Pivotal Role of TGF-β/Smad Signaling in Cardiac Fibrosis: Non-coding RNAs as Effectual Players

Unintended cardiac fibroblast proliferation in many pathophysiological heart conditions, known as cardiac fibrosis, results in pooling of extracellular matrix (ECM) proteins in the heart muscle. Transforming growth factor β (TGF-β) as a pivotal cytokine/growth factor stimulates fibroblasts and haste...

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Main Authors: Somayeh Saadat, Mahdi Noureddini, Maryam Mahjoubin-Tehran, Sina Nazemi, Layla Shojaie, Michael Aschner, Behnaz Maleki, Mohammad Abbasi-kolli, Hasan Rajabi Moghadam, Behrang Alani, Hamed Mirzaei
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-01-01
Series:Frontiers in Cardiovascular Medicine
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fcvm.2020.588347/full
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spelling doaj-518fd9fb6bda4710bbf170fb24642cf12021-01-25T04:58:54ZengFrontiers Media S.A.Frontiers in Cardiovascular Medicine2297-055X2021-01-01710.3389/fcvm.2020.588347588347Pivotal Role of TGF-β/Smad Signaling in Cardiac Fibrosis: Non-coding RNAs as Effectual PlayersSomayeh Saadat0Mahdi Noureddini1Maryam Mahjoubin-Tehran2Sina Nazemi3Layla Shojaie4Michael Aschner5Behnaz Maleki6Mohammad Abbasi-kolli7Hasan Rajabi Moghadam8Behrang Alani9Hamed Mirzaei10Physiology Research Centre, Kashan University of Medical Sciences, Kashan, IranPhysiology Research Centre, Kashan University of Medical Sciences, Kashan, IranDepartment of Medical Biotechnology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, IranVascular and Thorax Surgery Research Center, Shiraz University of Medical Sciences, Shiraz, IranDepartment of Medicine, Research Center for Liver Diseases, Keck School of Medicine, University of Southern California, Los Angeles, CA, United StatesDepartment of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, NY, United StatesPhysiology Research Centre, Kashan University of Medical Sciences, Kashan, IranDepartment of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, IranDepartment of Cardiology, Faculty of Medicine, Kashan University of Medical Sciences, Kashan, IranDepartment of Applied Cell Sciences, Faculty of Medicine, Kashan University of Medical Sciences, Kashan, IranResearch Center for Biochemistry and Nutrition in Metabolic Diseases, Institute for Basic Sciences, Kashan University of Medical Sciences, Kashan, IranUnintended cardiac fibroblast proliferation in many pathophysiological heart conditions, known as cardiac fibrosis, results in pooling of extracellular matrix (ECM) proteins in the heart muscle. Transforming growth factor β (TGF-β) as a pivotal cytokine/growth factor stimulates fibroblasts and hastens ECM production in injured tissues. The TGF-β receptor is a heterodimeric receptor complex on the plasma membrane, made up from TGF-β type I, as well as type II receptors, giving rise to Smad2 and Smad3 transcription factors phosphorylation upon canonical signaling. Phosphorylated Smad2, Smad3, and cytoplasmic Smad4 intercommunicate to transfer the signal to the nucleus, culminating in provoked gene transcription. Additionally, TGF-β receptor complex activation starts up non-canonical signaling that lead to the mitogen-stimulated protein kinase cascade activation, inducing p38, JNK1/2 (c-Jun NH2-terminal kinase 1/2), and ERK1/2 (extracellular signal–regulated kinase 1/2) signaling. TGF-β not only activates fibroblasts and stimulates them to differentiate into myofibroblasts, which produce ECM proteins, but also promotes fibroblast proliferation. Non-coding RNAs (ncRNAs) are important regulators of numerous pathways along with cellular procedures. MicroRNAs and circular long ncRNAs, combined with long ncRNAs, are capable of affecting TGF-β/Smad signaling, leading to cardiac fibrosis. More comprehensive knowledge based on these processes may bring about new diagnostic and therapeutic approaches for different cardiac disorders.https://www.frontiersin.org/articles/10.3389/fcvm.2020.588347/fullcardiac fibrosisnon-coding RNAsSmadTGF—transforming growth factormicroRNA
