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对《结蛋白和波形蛋白表达增加通过JNK2降低膀胱平滑肌收缩力》的修正

Correction to "Increased expression of desmin and vimentin reduces bladder smooth muscle contractility via JNK2".

出版信息

FASEB J. 2024 Dec 15;38(23):e70219. doi: 10.1096/fj.202402902.

Abstract

Javed E, Thangavel C, Frara N, et al. Increased expression of desmin and vimentin reduces bladder smooth muscle contractility via JNK2. The FASEB Journal. 2020;34:2126-2146. https://doi.org/10.1096/fj.201901301R The authors report that in Figure 2C and Figure 2D, identical bands are shown for GFP and GAPDH as these protein bands were obtained from the same experiment. The authors revised Figure 2C and Figure 2D using GFP and GAPDH bands from different experiments to avoid confusion. In addition, in Figure 2C, the bands labeled as GFP and GAPDH were misidentified while making the figure. This mistake has been corrected. The same GFP panel was used in Figures 6 and 7 because it was the control for desmin and vimentin overexpression. The figure legends have been corrected to make this clarification. In Figure 8, murine bladder smooth muscle (BSM) strips overexpressing GFP, or desmin, or vimentin were immunoblotted with antibodies against pJNK and GAPDH. BSM strips expressing GFP served as the control. The membrane was developed with short (Panel A) and long (Panel B) exposure times. The correct bands for pJNK and GAPDH were taken from the membrane with long-exposure time from GFP and vimentin (Figure 8E). However, the authors mistakenly included the bands for pJNK and GAPDH from the membrane with short exposure in Figure 8C from GFP and vimentin, instead of the intended bands from GFP and desmin. Figure 8C should have the pJNK and GAPDH bands from GFP and desmin. This error occurred due to the strong similarity between the pJNK bands in GFP/desmin and GFP/vimentin, as well as the GAPDH bands in GFP/desmin and GFP/vimentin. In the corrected Figure 8C, the bands for pJNK and GAPDH are included from GFP and desmin blots. The pJNK and GAPDH bands could come from different exposure times because they are from the same experiment. These errors do not change the results or conclusions of the article. The authors apologize for these errors. The corrected Figure 2 is as follows: FIGURE 2. Adenovirus-mediated overexpression of vimentin in murine BSM strips. (A) Schematic depiction of vimentin-GFP bicistronic adenoviral vector construct. (B) Schematic depiction of GFP adenoviral vector construct. (C, D) Murine BSM strips devoid of urothelium, and submucosa were transduced with an adenovirus encoding GFP and vimentin for 48 h and the expression levels of vimentin, desmin, and GFP proteins were determined by immunoblot analysis. GAPDH was used as a loading control. (E, F) Quantification of immunoblot data. (G) Sections prepared from murine BSM strips overexpressing vimentin and GFP proteins were stained with anti-vimentin, anti-SM22, and Alexa Fluor 488-labeled GFP antibody, followed by Cy3 and Cy5 conjugated secondary antibodies. Representative confocal images are shown. Scale bars = 10 μm. (H) Quantification of confocal images data. Data are expressed as means ± SD (E, F, and H), n = 5 mice in each group (E, F, and H). **p < .01 versus GFP-expressing murine BSM strips. FIGURE 6. Effect of desmin overexpression on smooth muscle marker proteins' expression in murine BSM. (A) Murine BSM strips devoid of urothelium, and submucosa were transduced with an adenovirus encoding GFP and desmin for 48 h and the expression levels of SMA and SM22 were determined by immunoblot analysis. GAPDH was used as a loading control. (B) Quantification of immunoblot data. (C, D) Sections prepared from murine BSM strips overexpressing desmin and GFP proteins were stained with anti-SMA, or anti-SM22, or anti-SMHC or Alexa Fluor 488-labeled GFP antibody, followed by Cy3 and Cy5 conjugated secondary antibodies. Representative confocal images are shown in (C) and (D); Scale bars = 50 μm. € Quantification of confocal images data. Data are expressed as means ± SD, n = 5 mice in each group. NS indicates nonsignificant. Note that the same GFP panel was used in Figures 6 and 7 because it was the control for both desmin and vimentin overexpression. FIGURE 7. Effect of vimentin overexpression on smooth muscle marker proteins' expression in murine BSM. (A) Murine BSM strips devoid of urothelium, and submucosa were transduced with an adenovirus encoding GFP and vimentin for 48 h and the expression levels of SMA, and SM22 were determined by immunoblot analysis. GAPDH was used as a loading control. (B) Quantification of immunoblot data. (C, D) Sections prepared from murine BSM strips overexpressing vimentin and GFP proteins were stained with anti-SMA, or anti- SM22, or anti-SMHC or Alexa Fluor 488-labeled GFP antibody, followed by Cy3 and Cy5 conjugated secondary antibodies. Representative confocal images are shown in C and D, Scale bars = 50 μm. (E) Quantification of confocal images data. Data are expressed as means ± SD, n = 5 mice in each group. NS indicates nonsignificant. Note that the same GFP panel was used in Figures 6 and 7 because it was the control for both desmin and vimentin overexpression. The corrected Figure 8 is as follows: FIGURE 8. Desmin and vimentin interact with JNK2 and enhance the phospho JNK level following the IF protein overexpression in murine BSM. (A, B) Murine BSM strips devoid of urothelium, and submucosa were transduced with an adenovirus encoding GFP, desmin and vimentin for 48 h and the total proteins from GFP, desmin and vimentin overexpressing murine BSM strips were immunoprecipitated with JNK2 antibody. The resulting immunoprecipitate was separated on a SDS-PAGE and subsequently probed with either anti-desmin and anti-JNK2 antibodies (A) or anti-vimentin and anti-JNK2 antibodies (B). The input served as a loading control in both (A) and (B). (C-F) Increased levels of phospho JNK following desmin and vimentin overexpression. Total proteins extracted from GFP, desmin and vimentin overexpressing murine BSM strips were subjected to immunoblot analysis using phosphorylated JNK and total JNK2 antibodies. GAPDH was used as a loading control. (D, F) Quantification of immunoblots (C, E). Data are expressed as means ± SD, n = 5 mice in each group. **p < .01 versus GFP expressing murine BSM strips.

