Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Advertisement

Scientific Reports
  • View all journals
  • Search
  • My Account Login
  • Content Explore content
  • About the journal
  • Publish with us
  • Sign up for alerts
  • RSS feed
  1. nature
  2. scientific reports
  3. articles
  4. article
Punicalagin with anti-inflammatory activities affects Brd-4 mediated chromatin remodeling for attenuating inflammatory osteolysis
Download PDF
Download PDF
  • Article
  • Open access
  • Published: 10 March 2026

Punicalagin with anti-inflammatory activities affects Brd-4 mediated chromatin remodeling for attenuating inflammatory osteolysis

  • Huiping Li1 na1,
  • Qilin Li1 na1,
  • Tianhao Wan1,
  • Yexin Wang1 &
  • …
  • Shanyong Zhang1 

Scientific Reports , Article number:  (2026) Cite this article

  • 710 Accesses

  • Metrics details

We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Biochemistry
  • Cell biology
  • Diseases
  • Drug discovery
  • Immunology
  • Molecular biology

Abstract

Inflammatory osteolysis is primarily characterized by an extensive macrophage-mediated inflammatory response coupled with osteoclast (OC) formation, triggered by bacterial byproducts and/or environmental stressors. And Osteoarthritis (OA) is one of the most common degenerative diseases in clinical medicine. Currently, anti-inflammatory drugs and intra-articular drug injection are mainly used, but the treatments only relieve symptoms. Punicalagin (PUN), a hydrolyzable tannin derived from pomegranate extract, the suppression of pro-inflammatory cytokine production in macrophages. The therapeutic potential of PUN in alleviating inflammatory osteolysis remains inadequately elucidated. PUN demonstrated favourable biocompatibility and therapeutic potential in vitro, including potent anti-osteoclastic activity, ROS scavenging capacity, and epigenetic regulatory functions. PUN was found to inhibit bromodomain-containing protein 4 (Brd4)-mediated chromatin space remodeling, consequently upregulating the production of endogenous anti-inflammatory factors and antioxidant factors. This study reveals a new therapeutic mechanism that PUN exerts anti-inflammatory effects and regulates epigenetic regulation by influencing Brd4-mediated chromatin remodeling. These findings showed the therapeutic potential of PUN for inflammatory diseases, especially inflammatory osteolysis. Notably, our work identifies a new strategy that synergistically combines osteoclast inhibition with epigenetic regulation, providing a promising direction for the therapies for bone-related inflammatory diseases.

Similar content being viewed by others

Osteoarthritis: molecular pathogenesis and potential therapeutic options

Article Open access 04 March 2026

Specific inflammatory osteoclast precursors induced during chronic inflammation give rise to highly active osteoclasts associated with inflammatory bone loss

Article Open access 08 April 2022

Inhibition of complement C3 prevents osteoarthritis progression in guinea pigs by blocking STAT1 activation

Article Open access 27 March 2024

Data availability

The data that support the findings of this study are available from the corresponding author upon reasonable request. The datasets generated and/or analyzed during the current study are available in https://www.ncbi.nlm.nih.gov/sra/PRJNA1328197, BioProject ID: PRJNA1328197.

References

  1. Wu, H. et al. Artemether attenuates LPS-induced inflammatory bone loss by inhibiting osteoclastogenesis and bone resorption via suppression of MAPK signaling pathway. Cell Death Dis. 9(5), 498. https://doi.org/10.1038/s41419-018-0540-y (2018).

    Google Scholar 

  2. Kassem, A. et al. Porphyromonas gingivalis stimulates bone resorption by enhancing RANKL (Receptor Activator of NF-κB Ligand) through activation of toll-like receptor 2 in osteoblasts. J. Biol. Chem. 290(33), 20147–20158. https://doi.org/10.1074/jbc.M115.655787 (2015) (In Eng).

    Google Scholar 

  3. Matheus, H. R., Ozdemir, S. D. & Guastaldi, F. P. S. Stem cell-based therapies for temporomandibular joint osteoarthritis and regeneration of cartilage/osteochondral defects: A systematic review of preclinical experiments. Osteoarthr. Cartil. 30(9), 1174–1185. https://doi.org/10.1016/j.joca.2022.05.006 (2022).

