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      Antagonistic effects of activin A and TNF-α on the activation of L929 fibroblast cells via Smad3-independent signaling

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          Abstract

          Fibroblasts play an important role in inflammation and tissue fibrosis. Both activin A and TNF-α can activate immune cells, however, the roles and relationship of them in activating fibroblasts in inflammation remain unclear. Here, this study revealed that TNF-α promoted the release of NO and IL-6 by L929 fibroblast cells, but co-treatment with activin A attenuated these effects. In contrast, activin A induced cell migration and increased the production of tissue fibrosis-related TGF-β1 and fibronectin, while TNF-α inhibited these function changes of L929 cells induced by activin A. Moreover, this study revealed that activin A and TNF-α regulated the activities of L929 cells via ERK1/2/MAPK pathway, rather than Smad3-dependent signaling pathway. Taken together, these data indicate that activin A and TNF-α exert mutually antagonistic effects on regulating fibroblasts activities, and the balance between their action may determine the process and outcome of fibroblasts-mediated inflammation.

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          Wound repair and regeneration: mechanisms, signaling, and translation.

          The cellular and molecular mechanisms underpinning tissue repair and its failure to heal are still poorly understood, and current therapies are limited. Poor wound healing after trauma, surgery, acute illness, or chronic disease conditions affects millions of people worldwide each year and is the consequence of poorly regulated elements of the healthy tissue repair response, including inflammation, angiogenesis, matrix deposition, and cell recruitment. Failure of one or several of these cellular processes is generally linked to an underlying clinical condition, such as vascular disease, diabetes, or aging, which are all frequently associated with healing pathologies. The search for clinical strategies that might improve the body's natural repair mechanisms will need to be based on a thorough understanding of the basic biology of repair and regeneration. In this review, we highlight emerging concepts in tissue regeneration and repair, and provide some perspectives on how to translate current knowledge into viable clinical approaches for treating patients with wound-healing pathologies.
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            The pathogenesis of cardiac fibrosis.

            Cardiac fibrosis is characterized by net accumulation of extracellular matrix proteins in the cardiac interstitium, and contributes to both systolic and diastolic dysfunction in many cardiac pathophysiologic conditions. This review discusses the cellular effectors and molecular pathways implicated in the pathogenesis of cardiac fibrosis. Although activated myofibroblasts are the main effector cells in the fibrotic heart, monocytes/macrophages, lymphocytes, mast cells, vascular cells and cardiomyocytes may also contribute to the fibrotic response by secreting key fibrogenic mediators. Inflammatory cytokines and chemokines, reactive oxygen species, mast cell-derived proteases, endothelin-1, the renin/angiotensin/aldosterone system, matricellular proteins, and growth factors (such as TGF-β and PDGF) are some of the best-studied mediators implicated in cardiac fibrosis. Both experimental and clinical evidence suggests that cardiac fibrotic alterations may be reversible. Understanding the mechanisms responsible for initiation, progression, and resolution of cardiac fibrosis is crucial to design anti-fibrotic treatment strategies for patients with heart disease.
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              MAP kinases in the immune response.

              MAP kinases are among the most ancient signal transduction pathways and are widely used throughout evolution in many physiological processes. In mammalian species, MAP kinases are involved in all aspects of immune responses, from the initiation phase of innate immunity, to activation of adaptive immunity, and to cell death when immune function is complete. In this review, we summarize recent progress in understanding the function and regulation of MAP kinase pathways in these phases of immune responses.
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                Author and article information

                Contributors
                liuzh@jlu.edu.cn
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                26 November 2020
                26 November 2020
                2020
                : 10
                : 20623
                Affiliations
                [1 ]GRID grid.64924.3d, ISNI 0000 0004 1760 5735, Department of Immunology, College of Basic Medical Sciences, , Jilin University, ; 126 Xinmin Street, Changchun, 130021 Jilin China
                [2 ]GRID grid.64924.3d, ISNI 0000 0004 1760 5735, Department of General Dentistry, School and Hospital of Stomatology, , Jilin University, ; Changchun, 130021 Jilin China
                [3 ]GRID grid.64924.3d, ISNI 0000 0004 1760 5735, Department of Genetics, College of Basic Medical Sciences, , Jilin University, ; Changchun, 130021 Jilin China
                [4 ]GRID grid.443314.5, ISNI 0000 0001 0225 0773, Department of Scientific Research, , Jilin Jianzhu University, ; Changchun, 130118 Jilin China
                Article
                77783
                10.1038/s41598-020-77783-8
                7693280
                33244088
                fb1c0dad-b79c-4d6c-be22-13dd4baf4914
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 15 April 2020
                : 17 November 2020
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100009991, Department of Finance of Jilin Province;
                Award ID: JCSZ2019378-29
                Award Recipient :
                Funded by: Science Foundation of Jilin Province
                Award ID: 2016Q039
                Award ID: 20180414040GH
                Award ID: 20200201142JC
                Award Recipient :
                Funded by: National Natural Science Foundation of China
                Award ID: 31871510
                Award Recipient :
                Categories
                Article
                Custom metadata
                © The Author(s) 2020

                Uncategorized
                cell migration,cell signalling,cytokines
                Uncategorized
                cell migration, cell signalling, cytokines

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