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      Evolving Roles of Muscle-Resident Fibro-Adipogenic Progenitors in Health, Regeneration, Neuromuscular Disorders, and Aging

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          Abstract

          Normal skeletal muscle functions are affected following trauma, chronic diseases, inherited neuromuscular disorders, aging, and cachexia, hampering the daily activities and quality of life of the affected patients. The maladaptive accumulation of fibrous intramuscular connective tissue and fat are hallmarks of multiple pathologies where chronic damage and inflammation are not resolved, leading to progressive muscle replacement and tissue degeneration. Muscle-resident fibro-adipogenic progenitors are adaptable stromal cells with multilineage potential. They are required for muscle homeostasis, neuromuscular integrity, and tissue regeneration. Fibro-adipogenic progenitors actively regulate and shape the extracellular matrix and exert immunomodulatory functions via cross-talk with multiple other residents and non-resident muscle cells. Remarkably, cumulative evidence shows that a significant proportion of activated fibroblasts, adipocytes, and bone-cartilage cells, found after muscle trauma and disease, descend from these enigmatic interstitial progenitors. Despite the profound impact of muscle disease on human health, the fibrous, fatty, and ectopic bone tissues’ origins are poorly understood. Here, we review the current knowledge of fibro-adipogenic progenitor function on muscle homeostatic integrity, regeneration, repair, and aging. We also discuss how scar-forming pathologies and disorders lead to dysregulations in their behavior and plasticity and how these stromal cells can control the onset and severity of muscle loss in disease. We finally explore the rationale of improving muscle regeneration by understanding and modulating fibro-adipogenic progenitors’ fate and behavior.

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          Most cited references238

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          The blockade of immune checkpoints in cancer immunotherapy.

          Among the most promising approaches to activating therapeutic antitumour immunity is the blockade of immune checkpoints. Immune checkpoints refer to a plethora of inhibitory pathways hardwired into the immune system that are crucial for maintaining self-tolerance and modulating the duration and amplitude of physiological immune responses in peripheral tissues in order to minimize collateral tissue damage. It is now clear that tumours co-opt certain immune-checkpoint pathways as a major mechanism of immune resistance, particularly against T cells that are specific for tumour antigens. Because many of the immune checkpoints are initiated by ligand-receptor interactions, they can be readily blocked by antibodies or modulated by recombinant forms of ligands or receptors. Cytotoxic T-lymphocyte-associated antigen 4 (CTLA4) antibodies were the first of this class of immunotherapeutics to achieve US Food and Drug Administration (FDA) approval. Preliminary clinical findings with blockers of additional immune-checkpoint proteins, such as programmed cell death protein 1 (PD1), indicate broad and diverse opportunities to enhance antitumour immunity with the potential to produce durable clinical responses.
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            Macrophage activation and polarization: nomenclature and experimental guidelines.

            Description of macrophage activation is currently contentious and confusing. Like the biblical Tower of Babel, macrophage activation encompasses a panoply of descriptors used in different ways. The lack of consensus on how to define macrophage activation in experiments in vitro and in vivo impedes progress in multiple ways, including the fact that many researchers still consider there to be only two types of activated macrophages, often termed M1 and M2. Here, we describe a set of standards encompassing three principles-the source of macrophages, definition of the activators, and a consensus collection of markers to describe macrophage activation-with the goal of unifying experimental standards for diverse experimental scenarios. Collectively, we propose a common framework for macrophage-activation nomenclature. Copyright © 2014 Elsevier Inc. All rights reserved.
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              Mechanisms of fibrosis: therapeutic translation for fibrotic disease.

              Fibrosis is a pathological feature of most chronic inflammatory diseases. Fibrosis, or scarring, is defined by the accumulation of excess extracellular matrix components. If highly progressive, the fibrotic process eventually leads to organ malfunction and death. Fibrosis affects nearly every tissue in the body. Here we discuss how key components of the innate and adaptive immune response contribute to the pathogenesis of fibrosis. We also describe how cell-intrinsic changes in important structural cells can perpetuate the fibrotic response by regulating the differentiation, recruitment, proliferation and activation of extracellular matrix-producing myofibroblasts. Finally, we highlight some of the key mechanisms and pathways of fibrosis that are being targeted as potential therapies for a variety of important human diseases.
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                Author and article information

                Contributors
                Journal
                Front Physiol
                Front Physiol
                Front. Physiol.
                Frontiers in Physiology
                Frontiers Media S.A.
                1664-042X
                20 April 2021
                2021
                : 12
                : 673404
                Affiliations
                [1] 1Biomedical Research Centre, Department of Medical Genetics, School of Biomedical Engineering, The University of British Columbia , Vancouver, BC, Canada
                [2] 2Departamento de Biología Celular y Molecular, Center for Aging and Regeneration (CARE-ChileUC), Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile , Santiago, Chile
                [3] 3St. Vincent’s Clinical School, Faculty of Medicine , UNSW Sydney, Kensington, NSW, Australia
                [4] 4Developmental and Stem Cell Biology Division, Victor Chang Cardiac Research Institute , Darlinghurst, NSW, Australia
                Author notes

                Edited by: Elvira Forte, The Jackson Laboratory, United States

                Reviewed by: Luca Madaro, Sapienza University of Rome, Italy; Lorenzo Giordani, Sorbonne Université, France

                *Correspondence: Marine Theret, mtheret@ 123456brc.ubc.ca

                This article was submitted to Integrative Physiology, a section of the journal Frontiers in Physiology

                Article
                10.3389/fphys.2021.673404
                8093402
                33959042
                9b899959-e3a5-4413-b596-5c87cf34c4c4
                Copyright © 2021 Theret, Rossi and Contreras.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 27 February 2021
                : 19 March 2021
                Page count
                Figures: 5, Tables: 0, Equations: 0, References: 238, Pages: 23, Words: 0
                Funding
                Funded by: Michael Smith Foundation for Health Research 10.13039/501100000245
                Award ID: 18351
                Funded by: Fondation pour la Recherche Médicale 10.13039/501100002915
                Award ID: 40248
                Funded by: European Molecular Biology Organization 10.13039/100004410
                Award ID: ALTF 115-2016
                Funded by: Canadian Institutes of Health Research 10.13039/501100000024
                Award ID: CIHR-FDN-159908
                Funded by: Centro de Envejecimiento y Regeneración, Pontificia Universidad Católica de Chile 10.13039/501100016011
                Award ID: CONICYT-AFB 170005
                Funded by: Comisión Nacional de Investigación Científica y Tecnológica 10.13039/501100002848
                Award ID: Beca Doctorado Nacional 2014 folio 21140378
                Categories
                Physiology
                Review

                Anatomy & Physiology
                skeletal muscle fibrosis,muscle faps,muscle regeneration,aging,muscle stem cells (muscs),macrophages,extracellular matrix (ecm),duchenne muscular dystrophy (dmd)

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