温固定30 s,然后进行TRAP染色程序。光镜下,含有三个或更多核的trap阳性细胞被定义为多核细胞(MNCs)。更正后的图4c显示在这里。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cells Tissues Organs
Cells Tissues Organs 生物-发育生物学
CiteScore
4.90
自引率
3.70%
发文量
45
审稿时长
6-12 weeks
期刊介绍: ''Cells Tissues Organs'' aims at bridging the gap between cell biology and developmental biology and the emerging fields of regenerative medicine (stem cell biology, tissue engineering, artificial organs, in vitro systems and transplantation biology). CTO offers a rapid and fair peer-review and exquisite reproduction quality. Special topic issues, entire issues of the journal devoted to a single research topic within the range of interests of the journal, are published at irregular intervals.
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