2007Journal of Jiangsu UniversityRequires access

Effect of activated JNK on pulmonary fibroblasts secretion matrix induced by TGF-β_1 in vitro

Zeng Yu

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Abstract

Objective: To investigate the effect of activated c-Jun NH2-terminal kinase(JNK)、P38 on pulmonary fibroblasts secretion matrix induced by transforming growth factor β1(TGF-β1).Methods: The human pulmonary fibroblasts cultured on plastic plates were divided into following groups: TGF-β1,TGF-β1+ SB203580,TGF-β1+DMSO,TGF-β1+ SB600125,Control.The expression of total JNK(T-JNK),phosphorylated JNK(p*-JNK),total P38(T-P38) and phosphorylated P38(p*P38) were assessed by Western blot,FN and LN were detected by Western blot. Results: A marked increase in p*-JNK was seen in pulmonary fibroblasts while the expression of p*-P38 had no obvious change after being induced by TGF-β1.Protein level of FN and LN was increased markedly at 48 hours after the treatment of TGF-β1.Addition of JNK inhibitor SB600125 largely abrogated the effect of TGF-β1. Conclusion: TGF-β1 can induce the secretion matrix of pulmonary fibroblasts via JNK signal pathway.

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Objective: To investigate the effect of activated c-Jun NH2-terminal kinase(JNK)、P38 on pulmonary fibroblasts secretion matrix induced by transforming growth factor β1(TGF-β1).Methods: The human pulmonary fibroblasts cultured on plastic plates were divided into following groups: TGF-β1,TGF-β1+ SB203580,TGF-β1+DMSO,TGF-β1+ SB600125,Control.The expression of total JNK(T-JNK),phosphorylated JNK(p*-JNK),total P38(T-P38) and phosphorylated P38(p*P38) were assessed by Western blot,FN and LN were detected by Western blot. Results: A marked increase in p*-JNK was seen in pulmonary fibroblasts while the expression of p*-P38 had no obvious change after being induced by TGF-β1.Protein level of FN and LN was increased markedly at 48 hours after the treatment of TGF-β1.Addition of JNK inhibitor SB600125 largely abrogated the effect of TGF-β1. Conclusion: TGF-β1 can induce the secretion matrix of pulmonary fibroblasts via JNK signal pathway.

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Available abstract

Objective: To investigate the effect of activated c-Jun NH2-terminal kinase(JNK)、P38 on pulmonary fibroblasts secretion matrix induced by transforming growth factor β1(TGF-β1).Methods: The human pulmonary fibroblasts cultured on plastic plates were divided into following groups: TGF-β1,TGF-β1+ SB203580,TGF-β1+DMSO,TGF-β1+ SB600125,Control.The expression of total JNK(T-JNK),phosphorylated JNK(p*-JNK),total P38(T-P38) and phosphorylated P38(p*P38) were assessed by Western blot,FN and LN were detected by Western blot. Results: A marked increase in p*-JNK was seen in pulmonary fibroblasts while the expression of p*-P38 had no obvious change after being induced by TGF-β1.Protein level of FN and LN was increased markedly at 48 hours after the treatment of TGF-β1.Addition of JNK inhibitor SB600125 largely abrogated the effect of TGF-β1. Conclusion: TGF-β1 can induce the secretion matrix of pulmonary fibroblasts via JNK signal pathway.

Key concepts: p38 mitogen-activated protein kinases, Transforming growth factor, Western blot, Secretion, Kinase, Phosphorylation, Pulmonary fibrosis, Molecular biology

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