摘要

贾韦德·E、坦加维尔·C、弗拉拉·N等。结蛋白和波形蛋白表达增加通过JNK2降低膀胱平滑肌收缩力。《美国实验生物学会联合会杂志》。2020年;34:2126 - 2146。https://doi.org/10.1096/fj.201901301R 作者报告称,在图2C和图2D中,GFP和GAPDH显示出相同的条带,因为这些蛋白条带是从同一实验中获得的。作者使用来自不同实验的GFP和GAPDH条带对图2C和图2D进行了修订,以避免混淆。此外,在图2C中,标记为GFP和GAPDH的条带在制作图时被误认。此错误已得到纠正。图6和图7中使用了相同的GFP图版,因为它是结蛋白和波形蛋白过表达的对照。图注已作修正以作此说明。在图8中,用抗pJNK和GAPDH抗体对过表达GFP、结蛋白或波形蛋白的小鼠膀胱平滑肌(BSM)条进行免疫印迹分析。表达GFP 的BSM条用作对照。膜分别用短曝光时间(图A)和长曝光时间(图B)显影。pJNK和GAPDH的正确条带取自GFP和波形蛋白长曝光时间的膜(图8E)。然而,作者错误地在图8C中包含了来自GFP和波形蛋白短曝光膜的pJNK和GAPDH条带,而不是预期的来自GFP和结蛋白的条带。图8C应该有来自GFP和结蛋白的pJNK和GAPDH条带。由于GFP/结蛋白和GFP/波形蛋白中pJNK条带以及GFP/结蛋白和GFP/波形蛋白中GAPDH条带非常相似,所以出现了这个错误。在修正后的图8C中,包含了来自GFP和结蛋白印迹的pJNK和GAPDH条带。pJNK和GAPDH条带可能来自不同的曝光时间,因为它们来自同一实验。这些错误不会改变文章的结果或结论。作者对这些错误表示歉意。修正后的图如下:图2. 腺病毒介导波形蛋白在小鼠BSM条中的过表达。(A)波形蛋白 - GFP双顺反子腺病毒载体构建体的示意图。(B)GFP腺病毒载体构建体的示意图。(C、D)用编码GFP和波形蛋白的腺病毒转导去除尿路上皮和黏膜下层的小鼠BSM条48小时,通过免疫印迹分析测定波形蛋白、结蛋白和GFP蛋白的表达水平。GAPDH用作上样对照。(E、F)免疫印迹数据的定量分析。(G)用抗波形蛋白、抗SM22和Alexa Fluor 488标记的GFP抗体对过表达波形蛋白和GFP蛋白的小鼠BSM条制备的切片进行染色,然后用Cy3和Cy5偶联的二抗进行染色。显示代表性共聚焦图像。比例尺 = 10μm。(H)共聚焦图像数据的定量分析。数据表示为平均值 ± 标准差(E、F和H),每组n = 5只小鼠(E、F和H)。**与表达GFP的小鼠BSM条相比,p < 0.01。图6. 结蛋白过表达对小鼠BSM中平滑肌标志物蛋白表达的影响。(A)用编码GFP和结蛋白的腺病毒转导去除尿路上皮和黏膜下层的小鼠BSM条48小时,通过免疫印迹分析测定SMA和SM22的表达水平。GAPDH用作上样对照。(B)免疫印迹数据的定量分析。(C、D)用抗SMA、抗SM22、抗SMHC或Alexa Fluor 488标记的GFP抗体对过表达结蛋白和GFP蛋白的小鼠BSM条制备的切片进行染色,然后用Cy3和Cy5偶联的二抗进行染色。(C)和(D)中显示代表性共聚焦图像;比例尺 = 50μm。(E)共聚焦图像数据定量分析。数据表示为平均值 ± 标准差,每组n = 5只小鼠。NS表示无显著性差异。注意,图6和图7中使用了相同的GFP图版,因为它是结蛋白和波形蛋白过表达的对照。图7. 波形蛋白过表达对小鼠BSM中平滑肌标志物蛋白表达的影响。(A)用编码GFP和波形蛋白的腺病毒转导去除尿路上皮和黏膜下层的小鼠BSM条48小时,通过免疫印迹分析测定SMA和SM22的表达水平。GAPDH用作上样对照。(B)免疫印迹数据的定量分析。(C、D)用抗SMA、抗SM22、抗SMHC或Alexa Fluor 488标记的GFP抗体对过表达波形蛋白和GFP蛋白的小鼠BSM条制备的切片进行染色,然后用Cy3和Cy5偶联的二抗进行染色。C和D中显示代表性共聚焦图像,比例尺 = 50μm。(E)共聚焦图像数据的定量分析。数据表示为平均值 ± 标准差,每组n = 5只小鼠。NS表示无显著性差异。注意,图6和图7中使用了相同的GFP图版,因为它是结蛋白和波形蛋白过表达的对照。修正后的图8如下:图8. 结蛋白和波形蛋白与JNK2相互作用并在小鼠BSM中过表达IF蛋白后增强磷酸化JNK水平。(A、B)用编码GFP、结蛋白和波形蛋白的腺病毒转导去除尿路上皮和黏膜下层的小鼠BSM条48小时,用JNK2抗体对过表达GFP、结蛋白和波形蛋白的小鼠BSM条的总蛋白进行免疫沉淀。将所得免疫沉淀物在SDS - PAGE上分离,随后用抗结蛋白和抗JNK2抗体(A)或抗波形蛋白和抗JNK2抗体(B)进行检测。输入物在(A)和(B)中均用作上样对照。(C - F)结蛋白和波形蛋白过表达后磷酸化JNK水平升高。用磷酸化JNK和总JNK2抗体对从小鼠过表达GFP、结蛋白和波形蛋白的BSM条中提取的总蛋白进行免疫印迹分析。GAPDH用作上样对照。(D、F)免疫印迹(C、E)的定量分析。数据表示为平均值 ± 标准差,每组n = 5只小鼠。**与表达GFP的小鼠BSM条相比,p < 0.01。

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