Literature DB >> 26659643

Correction: CTGF Increases IL-6 Expression in Human Synovial Fibroblasts through Integrin-Dependent Signaling Pathway.

Shan-Chi Liu, Chin-Jung Hsu, Hsien-Te Chen, Hsi-Kai Tsou, Show-Mei Chuang, Chih-Hsin Tang.   

Abstract

Entities:  

Year:  2015        PMID: 26659643      PMCID: PMC4686119          DOI: 10.1371/journal.pone.0144569

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


× No keyword cloud information.
The authors would like to correct Fig 3D, as errors were introduced in the preparation of this figure for publication. In Fig 3D, the left JNK panel appears as a duplicate of the right JNK panel. The authors have provided a corrected version of Fig 3 here.
Fig 3

JNK and p38 are involved in CTGF-mediated IL-6 production in synovial fibroblasts.

(A) OASFs were pretreated with SB203580, SP600125, U0126, and PD98059 for 30 min or transfected with p38 and JNK mutant for 24 h followed by stimulation with CTGF for 24 h. The IL-6 expression was examined by qPCR. (B) OASFs were pretreated with SB203580 and SP600125, for 30 min or transfected with p38 and JNK mutant for 24 h followed by stimulation with CTGF for 24 h. The IL-6 expression was examined by ELISA. (C) OASFs were incubated with CTGF for indicated time intervals, and JNK, p38, and ERK phosphorylation was examined by Western blotting. (D) OASFs were pretreated with αvβ5 integrin antibody (5 µg/ml) for 30 min or transfected with ASK1 shRNA for 24 h and then incubated with CTGF (10 ng/ml) for 30 min, and JNK, p38, and ERK phosphorylation was examined by Western blotting. *: p<0.05 as compared with basal level. #: p<0.05 as compared with CTGF-treated group.

The authors confirm that these changes do not alter their findings. The authors have provided raw, uncropped blots as Supporting Information.

JNK and p38 are involved in CTGF-mediated IL-6 production in synovial fibroblasts.

(A) OASFs were pretreated with SB203580, SP600125, U0126, and PD98059 for 30 min or transfected with p38 and JNK mutant for 24 h followed by stimulation with CTGF for 24 h. The IL-6 expression was examined by qPCR. (B) OASFs were pretreated with SB203580 and SP600125, for 30 min or transfected with p38 and JNK mutant for 24 h followed by stimulation with CTGF for 24 h. The IL-6 expression was examined by ELISA. (C) OASFs were incubated with CTGF for indicated time intervals, and JNK, p38, and ERK phosphorylation was examined by Western blotting. (D) OASFs were pretreated with αvβ5 integrin antibody (5 µg/ml) for 30 min or transfected with ASK1 shRNA for 24 h and then incubated with CTGF (10 ng/ml) for 30 min, and JNK, p38, and ERK phosphorylation was examined by Western blotting. *: p<0.05 as compared with basal level. #: p<0.05 as compared with CTGF-treated group.

Uncropped blots for Fig 3D.

(TIF) Click here for additional data file.
  1 in total

1.  CTGF increases IL-6 expression in human synovial fibroblasts through integrin-dependent signaling pathway.

Authors:  Shan-Chi Liu; Chin-Jung Hsu; Hsien-Te Chen; Hsi-Kai Tsou; Show-Mei Chuang; Chih-Hsin Tang
Journal:  PLoS One       Date:  2012-12-05       Impact factor: 3.240

  1 in total
  2 in total

1.  Epigenetic modifications of interleukin-6 in synovial fibroblasts from osteoarthritis patients.

Authors:  Fei Yang; Song Zhou; Chuandong Wang; Yan Huang; Huiwu Li; You Wang; Zhenan Zhu; Jian Tang; Mengning Yan
Journal:  Sci Rep       Date:  2017-03-06       Impact factor: 4.379

Review 2.  The pathogenic role of connective tissue growth factor in osteoarthritis.

Authors:  Min Tu; Yao Yao; Feng Hua Qiao; Li Wang
Journal:  Biosci Rep       Date:  2019-07-18       Impact factor: 3.840

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.