collection DOAJ
language English
format Article
sources DOAJ
author Somayeh Saadat
Mahdi Noureddini
Maryam Mahjoubin-Tehran
Sina Nazemi
Layla Shojaie
Michael Aschner
Behnaz Maleki
Mohammad Abbasi-kolli
Hasan Rajabi Moghadam
Behrang Alani
Hamed Mirzaei
spellingShingle Somayeh Saadat
Mahdi Noureddini
Maryam Mahjoubin-Tehran
Sina Nazemi
Layla Shojaie
Michael Aschner
Behnaz Maleki
Mohammad Abbasi-kolli
Hasan Rajabi Moghadam
Behrang Alani
Hamed Mirzaei
Pivotal Role of TGF-β/Smad Signaling in Cardiac Fibrosis: Non-coding RNAs as Effectual Players
Frontiers in Cardiovascular Medicine
cardiac fibrosis
non-coding RNAs
Smad
TGF—transforming growth factor
microRNA
author_facet Somayeh Saadat
Mahdi Noureddini
Maryam Mahjoubin-Tehran
Sina Nazemi
Layla Shojaie
Michael Aschner
Behnaz Maleki
Mohammad Abbasi-kolli
Hasan Rajabi Moghadam
Behrang Alani
Hamed Mirzaei
author_sort Somayeh Saadat
title Pivotal Role of TGF-β/Smad Signaling in Cardiac Fibrosis: Non-coding RNAs as Effectual Players
title_short Pivotal Role of TGF-β/Smad Signaling in Cardiac Fibrosis: Non-coding RNAs as Effectual Players
title_full Pivotal Role of TGF-β/Smad Signaling in Cardiac Fibrosis: Non-coding RNAs as Effectual Players
title_fullStr Pivotal Role of TGF-β/Smad Signaling in Cardiac Fibrosis: Non-coding RNAs as Effectual Players
title_full_unstemmed Pivotal Role of TGF-β/Smad Signaling in Cardiac Fibrosis: Non-coding RNAs as Effectual Players
title_sort pivotal role of tgf-β/smad signaling in cardiac fibrosis: non-coding rnas as effectual players
publisher Frontiers Media S.A.
series Frontiers in Cardiovascular Medicine
issn 2297-055X
publishDate 2021-01-01
description Unintended cardiac fibroblast proliferation in many pathophysiological heart conditions, known as cardiac fibrosis, results in pooling of extracellular matrix (ECM) proteins in the heart muscle. Transforming growth factor β (TGF-β) as a pivotal cytokine/growth factor stimulates fibroblasts and hastens ECM production in injured tissues. The TGF-β receptor is a heterodimeric receptor complex on the plasma membrane, made up from TGF-β type I, as well as type II receptors, giving rise to Smad2 and Smad3 transcription factors phosphorylation upon canonical signaling. Phosphorylated Smad2, Smad3, and cytoplasmic Smad4 intercommunicate to transfer the signal to the nucleus, culminating in provoked gene transcription. Additionally, TGF-β receptor complex activation starts up non-canonical signaling that lead to the mitogen-stimulated protein kinase cascade activation, inducing p38, JNK1/2 (c-Jun NH2-terminal kinase 1/2), and ERK1/2 (extracellular signal–regulated kinase 1/2) signaling. TGF-β not only activates fibroblasts and stimulates them to differentiate into myofibroblasts, which produce ECM proteins, but also promotes fibroblast proliferation. Non-coding RNAs (ncRNAs) are important regulators of numerous pathways along with cellular procedures. MicroRNAs and circular long ncRNAs, combined with long ncRNAs, are capable of affecting TGF-β/Smad signaling, leading to cardiac fibrosis. More comprehensive knowledge based on these processes may bring about new diagnostic and therapeutic approaches for different cardiac disorders.
topic cardiac fibrosis
non-coding RNAs
Smad
TGF—transforming growth factor
microRNA
url https://www.frontiersin.org/articles/10.3389/fcvm.2020.588347/full
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