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      Flavonoid Glycosides from Ulmus macrocarpa Inhibit Osteoclast Differentiation via the Downregulation of NFATc1

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          Abstract

          The aim of this study was to isolate and identify chemical components with osteoclast differentiation inhibitory activity from Ulmus macrocarpa Hance bark. Spectroscopic analyses, including nuclear magnetic resonance (NMR) and electronic circular dichroism (ECD), resulted in the unequivocal elucidation of active compounds such as (2 S)-naringenin-6- C-β- d-glucopyranoside ( 1), (2 R)-naringenin-6- C-β- d-glucopyranoside ( 2), (2 R,3 S)-catechin-7- O-β- d-xylopyranoside ( 3), (2 R,3 S)-catechin-7- O-β- d-apiofuranoside ( 6), (2 R,3 R)-taxifolin-6- C-β- d-glucopyranoside ( 7), and (2 S,3 S)-taxifolin-6- C-β- d-glucopyranoside ( 8). Mechanistically, the compounds may exhibit osteoclast differentiation inhibitory activity via the downregulation of NFATc1, a master regulator involved in osteoclast formation. This is the first report of their inhibitory activities on the receptor activator of nuclear factor κB ligand (RANKL)-induced osteoclast differentiation in murine bone marrow-derived macrophages. These findings provide further scientific evidence for the rational application of the genus Ulmus for the amelioration or treatment of osteopenic diseases.

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          Most cited references47

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          Osteoclast differentiation and activation.

          Osteoclasts are specialized cells derived from the monocyte/macrophage haematopoietic lineage that develop and adhere to bone matrix, then secrete acid and lytic enzymes that degrade it in a specialized, extracellular compartment. Discovery of the RANK signalling pathway in the osteoclast has provided insight into the mechanisms of osteoclastogenesis and activation of bone resorption, and how hormonal signals impact bone structure and mass. Further study of this pathway is providing the molecular basis for developing therapeutics to treat osteoporosis and other diseases of bone loss.
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            Osteoimmunology: shared mechanisms and crosstalk between the immune and bone systems.

            Osteoimmunology is an interdisciplinary research field focused on the molecular understanding of the interplay between the immune and skeletal systems. Although osteoimmunology started with the study of the immune regulation of osteoclasts, its scope has been extended to encompass a wide range of molecular and cellular interactions, including those between osteoblasts and osteoclasts, lymphocytes and osteoclasts, and osteoblasts and haematopoietic cells. Therefore, the two systems should be understood to be integrated and operating in the context of the 'osteoimmune' system, a heuristic concept that provides not only a framework for obtaining new insights by basic research, but also a scientific basis for the discovery of novel treatments for diseases related to both systems.
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              The molecular understanding of osteoclast differentiation.

              Osteoclasts are multinucleated cells of monocyte/macrophage origin that degrade bone matrix. The differentiation of osteoclasts is dependent on a tumor necrosis factor (TNF) family cytokine, receptor activator of nuclear factor (NF)-kappaB ligand (RANKL), as well as macrophage colony-stimulating factor (M-CSF). Congenital lack of osteoclasts causes osteopetrosis, investigation of which has provided insights into the essential molecules for osteoclastogenesis, including TNF receptor-associated factor (TRAF) 6, NF-kappaB and c-Fos. In addition, genome-wide screening techniques have shed light on an additional set of gene products such as nuclear factor of activated T cells (NFAT) c1. Here we summarize the efforts to understand the sequential molecular events induced by RANKL during osteoclast differentiation. RANKL binds to its receptor RANK, which recruits adaptor molecules such as TRAF6. TRAF6 activates NF-kappaB, which is important for the initial induction of NFATc1. NFATc1 is activated by calcium signaling and binds to its own promoter, thus switching on an autoregulatory loop. An activator protein (AP)-1 complex containing c-Fos is required for the autoamplification of NFATc1, enabling the robust induction of NFATc1. Finally, NFATc1 cooperates with other transcriptional partners to activate osteoclast-specific genes. NFATc1 autoregulation is controlled by an epigenetic mechanism, which has profound implications for an understanding of the general mechanism of irreversible cell fate determination. From the clinical point of view, RANKL signaling pathway has promise as a strategy for suppressing the excessive osteoclast formation characteristic of a variety of bone diseases.
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                Author and article information

                Journal
                ACS Omega
                ACS Omega
                ao
                acsodf
                ACS Omega
                American Chemical Society
                2470-1343
                31 January 2022
                15 February 2022
                : 7
                : 6
                : 4840-4849
                Affiliations
                []Laboratory of Marine Drugs, School of Earth and Environmental Sciences, Seoul National University , Seoul 08826, Korea
                []Research Institute of Oceanography, Seoul National University , NS-80, Seoul 08826, Korea
                [§ ]Department of Agricultural Biotechnology and Research Institute of Agriculture and Life Sciences, Seoul National University , Seoul 08826, Korea
                []Department of Pharmacy, Sunchon National University , 315 Maegok-dong, Suncheon, Jeollanam-do 57922, Korea
                []Interdisciplinary Graduate Program in Genetic Engineering, Seoul National University , NS-80, Seoul 08826, Korea
                [# ]Bio-MAX Institute, Seoul National University , Seoul 08826, Korea
                []Advanced Institutes of Convergence Technology, Seoul National University , Suwon 16229, Korea
                Author notes
                Author information
                https://orcid.org/0000-0001-5555-2898
                Article
                10.1021/acsomega.1c05305
                8851653
                35187304
                dd614b4d-d890-4821-a65b-613e85dc0709
                © 2022 The Authors. Published by American Chemical Society

                Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works ( https://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 24 September 2021
                : 21 January 2022
                Funding
                Funded by: Ministry of Science, ICT and Future Planning, doi 10.13039/501100003621;
                Award ID: 2019R1A2C2005492
                Funded by: Pyeongchang Revitalizing Program, doi NA;
                Award ID: NA
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                Custom metadata
                ao1c05305
                ao1c05305

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