    Google Scholar 

  4. Wang, D. et al. Recent advances in animal models, diagnosis, and treatment of temporomandibular joint osteoarthritis. Tissue Eng. Part B Rev. 29(1), 62–77. https://doi.org/10.1089/ten.TEB.2022.0065 (2023).

    Google Scholar 

  5. Cardoneanu, A. et al. Temporomandibular joint osteoarthritis: Pathogenic mechanisms involving the cartilage and subchondral bone, and potential therapeutic strategies for joint regeneration. Int. J. Mol. Sci. https://doi.org/10.3390/ijms24010171 (2022).

    Google Scholar 

  6. Li, B., Guan, G., Mei, L., Jiao, K. & Li, H. Pathological mechanism of chondrocytes and the surrounding environment during osteoarthritis of temporomandibular joint. J. Cell. Mol. Med. 25(11), 4902–4911. https://doi.org/10.1111/jcmm.16514 (2021).

    Google Scholar 

  7. Mbalaviele, G., Novack, D. V., Schett, G. & Teitelbaum, S. L. Inflammatory osteolysis: A conspiracy against bone. J. Clin. Invest. 127(6), 2030–2039. https://doi.org/10.1172/JCI93356 (2017).

    Google Scholar 

  8. Kandahari, A. M. et al. A review of UHMWPE wear-induced osteolysis: The role for early detection of the immune response. Bone Res. 4, 16014. https://doi.org/10.1038/boneres.2016.14 (2016).

    Google Scholar 

  9. Hodges, N. A., Sussman, E. M. & Stegemann, J. P. Aseptic and septic prosthetic joint loosening: Impact of biomaterial wear on immune cell function, inflammation, and infection. Biomaterials 278, 121127. https://doi.org/10.1016/j.biomaterials.2021.121127 (2021).

    Google Scholar 

  10. Gruber, R. Osteoimmunology: Inflammatory osteolysis and regeneration of the alveolar bone. J. Clin. Periodontol. 46(21), 52–69. https://doi.org/10.1111/jcpe.13056 (2019).

    Google Scholar 

  11. Kwak, S. C. et al. Umbelliferone prevents lipopolysaccharide-induced bone loss and suppresses RANKL-induced osteoclastogenesis by attenuating Akt-c-Fos-NFATc1 signaling. Int. J. Biol. Sci. 15(11), 2427–2437. https://doi.org/10.7150/ijbs.28609 (2019).

    Google Scholar 

  12. O’Brien, W. et al. RANK-independent osteoclast formation and bone erosion in inflammatory arthritis. Arthritis Rheumatol. 68(12), 2889–2900. https://doi.org/10.1002/art.39837 (2016).

    Google Scholar 

  13. Wei, S., Kitaura, H., Zhou, P., Ross, F. P. & Teitelbaum, S. L. IL-1 mediates TNF-induced osteoclastogenesis. J. Clin. Invest. 115(2), 282–290. https://doi.org/10.1172/JCI23394 (2005).

    Google Scholar 

  14. Zeng, C. et al. Relative efficacy and safety of topical non-steroidal anti-inflammatory drugs for osteoarthritis: A systematic review and network meta-analysis of randomised controlled trials and observational studies. Br. J. Sports Med. 52(10), 642–650. https://doi.org/10.1136/bjsports-2017-098043 (2018).

    Google Scholar 

  15. Cooper, C. & Jordan, K. M. Topical NSAIDs in osteoarthritis. BMJ 329(7461), 304–305. https://doi.org/10.1136/bmj.329.7461.304 (2004).

    Google Scholar 

  16. Kloppenburg, M. Hand osteoarthritis-nonpharmacological and pharmacological treatments. Nat. Rev. Rheumatol. 10(4), 242–251. https://doi.org/10.1038/nrrheum.2013.214 (2014).

    Google Scholar 

  17. Jones, I. A., Togashi, R., Wilson, M. L., Heckmann, N. & Vangsness, C. T. Jr. Intra-articular treatment options for knee osteoarthritis. Nat. Rev. Rheumatol. 15(2), 77–90. https://doi.org/10.1038/s41584-018-0123-4 (2019).

    Google Scholar 

  18. Ishii, K. A. et al. Coordination of PGC-1beta and iron uptake in mitochondrial biogenesis and osteoclast activation. Nat. Med. 15(3), 259–266. https://doi.org/10.1038/nm.1910 (2009).

