Literature DB >> 28771711

Tannic acid attenuates TGF-β1-induced epithelial-to-mesenchymal transition by effectively intervening TGF-β signaling in lung epithelial cells.

Dhamotharan Pattarayan1, Ayyanar Sivanantham1, Venkateshwaran Krishnaswami2, Lakshmanan Loganathan3, Rajaguru Palanichamy1, Subramanian Natesan2, Karthikeyan Muthusamy3, Subbiah Rajasekaran1.   

Abstract

Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive, and an irreversible lung disorder characterized by the accumulation of fibroblasts and myofibroblasts in the extracellular matrix. The transforming growth factor-β1 (TGF-β1)-induced epithelial-to-mesenchymal transition (EMT) is thought to be one of the possible sources for a substantial increase in the number of fibroblasts/myofibroblasts in IPF lungs. Tannic acid (TA), a natural dietary polyphenolic compound has been shown to possess diverse pharmacological effects. However, whether TA can inhibit TGF-β1-mediated EMT in lung epithelial cells remains enigmatic. Both the human adenocarcinomic alveolar epithelial (A549) and normal bronchial epithelial (BEAS-2B) cells were treated with TGF-β1 with or without TA. Results showed that TA addition, markedly inhibited TGF-β1-induced EMT as assessed by reduced expression of N-cadherin, type-1-collagen, fibronectin, and vimentin. Furthermore, TA inhibited TGF-β1-induced cell proliferation through inducing cell cycle arrest at G0/G1 phase. TGF-β1-induced increase in the phosphorylation of Smad (Smad2 and 3), Akt as well as that of mitogen activated protein kinase (ERK1/2, JNK1/2, and p38) mediators was effectively inhibited by TA. On the other hand, TA reduced the TGF-β1-induced increase in TGF-β receptors expression. Using molecular docking approach, FTIR, HPLC and Western blot analyses, we further identified the direct binding of TA to TGF-β1. Finally, we conclude that TA might directly interact with TGF-β1, thereby repressing TGF-β signaling and subsequent EMT process in lung epithelial cells. Further animal studies are needed to clarify its potential therapeutic benefit in pulmonary fibrosis.
© 2017 Wiley Periodicals, Inc.

Entities:  

Keywords:  EMT; TGF-β signaling; Tannic acid; cell proliferation; pulmonary fibrosis

Mesh:

Substances:

Year:  2017        PMID: 28771711     DOI: 10.1002/jcp.26127

Source DB:  PubMed          Journal:  J Cell Physiol        ISSN: 0021-9541            Impact factor:   6.384


  17 in total

1.  Tannic acid prevents macrophage-induced pro-fibrotic response in lung epithelial cells via suppressing TLR4-mediated macrophage polarization.

Authors:  Ayyanar Sivanantham; Dhamotharan Pattarayan; Nandhine Rajasekar; Adithi Kannan; Lakshmanan Loganathan; Ramalingam Bethunaickan; Santanu Kar Mahapatra; Rajaguru Palanichamy; Karthikeyan Muthusamy; Subbiah Rajasekaran
Journal:  Inflamm Res       Date:  2019-09-05       Impact factor: 4.575

2.  Fetal bovine serum induces sustained, but reversible, epithelial-mesenchymal transition in the BEAS-2B cell line.

Authors:  S W Malm; E A Amouzougan; W T Klimecki
Journal:  Toxicol In Vitro       Date:  2018-04-17       Impact factor: 3.500

3.  Polyphenol-Conjugated Bimetallic Au@AgNPs for Improved Wound Healing.

Authors:  Piotr Orlowski; Magdalena Zmigrodzka; Emilia Tomaszewska; Katarzyna Ranoszek-Soliwoda; Beata Pajak; Anna Slonska; Joanna Cymerys; Grzegorz Celichowski; Jaroslaw Grobelny; Malgorzata Krzyzowska
Journal:  Int J Nanomedicine       Date:  2020-07-13

4.  Effects of the isothiocyanate sulforaphane on TGF-β1-induced rat cardiac fibroblast activation and extracellular matrix interactions.

Authors:  Charity Fix; Amanda Carver-Molina; Mrinmay Chakrabarti; Mohamad Azhar; Wayne Carver
Journal:  J Cell Physiol       Date:  2019-01-04       Impact factor: 6.384

5.  Tannic acid alleviates experimental pulmonary fibrosis in mice by inhibiting inflammatory response and fibrotic process.

Authors:  Nandhine Rajasekar; Ayyanar Sivanantham; Amrita Kar; Santanu Kar Mahapatra; Rajesh Ahirwar; Rajesh K Thimmulappa; Sudhakar Gandhi Paramasivam; Rajasekaran Subbiah
Journal:  Inflammopharmacology       Date:  2020-05-05       Impact factor: 4.473

6.  Rapamycin Protects Against Peritendinous Fibrosis Through Activation of Autophagy.

Authors:  Wei Zheng; Yun Qian; Shuai Chen; Hongjiang Ruan; Cunyi Fan
Journal:  Front Pharmacol       Date:  2018-04-20       Impact factor: 5.810

Review 7.  Epithelial mesenchymal transition (EMT): a universal process in lung diseases with implications for cystic fibrosis pathophysiology.

Authors:  Nathan Rout-Pitt; Nigel Farrow; David Parsons; Martin Donnelley
Journal:  Respir Res       Date:  2018-07-18

Review 8.  Natural Plants Compounds as Modulators of Epithelial-to-Mesenchymal Transition.

Authors:  Lorena Avila-Carrasco; Pedro Majano; José Antonio Sánchez-Toméro; Rafael Selgas; Manuel López-Cabrera; Abelardo Aguilera; Guadalupe González Mateo
Journal:  Front Pharmacol       Date:  2019-07-30       Impact factor: 5.810

9.  Effects of emodin, a plant-derived anthraquinone, on TGF-β1-induced cardiac fibroblast activation and function.

Authors:  Wayne Carver; Ethan Fix; Charity Fix; Daping Fan; Mrinmay Chakrabarti; Mohamad Azhar
Journal:  J Cell Physiol       Date:  2021-05-27       Impact factor: 6.513

10.  Dual role of RACK1 in airway epithelial mesenchymal transition and apoptosis.

Authors:  Yue Pu; Yuan-Qi Liu; Yan Zhou; Yi-Fan Qi; Shi-Ping Liao; Shi-Kun Miao; Li-Ming Zhou; Li-Hong Wan
Journal:  J Cell Mol Med       Date:  2020-02-17       Impact factor: 5.310

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