Curcumin inhibits TGF-β1-induced phenotypic transition of human kidney tubular cells (HKCs)

Objective To study the effects of curcumine on renal tubular epithelial-mesenchymal transition (EMT) and its possible mechanisms. Methods The effect of curcumin on the morphology of human kidney cells (HKCs) in the presence of TGF-β1 alone or in combination with different concentration curcumine was...

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Main Author: CHEN Min-jia, DU Juan, YUAN Dan-feng, ZHANG Shu, HUANG Hong, ZHU Fang-qiang
Format: Article
Language:zho
Published: Institute of Basic Medical Sciences and Peking Union Medical College Hospital, Chinese Academy of Medical Sciences / Peking Union Medical College. 2020-01-01
Series:Jichu yixue yu linchuang
Subjects:
Online Access:http://journal11.magtechjournal.com/Jwk_jcyxylc/fileup/1001-6325/PDF/a190629.pdf
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author CHEN Min-jia, DU Juan, YUAN Dan-feng, ZHANG Shu, HUANG Hong, ZHU Fang-qiang
author_facet CHEN Min-jia, DU Juan, YUAN Dan-feng, ZHANG Shu, HUANG Hong, ZHU Fang-qiang
author_sort CHEN Min-jia, DU Juan, YUAN Dan-feng, ZHANG Shu, HUANG Hong, ZHU Fang-qiang
collection DOAJ
description Objective To study the effects of curcumine on renal tubular epithelial-mesenchymal transition (EMT) and its possible mechanisms. Methods The effect of curcumin on the morphology of human kidney cells (HKCs) in the presence of TGF-β1 alone or in combination with different concentration curcumine was observed by phase contrast microscopy. The expressions of E-cardhrin, keratin, vimentin, alpha smooth muscle actin (α-SMA),fibroblast-specific protein 1 (FSP1) and key proteins of AKT/mTOR pathway were analyzed by immunohistochemical stain and Western blot. Results HKC cells showed a classic cobblestone morphology. Exposure of HKCs to TGF-β1 for 72 h induced a complete conversion of the epithelial cell to myofibroblast. When HKCs were co-incubated with TGF-β1 and various concentrations of curcumin for 72 h, curcumine maintained the epithelial morphology in a dose-dependent manner (from 12.5 to 50 μg/mL), antagonizing TGF-β1-induced the down-regulation expression of E-cardhrin, keratin and the up-rgulation of FSP1, vimentin and α-SMA. Importantly. Curcumine effectively suppressed the activity of the Akt/mTOR pathway in HKCs as demonstrated by a remarkable reduction of the Akt, mTOR, p70S6K, 4E-BP1和eIF4E phosphorylation. Conclusions Curcumine is a potent inhibitor of TGF-β1-induced epithelial-mesenchymal transition (EMT) and antagonizes TGF-β1-driven fibrogenesis through inhibition of the activity of the Akt/mTOR pathway.
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spelling doaj.art-40c2586fca494b0db2104b8506666d8d2024-01-05T03:13:53ZzhoInstitute of Basic Medical Sciences and Peking Union Medical College Hospital, Chinese Academy of Medical Sciences / Peking Union Medical College.Jichu yixue yu linchuang1001-63252020-01-014014853Curcumin inhibits TGF-β1-induced phenotypic transition of human kidney tubular cells (HKCs)CHEN Min-jia, DU Juan, YUAN Dan-feng, ZHANG Shu, HUANG Hong, ZHU Fang-qiang01. State Key Laboratory of Trauma, Burn and Combined Injury, Daping Hospital, Army Medical University, Chongqing 400042;;2. Department of Urology, the Third Affiliated Hospital of Chongqing Medical University, Chongqing 401120, ChinaObjective To study the effects of curcumine on renal tubular epithelial-mesenchymal transition (EMT) and its possible mechanisms. Methods The effect of curcumin on the morphology of human kidney cells (HKCs) in the presence of TGF-β1 alone or in combination with different concentration curcumine was observed by phase contrast microscopy. The expressions of E-cardhrin, keratin, vimentin, alpha smooth muscle actin (α-SMA),fibroblast-specific protein 1 (FSP1) and key proteins of AKT/mTOR pathway were analyzed by immunohistochemical stain and Western blot. Results HKC cells showed a classic cobblestone morphology. Exposure of HKCs to TGF-β1 for 72 h induced a complete conversion of the epithelial cell to myofibroblast. When HKCs were co-incubated with TGF-β1 and various concentrations of curcumin for 72 h, curcumine maintained the epithelial morphology in a dose-dependent manner (from 12.5 to 50 μg/mL), antagonizing TGF-β1-induced the down-regulation expression of E-cardhrin, keratin and the up-rgulation of FSP1, vimentin and α-SMA. Importantly. Curcumine effectively suppressed the activity of the Akt/mTOR pathway in HKCs as demonstrated by a remarkable reduction of the Akt, mTOR, p70S6K, 4E-BP1和eIF4E phosphorylation. Conclusions Curcumine is a potent inhibitor of TGF-β1-induced epithelial-mesenchymal transition (EMT) and antagonizes TGF-β1-driven fibrogenesis through inhibition of the activity of the Akt/mTOR pathway.http://journal11.magtechjournal.com/Jwk_jcyxylc/fileup/1001-6325/PDF/a190629.pdfcurcumine|renal fibrosis|epithelialto-mesenchymal transition (emt)|tgf-β1|akt/mtor pathway
spellingShingle CHEN Min-jia, DU Juan, YUAN Dan-feng, ZHANG Shu, HUANG Hong, ZHU Fang-qiang
Curcumin inhibits TGF-β1-induced phenotypic transition of human kidney tubular cells (HKCs)
Jichu yixue yu linchuang
curcumine|renal fibrosis|epithelialto-mesenchymal transition (emt)|tgf-β1|akt/mtor pathway
title Curcumin inhibits TGF-β1-induced phenotypic transition of human kidney tubular cells (HKCs)
title_full Curcumin inhibits TGF-β1-induced phenotypic transition of human kidney tubular cells (HKCs)
title_fullStr Curcumin inhibits TGF-β1-induced phenotypic transition of human kidney tubular cells (HKCs)
title_full_unstemmed Curcumin inhibits TGF-β1-induced phenotypic transition of human kidney tubular cells (HKCs)
title_short Curcumin inhibits TGF-β1-induced phenotypic transition of human kidney tubular cells (HKCs)
title_sort curcumin inhibits tgf β1 induced phenotypic transition of human kidney tubular cells hkcs
topic curcumine|renal fibrosis|epithelialto-mesenchymal transition (emt)|tgf-β1|akt/mtor pathway
url http://journal11.magtechjournal.com/Jwk_jcyxylc/fileup/1001-6325/PDF/a190629.pdf
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