    Google Scholar 

  19. Wu, Z., Qu, J., Zhang, W. & Liu, G. H. Stress, epigenetics, and aging: Unraveling the intricate crosstalk. Mol. Cell 84(1), 34–54. https://doi.org/10.1016/j.molcel.2023.10.006 (2024).

    Google Scholar 

  20. Rice, S. J., Beier, F., Young, D. A. & Loughlin, J. Interplay between genetics and epigenetics in osteoarthritis. Nat. Rev. Rheumatol. 16(5), 268–281. https://doi.org/10.1038/s41584-020-0407-3 (2020).

    Google Scholar 

  21. Nunez-Carro, C., Blanco-Blanco, M., Villagran-Andrade, K. M., Blanco, F. J. & de Andres, M. C. Epigenetics as a therapeutic target in osteoarthritis. Pharmaceuticals (Basel) https://doi.org/10.3390/ph16020156 (2023).

    Google Scholar 

  22. Min, J., Feng, Q., Li, Z., Zhang, Y. & Xu, R. M. Structure of the catalytic domain of human DOT1L, a non-SET domain nucleosomal histone methyltransferase. Cell 112(5), 711–723. https://doi.org/10.1016/s0092-8674(03)00114-4 (2003).

    Google Scholar 

  23. Assi, R. et al. Inhibition of KDM7A/B histone demethylases restores H3K79 methylation and protects against osteoarthritis. Ann. Rheum. Dis. 82(7), 963–973. https://doi.org/10.1136/ard-2022-223789 (2023).

    Google Scholar 

  24. Loughlin, J. & Reynard, L. N. Osteoarthritis: Epigenetics of articular cartilage in knee and hip OA. Nat. Rev. Rheumatol. 11(1), 6–7. https://doi.org/10.1038/nrrheum.2014.189 (2015).

    Google Scholar 

  25. Lauterbach, M. A. et al. Toll-like receptor signaling rewires macrophage metabolism and promotes histone acetylation via ATP-citrate lyase. Immunity 51(6), 997-1011 e7. https://doi.org/10.1016/j.immuni.2019.11.009 (2019).

    Google Scholar 

  26. Ji, Q. et al. Hematopoietic PBX-interacting protein mediates cartilage degeneration during the pathogenesis of osteoarthritis. Nat. Commun. 10(1), 313. https://doi.org/10.1038/s41467-018-08277-5 (2019).

    Google Scholar 

  27. Haynes, S. R. et al. The bromodomain: A conserved sequence found in human, Drosophila and yeast proteins. Nucleic Acids Res. 20(10), 2603. https://doi.org/10.1093/nar/20.10.2603 (1992).

    Google Scholar 

  28. Jang, M. K. et al. The bromodomain protein Brd4 is a positive regulatory component of P-TEFb and stimulates RNA polymerase II-dependent transcription. Mol. Cell 19(4), 523–534. https://doi.org/10.1016/j.molcel.2005.06.027 (2005).

    Google Scholar 

  29. Yang, Z. et al. Recruitment of P-TEFb for stimulation of transcriptional elongation by the bromodomain protein Brd4. Mol. Cell 19(4), 535–545. https://doi.org/10.1016/j.molcel.2005.06.029 (2005).

    Google Scholar 

  30. Itzen, F., Greifenberg, A. K., Bosken, C. A. & Geyer, M. Brd4 activates P-TEFb for RNA polymerase II CTD phosphorylation. Nucleic Acids Res. 42(12), 7577–7590. https://doi.org/10.1093/nar/gku449 (2014).

    Google Scholar 

  31. Nicodeme, E. et al. Suppression of inflammation by a synthetic histone mimic. Nature 468(7327), 1119–1123. https://doi.org/10.1038/nature09589 (2010).

    Google Scholar 

  32. Filippakopoulos, P. et al. Selective inhibition of BET bromodomains. Nature 468(7327), 1067–1073. https://doi.org/10.1038/nature09504 (2010).

    Google Scholar 

  33. Wang, Z. Q. et al. Bromodomain and extraterminal (BET) proteins: Biological functions, diseases, and targeted therapy. Signal Transduct. Target. Ther. 8(1), 420. https://doi.org/10.1038/s41392-023-01647-6 (2023).

