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首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >Erratum: Cathepsin K is involved in development of psoriasis-like skin lesions through TLR-dependent Th17 activation (Journal of Immunology (2013) 190 (4805-4811))
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Erratum: Cathepsin K is involved in development of psoriasis-like skin lesions through TLR-dependent Th17 activation (Journal of Immunology (2013) 190 (4805-4811))

机译:勘误:组织蛋白酶K通过TLR依赖的Th17激活参与牛皮癣样皮肤病变的发展(免疫学杂志(2013)190(4805-4811))

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摘要

Cathepsin K is involved in development of psoriasis-like skin lesions through TLR-dependent Thl7 activation. J. Immunol. 190: 4805-4811 There was an error in the data of Fig. 5 as published. Data shown in Fig. 5A as 1112a gene expression was duplicated from the data for 1123a. The correct data for 1112a gene expression is now shown in the revised Fig. 5 below. The figure legend was correct as published and is shown below for reference. This error does not change the conclusion of the paper.FIGURE 5. Effect of NC-2300 on IL-12 and IL-23 in bone marrow-derived mDCs after treatment of TLR7/8 ligands. (A) The mDCs were pretreated with vehicle alone or 10 |xM NC-2300 for 3 h prior to stimulation with 10 nM R848 for 24 h at 37°C. Treatment of R848-induced transcripts of III2a, III2b. and 1123a, all of which were inhibited by pretreatment with NC-2300. The data are shown as mean ± SD, *p < 0.05, **p < 0.01, ***p < 0.001, n = 6. Tukey test. (B) R848 was replaced with imiquimod (IMQ, 10 |xM) under the same experimental protocol. The results were mostly reproduced when IMQ was used. The data are shown as mean ± SD, **p < 0.01, ***p < 0.001, n = 6. Tukey test. (C) The mDCs were pretreated with vehicle alone or 1, 10, and 30 jjlM NC-2300 for 3 h prior to stimulation with 10 muM IMQ for 24 h at 37°C. The data represent mean ± SD, ###p < 0.001 versus vehicle-treated mDCs; *p < 0.05, **p < 0.01 versus IMQ-treated mDCs, n = 5. Tukey test.
机译:组织蛋白酶K通过TLR依赖的Th17激活参与牛皮癣样皮肤损伤的发展。 J.免疫。 190:4805-4811在发布的图5数据中存在错误。图5A中显示为1112a基因表达的数据与1123a的数据重复。现在,在下面的修订图5中显示了1112a基因表达的正确数据。该图例在发布时是正确的,下面显示以供参考。这个错误不会改变本文的结论。图5. NC-2300对TLR7 / 8配体处理后骨髓来源的mDC中IL-12和IL-23的影响。 (A)将mDC单独用赋形剂或10μMNC-2300预处理3 h​​,然后在37°C下用10 nM R848刺激24 h。 R848诱导的III2a,III2b转录本的处理。 1123a和1123a,所有这些都受到NC-2300预处理的抑制。数据显示为平均值±SD,* p <0.05,** p <0.01,*** p <0.001,n =6。图基检验。 (B)在相同的实验方案下,将R848替换为imiquimod(IMQ,10 | xM)。使用IMQ时,大多数结果都可以重现。数据显示为平均值±SD,** p <0.01,*** p <0.001,n =6。图基检验。 (C)在用10μMIMQ于37°C刺激24小时之前,先单独用媒介物,1、10和30 jlM NC-2300预处理mDC 3小时。数据表示相对于媒介物处理的mDC的平均值±SD,### p <0.001; * p <0.05,** p <0.01,相对于IMQ处理的mDC,n =5。Tukey测试。

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