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      Inflammatory macrophages facilitate mechanical stress-induced osteogenesis

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          Abstract

          Mechanical stress has been recognized as a key inducer of bone regeneration in bone damage, which is experimentally mimicked by distraction osteogenesis (DO), a bone-regenerative process induced by post-osteotomy distraction of the surrounding vascularized bone segments, and realized by new bone formation within the distraction gap. The mechanisms that underlie the DO-induced bone regeneration remain poorly understood and a role of macrophages in the process has been inadequately studied. Here, in a mouse model of DO, we showed significant increase in macrophages in the regeneration area. Moreover, in a loss-of-function approach by depleting inflammatory macrophages, the bone regeneration was compromised by assessment of histology and molecular biology. Thus, our study demonstrates the necessary participation of inflammatory macrophages in the process of DO-induced bone regeneration, and suggests that targeting inflammatory macrophages may help to improve clinical bone repair.

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          Most cited references18

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          M1 and M2 Macrophages: Oracles of Health and Disease

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            A Subset of Chondrogenic Cells Provides Early Mesenchymal Progenitors in Growing Bones

            The hallmark of endochondral bone development is the presence of cartilaginous templates, in which osteoblasts and stromal cells are generated to form mineralized matrix and support bone marrow hematopoiesis. However, the ultimate source of these mesenchymal cells and the relationship between bone progenitors in fetal life and those in later life are unknown. Fate-mapping studies revealed that cells expressing cre-recombinases driven by the collagen II (Col2) promoter/enhancer and their descendants contributed to, in addition to chondrocytes, early perichondrial precursors prior to Runx2 expression and, subsequently, to a majority of osteoblasts, Cxcl12 (chemokine (C-X-C motif) ligand 12)-abundant stromal cells and bone marrow stromal/mesenchymal progenitor cells in postnatal life. Lineage-tracing experiments using a tamoxifen-inducible creER system further revealed that early postnatal cells marked by Col2-creER, as well as Sox9-creER and aggrecan (Acan)-creER, progressively contributed to multiple mesenchymal lineages and continued to provide descendants for over a year. These cells are distinct from adult mesenchymal progenitors and thus provide opportunities for regulating the explosive growth that occurs uniquely in growing mammals.
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              Molecular mechanisms controlling bone formation during fracture healing and distraction osteogenesis.

              Fracture healing and distraction osteogenesis have important applications in orthopedic, maxillofacial, and periodontal treatment. In this review, the cellular and molecular mechanisms that regulate fracture repair are contrasted with bone regeneration that occurs during distraction osteogenesis. While both processes have many common features, unique differences are observed in the temporal appearance and expression of specific molecular factors that regulate each. The relative importance of inflammatory cytokines in normal and diabetic healing, the transforming growth factor beta superfamily of bone morphogenetic mediators, and the process of angiogenesis are discussed as they relate to bone repair. A complete summary of biological activities and functions of various bioactive factors may be found at COPE (Cytokines & Cells Online Pathfinder Encyclopedia), http://www.copewithcytokines.de/cope.cgi.
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                Author and article information

                Journal
                Aging (Albany NY)
                Aging (Albany NY)
                Aging
                Aging (Albany NY)
                Impact Journals
                1945-4589
                29 February 2020
                25 February 2020
                : 12
                : 4
                : 3617-3625
                Affiliations
                [1 ]Department of Orthopedic Surgery, Changzheng Hospital, Second Military Medical University, Shanghai 200001, China
                [2 ]Department of Orthopedic Surgery, No. 906 Hospital of the People’s Liberation Army, Ningbo 330212, China
                [3 ]Department of Spine Surgery, LinZhou Hospital of Traditional Chinese Medicine, Linzhou 456550, China
                Author notes
                [*]

                Equal contribution

                Correspondence to: Jingchuan Sun; email: sjc8817@sina.com
                Correspondence to: Aimin Chen; email: chenaimin@163.com
                Article
                102833 102833
                10.18632/aging.102833
                7066933
                32096768
                41d862e0-9933-41e5-bd58-f9981438a54e
                Copyright © 2020 Zhang et al.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 11 December 2019
                : 27 January 2020
                Categories
                Research Paper

                Cell biology
                macrophages,mechanical stress,distraction osteogenesis (do),saporin-cd11b
                Cell biology
                macrophages, mechanical stress, distraction osteogenesis (do), saporin-cd11b

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