    Google Scholar 

  34. Park-Min, K. H. et al. Inhibition of osteoclastogenesis and inflammatory bone resorption by targeting BET proteins and epigenetic regulation. Nat. Commun. 5, 5418. https://doi.org/10.1038/ncomms6418 (2014).

    Google Scholar 

  35. Tao, X., Yin, L., Xu, L. & Peng, J. Dioscin: A diverse acting natural compound with therapeutic potential in metabolic diseases, cancer, inflammation and infections. Pharmacol. Res. 137, 259–269. https://doi.org/10.1016/j.phrs.2018.09.022 (2018).

    Google Scholar 

  36. Atanasov, A. G. et al. Discovery and resupply of pharmacologically active plant-derived natural products: A review. Biotechnol. Adv. 33(8), 1582–1614. https://doi.org/10.1016/j.biotechadv.2015.08.001 (2015).

    Google Scholar 

  37. Ge, G. et al. Punicalagin ameliorates collagen-induced arthritis by downregulating M1 macrophage and pyroptosis via NF-κB signaling pathway. Sci. China Life Sci. 65(3), 588–603. https://doi.org/10.1007/s11427-020-1939-1 (2022).

    Google Scholar 

  38. Wang, W. et al. Protective effects of Punicalagin on osteoporosis by inhibiting osteoclastogenesis and inflammation via the NF-κB and MAPK pathways. Front. Pharmacol. 11, 696. https://doi.org/10.3389/fphar.2020.00696 (2020).

    Google Scholar 

  39. Olajide, O. A., Kumar, A., Velagapudi, R., Okorji, U. P. & Fiebich, B. L. Punicalagin inhibits neuroinflammation in LPS-activated rat primary microglia. Mol. Nutr. Food Res. 58(9), 1843–1851. https://doi.org/10.1002/mnfr.201400163 (2014).

    Google Scholar 

  40. Xu, X. et al. Punicalagin Inhibits Inflammation in LPS-Induced RAW264.7 Macrophages via the Suppression of TLR4-Mediated MAPKs and NF-κB Activation. Inflammation 37(3), 956–965. https://doi.org/10.1007/s10753-014-9816-2 (2014).

    Google Scholar 

  41. Glyn-Jones, S. et al. Osteoarthritis. Lancet 386(9991), 376–387. https://doi.org/10.1016/S0140-6736(14)60802-3 (2015).

    Google Scholar 

  42. Wu, Y. L. et al. Propionate and butyrate attenuate macrophage pyroptosis and osteoclastogenesis induced by CoCrMo alloy particles. Mil. Med. Res. 9(1), 46. https://doi.org/10.1186/s40779-022-00404-0 (2022).

    Google Scholar 

  43. Yoshimoto, T. et al. Osteocytes directly regulate osteolysis via MYD88 signaling in bacterial bone infection. Nat. Commun. 13(1), 6648. https://doi.org/10.1038/s41467-022-34352-z (2022).

    Google Scholar 

  44. Li, Y. et al. Urolithin B suppressed osteoclast activation and reduced bone loss of osteoporosis via inhibiting ERK/NF-kappaB pathway. Cell Prolif 55(10), e13291. https://doi.org/10.1111/cpr.13291 (2022).

    Google Scholar 

  45. Devaiah, B. N. et al. BRD4 is a histone acetyltransferase that evicts nucleosomes from chromatin. Nat. Struct. Mol. Biol. 23(6), 540–548. https://doi.org/10.1038/nsmb.3228 (2016).

    Google Scholar 

  46. Lamoureux, F. et al. Selective inhibition of BET bromodomain epigenetic signalling interferes with the bone-associated tumour vicious cycle. Nat. Commun. 5, 3511. https://doi.org/10.1038/ncomms4511 (2014).

    Google Scholar 

  47. Cerda, B., Llorach, R., Ceron, J. J., Espin, J. C. & Tomas-Barberan, F. A. Evaluation of the bioavailability and metabolism in the rat of punicalagin, an antioxidant polyphenol from pomegranate juice. Eur. J. Nutr. 42(1), 18–28. https://doi.org/10.1007/s00394-003-0396-4 (2003).

