Correction to "Genetic and pharmacological inhibition of GITR-GITRL interaction reduces chronic lung injury induced by bleomycin instillation".

IF 4.4 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
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引用次数: 0

Abstract

Cuzzocrea, S., Ronchetti, S., Genovese, T., Mazzon, E., Agostini, M., Di Paola, R., Esposito, E., Muià, C., Nocentini, G. and Riccardi, C. (2007), Genetic and pharmacological inhibition of GITR-GITRL interaction reduces chronic lung injury induced by bleomycin instillation. The FASEB Journal, 21: 117-129. https://doi.org/10.1096/fj.06-6611com The authors report that while preparing Figure 10B, the beta-tubulin image was placed incorrectly; specifically, it was flipped horizontally. Due to the time that has passed, the original data are no longer available to correct the image. The figure legend has been corrected to clarify that the same beta-tubulin image was used in Figures 10A and 10B because the blots shown are from the same experiment and beta-tubulin is the experimental control. The error does not change the results or conclusions of the article. FIGURE 10 Effect of genetic or pharmacological inhibition of GITR-GITRL interaction on NF-κB activation in lungs following bleomycin administration. A basal level of IK B-e was detected in the lung tissues from sham-treated GITR+/+ and GITR-/-mice (A, Aa), whereas in 7 d bleomycin-treated GITR+/+ mice IκB-α levels were substantially reduced (A, Aa). A significant prevention of IκB-é degradation induced by bleomycin instillation was observed in the lung tissues collected from GITR-/- mice (A, Aa). Western blot with β-tubulin was performed to verify that equivalent amounts of proteins were loaded in each lane. *p ~ .05 vs. sham; °p ~ .05 vs. bleomycin-treated GITR+/+ mice. In addition, bleomycin instillation caused a significant increase in the phosphorylation of Ser-536 in the lung tissues from GITR+/+ mice (B, Ba). A significant reduction of the phosphorylation of p65 on Ser-536 was observed in the lung tissues from GITR-/- mice (B, Ba). Western blot with β-tubulin was performed to verify that equivalent amounts of proteins were loaded in each lane. *p < .01 vs. sham; °p < .01 vs. bleomycin-treated -GITR+/+ mice. Moreover, the levels of the NF-κB p65 subunit protein in the nuclear fractions from lung tissue were also significantly increased after bleomycin instillation com compared to the sham-treated mice (C, Ca). A significant reduction of the NFκB p65 protein levels was observed in the tissues from GITR-/- mice (C, Ca). *p < .01 vs. sham; °p < .01 vs. bleomycin-treated GITR+/+ mice. Immunoblotting in (A-C) is representative of one blot out of five analyzed. The results in (Aa, Ba, and Ca) are expressed as mean ± se from five blots. The same blot for β-tubulin was used in panels (A) and (B) because it is from the same experiment.

对 "基因和药物抑制 GITR-GITRL 相互作用可减少博莱霉素灌注引起的慢性肺损伤 "的更正
Cuzzocrea, S., Ronchetti, S., Genovese, T., Mazzon, E., Agostini, M., Di Paola, R., Esposito, E., Muià, C., Nocentini, G. and Riccardi, C. (2007), Genetic and pharmacological inhibition of GITR-GITRL interaction reduces chronic lung injury induced by bleomycin instillation.The FASEB Journal, 21: 117-129. https://doi.org/10.1096/fj.06-6611com 作者报告说,在准备图 10B 时,β-微管蛋白图像的位置不正确;具体地说,它被水平翻转了。由于时间久远,原始数据已无法更正。图例已更正,以说明图 10A 和图 10B 使用了相同的 beta-微管蛋白图像,因为显示的印迹来自同一实验,而 beta-微管蛋白是实验对照。该错误不会改变文章的结果或结论。图 10 基因或药物抑制 GITR-GITRL 相互作用对博莱霉素给药后肺部 NF-κB 激活的影响。在假处理的 GITR+/+ 小鼠和 GITR-/ 小鼠的肺组织中检测到基础水平的 IK B-e(A,Aa),而在博莱霉素处理的 GITR+/+ 小鼠中,IκB-α 水平大幅降低(A,Aa)。在收集的 GITR-/- 小鼠肺组织中,观察到博莱霉素灌注诱导的 IκB-é 降解明显减少(A,Aa)。用 β-微管蛋白进行 Western 印迹,以验证各泳道中的蛋白质含量相等。*p ~ .05 vs. 假小鼠; °p ~ .05 vs. 博莱霉素处理的 GITR+/+ 小鼠。此外,博莱霉素灌注导致 GITR+/+ 小鼠肺组织中 Ser-536 磷酸化显著增加(B,Ba)。在 GITR-/- 小鼠的肺组织中观察到 p65 在 Ser-536 上的磷酸化明显减少(B,Ba)。用 β-微管蛋白进行 Western 印迹,以验证各泳道中的蛋白质含量相等。*p +/+ 小鼠。此外,与假治疗小鼠相比,博莱霉素灌注后小鼠肺组织核馏分中的 NF-κB p65 亚基蛋白水平也显著升高(C,Ca)。在 GITR-/- 小鼠组织中观察到 NFκB p65 蛋白水平明显降低(C,Ca)。*p +/+ 小鼠。A-C)中的免疫印迹是所分析的五张印迹中的一张。Aa、Ba 和 Ca)中的结果以五个印迹的平均值 ± se 表示。由于(A)和(B)板中使用的是同一实验中的β-微管蛋白印迹,因此(A)和(B)板中使用的是同一印迹。
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
The FASEB Journal
The FASEB Journal 生物-生化与分子生物学
CiteScore
9.20
自引率
2.10%
发文量
6243
审稿时长
3 months
期刊介绍: The FASEB Journal publishes international, transdisciplinary research covering all fields of biology at every level of organization: atomic, molecular, cell, tissue, organ, organismic and population. While the journal strives to include research that cuts across the biological sciences, it also considers submissions that lie within one field, but may have implications for other fields as well. The journal seeks to publish basic and translational research, but also welcomes reports of pre-clinical and early clinical research. In addition to research, review, and hypothesis submissions, The FASEB Journal also seeks perspectives, commentaries, book reviews, and similar content related to the life sciences in its Up Front section.
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