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Acta Pharmaceutica Sinica ; (12): 142-147, 2014.
Article in Chinese | WPRIM | ID: wpr-245088

ABSTRACT

This study is to investigate the effect of artesunate on transforming growth factor-beta1 (TGF-beta1) induced epithelial-mesenchymal transition (EMT) and its possible mechanism. After the in vitro cultured RLE-6TN cells were treated with TGF-beta1 then artesunate intervened on it, after 24 h, expression of the markers of mesenchymal cell was assayed using Western blotting and real-time PCR analysis. Western blotting was also used to detect the effect of TGF-beta1 on the Smad3 and Smad7 expressions of RLE-6TN cells. Morphological alterations were examined by phase-contrast microscope, and ultrastructure changes by electron microscope. Incubation of RLE-6TN cells with TGF-beta1 resulted in the up-regulation of the expression of the mesenchymal cell markers, after artesunate intervened on it, resulted in the down-regulation of the expression. Meanwhile, incubation with artesunate intervened on RLE-6TN cells could lead to the apparent down-regulation of the expression of Smad3 and up-regulation of Samd7 and the transition of RLE-6TN cells to mesenchymal-like by TGF-beta1 induction, after artesunate intervened on it, RLE-6TN cells to epithelial-like. TGF-beta1 induced epithelial-mesenchymal transition process; artesunate can inhibit TGF-beta1-induced epithelial-mesenchymal transition process, the possible mechanism is up-regulation of the expression of Smad7 and down-regulation of the expression of Smad3, meanwhile inhibits phosphorylation of Smad3.


Subject(s)
Animals , Rats , Actins , Genetics , Metabolism , Artemisia , Chemistry , Artemisinins , Pharmacology , Cell Line , Cell Proliferation , Epithelial Cells , Cell Biology , Metabolism , Epithelial-Mesenchymal Transition , Idiopathic Pulmonary Fibrosis , Pathology , Plants, Medicinal , Chemistry , Pulmonary Alveoli , Cell Biology , RNA, Messenger , Metabolism , Smad3 Protein , Genetics , Metabolism , Smad7 Protein , Genetics , Metabolism , Transforming Growth Factor beta1 , Pharmacology , Vimentin , Genetics , Metabolism
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