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      Discovery and optimized extraction of the anti-osteoclastic agent epicatechin-7-O-β-D-apiofuranoside from Ulmus macrocarpa Hance bark

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          Abstract

          Ulmus macrocarpa Hance bark ( UmHb) has been used as a traditional herbal medicine in East Asia for bone concern diseases for a long time. To find a suitable solvent, we, in this study, compared the efficacy of UmHb water extract and ethanol extract which can inhibit osteoclast differentiation. Compared with two ethanol extracts (70% and 100% respectively), hydrothermal extracts of UmHb more effectively inhibited receptor activators of nuclear factor κB ligand-induced osteoclast differentiation in murine bone marrow-derived macrophages. We identified for the first time that (2R,3R)-epicatechin-7-O-β-D-apiofuranoside (E7A) is a specific active compound in UmHb hydrothermal extracts through using LC/MS, HPLC, and NMR techniques. In addition, we confirmed through TRAP assay, pit assay, and PCR assay that E7A is a key compound in inhibiting osteoclast differentiation. The optimized condition to obtain E7A-rich UmHb extract was 100 mL/g, 90 °C, pH 5, and 97 min. At this condition, the content of E7A was 26.05 ± 0.96 mg/g extract. Based on TRAP assay, pit assay, PCR, and western blot, the optimized extract of E7A-rich UmHb demonstrated a greater inhibition of osteoclast differentiation compared to unoptimized. These results suggest that E7A would be a good candidate for the prevention and treatment of osteoporosis-related diseases.

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          Most cited references38

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          Control of osteoblast function and regulation of bone mass.

          The skeleton is an efficient 'servo' (feedback-controlled/steady-state) system that continuously integrates signals and responses which sustain its functions of delivering calcium while maintaining strength. In many individuals, bone mass homeostasis starts failing in midlife, leading to bone loss, osteoporosis and debilitating fractures. Recent advances, spearheaded by genetic information, offer the opportunity to stop or reverse this downhill course.
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            Induction and activation of the transcription factor NFATc1 (NFAT2) integrate RANKL signaling in terminal differentiation of osteoclasts.

            Signaling by RANKL is essential for terminal differentiation of monocytes/macrophages into osteoclasts. The TRAF6 and c-Fos signaling pathways both play important roles downstream of RANKL. We show here that RANKL selectively induces NFATc1 expression via these two pathways. RANKL also evokes Ca(2+) oscillations that lead to calcineurin-mediated activation of NFATc1, and therefore triggers a sustained NFATc1-dependent transcriptional program during osteoclast differentiation. We also show that NFATc1-deficient embryonic stem cells fail to differentiate into osteoclasts in response to RANKL stimulation, and that ectopic expression of NFATc1 causes precursor cells to undergo efficient differentiation without RANKL signaling. Thus, NFATc1 may represent a master switch for regulating terminal differentiation of osteoclasts, functioning downstream of RANKL.
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              Osteoblast-Osteoclast Communication and Bone Homeostasis

              Bone remodeling is tightly regulated by a cross-talk between bone-forming osteoblasts and bone-resorbing osteoclasts. Osteoblasts and osteoclasts communicate with each other to regulate cellular behavior, survival and differentiation through direct cell-to-cell contact or through secretory proteins. A direct interaction between osteoblasts and osteoclasts allows bidirectional transduction of activation signals through EFNB2-EPHB4, FASL-FAS or SEMA3A-NRP1, regulating differentiation and survival of osteoblasts or osteoclasts. Alternatively, osteoblasts produce a range of different secretory molecules, including M-CSF, RANKL/OPG, WNT5A, and WNT16, that promote or suppress osteoclast differentiation and development. Osteoclasts also influence osteoblast formation and differentiation through secretion of soluble factors, including S1P, SEMA4D, CTHRC1 and C3. Here we review the current knowledge regarding membrane bound- and soluble factors governing cross-talk between osteoblasts and osteoclasts.
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                Author and article information

                Contributors
                kiwon@snu.ac.kr
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                9 July 2023
                9 July 2023
                2023
                : 13
                : 11102
                Affiliations
                [1 ]GRID grid.31501.36, ISNI 0000 0004 0470 5905, Department of Agricultural Biotechnology and Research Institute of Agriculture and Life Sciences, , Seoul National University, ; Seoul, 08826 Korea
                [2 ]GRID grid.31501.36, ISNI 0000 0004 0470 5905, Bio-MAX Institute, , Seoul National University, ; Seoul, 08826 Korea
                [3 ]GRID grid.412871.9, ISNI 0000 0000 8543 5345, Department of Pharmacy, , Sunchon National University, ; 315 Maegok-dong, Suncheon, Jeollanam-do 57922 Korea
                [4 ]GRID grid.31501.36, ISNI 0000 0004 0470 5905, Laboratory of Marine Drugs, School of Earth and Environmental Sciences, , Seoul National University, ; NS-80, Seoul, 08826 Korea
                [5 ]GRID grid.31501.36, ISNI 0000 0004 0470 5905, Research Institute of Oceanography, , Seoul National University, ; NS-80, Seoul, 08826 Korea
                [6 ]GRID grid.31501.36, ISNI 0000 0004 0470 5905, Interdisciplinary Graduate Program in Genetic Engineering, , Seoul National University, ; NS-80, Seoul, 08826 Korea
                [7 ]GRID grid.31501.36, ISNI 0000 0004 0470 5905, Advanced Institutes of Convergence Technology, , Seoul National University, ; Suwon, 16229 Korea
                [8 ]GRID grid.31501.36, ISNI 0000 0004 0470 5905, Institutes of Green Bio Science and Technology, , Seoul National University, ; Pyeongchang, 25354 Korea
                [9 ]GRID grid.31501.36, ISNI 0000 0004 0470 5905, Department of Agricultural Biotechnology and Center for Food and Bio convergence, , Seoul National University, ; Seoul, 08826 Korea
                Article
                38208
                10.1038/s41598-023-38208-4
                10330169
                37423923
                a7555fc5-8b5d-43a3-94d9-c084b36c88d1
                © The Author(s) 2023

                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
                : 20 October 2022
                : 5 July 2023
                Categories
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                © Springer Nature Limited 2023

                Uncategorized
                chemical biology,drug discovery
                Uncategorized
                chemical biology, drug discovery

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