    Google Scholar 

  48. Wang, Q. et al. Punicalagin ameliorates wear-particle-induced inflammatory bone destruction by bi-directional regulation of osteoblastic formation and osteoclastic resorption. Biomater. Sci. 8(18), 5157–5171. https://doi.org/10.1039/d0bm00718h (2020).

    Google Scholar 

  49. Iwatake, M., Okamoto, K., Tanaka, T. & Tsukuba, T. Punicalagin attenuates osteoclast differentiation by impairing NFATc1 expression and blocking Akt- and JNK-dependent pathways. Mol. Cell. Biochem. 407(1–2), 161–172. https://doi.org/10.1007/s11010-015-2466-3 (2015).

    Google Scholar 

  50. Chen, X. et al. Ultrasmall PtAu(2) nanoclusters activate endogenous anti-inflammatory and anti-oxidative systems to prevent inflammatory osteolysis. Theranostics 13(3), 1010–1027. https://doi.org/10.7150/thno.80514 (2023).

    Google Scholar 

  51. Chen, X. et al. LY411575, a potent gamma-secretase inhibitor, suppresses osteoclastogenesis in vitro and LPS-induced calvarial osteolysis in vivo. J. Cell. Physiol. 234(11), 20944–20956. https://doi.org/10.1002/jcp.28699 (2019).

    Google Scholar 

  52. Chen, X. et al. Nirogacestat suppresses RANKL-induced osteoclast formation in vitro and attenuates LPS-induced bone resorption in vivo. Exp. Cell Res. 382(1), 111470. https://doi.org/10.1016/j.yexcr.2019.06.015 (2019).

    Google Scholar 

  53. Yao, H. et al. Sulforaphene suppresses RANKL-induced osteoclastogenesis and LPS-induced bone erosion by activating Nrf2 signaling pathway. Free Radic. Biol. Med. 207, 48–62. https://doi.org/10.1016/j.freeradbiomed.2023.07.009 (2023).

    Google Scholar 

Download references

Acknowledgements

The authors would like to thank Editage (www.editage.cn) for the professional English language editing service. There is no founding.

Author information

Author notes
  1. Huiping Li and Qilin Li are co-first authors and contributed equally to this study.

Authors and Affiliations

  1. Department of Oral Surgery, Shanghai Ninth People’s Hospital, Shanghai Jiao Tong University School of Medicine; College of Stomatology, Shanghai Jiao Tong University; National Center for Stomatology; National Clinical Research Center for Oral Diseases; Shanghai Key Laboratory of Stomatology, Shanghai, 200011, China

    Huiping Li, Qilin Li, Tianhao Wan, Yexin Wang & Shanyong Zhang

Authors
  1. Huiping Li
    View author publications

    Search author on:PubMed Google Scholar

  2. Qilin Li
    View author publications

    Search author on:PubMed Google Scholar

  3. Tianhao Wan
    View author publications

    Search author on:PubMed Google Scholar

  4. Yexin Wang
    View author publications

    Search author on:PubMed Google Scholar

  5. Shanyong Zhang
    View author publications

    Search author on:PubMed Google Scholar

Contributions

Dr. Huiping Li contributes to conceptualization, the project administration and supervision; Dr. Qilin Li and Dr. Tianhao Wan contribute to data curation and formal analysis; Dr. Yexin Wang and Prof. Shanyong Zhang contribute to investigation, original draft writing, review and editing.

Corresponding authors

Correspondence to Yexin Wang or Shanyong Zhang.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Below is the link to the electronic supplementary material.

Supplementary Material 1 (download PDF )

Rights and permissions

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/.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Li, H., Li, Q., Wan, T. et al. Punicalagin with anti-inflammatory activities affects Brd-4 mediated chromatin remodeling for attenuating inflammatory osteolysis. Sci Rep (2026). https://doi.org/10.1038/s41598-026-41262-3

Download citation

  • Received: 03 September 2025

  • Accepted: 19 February 2026

  • Published: 10 March 2026

  • DOI: https://doi.org/10.1038/s41598-026-41262-3

Share this article

Anyone you share the following link with will be able to read this content:

Sorry, a shareable link is not currently available for this article.

Provided by the Springer Nature SharedIt content-sharing initiative

Keywords

  • Punicalagin
  • Osteolysis
  • Osteoclast
  • Brd4
  • Inflammatory macrophage
Download PDF

Advertisement

Explore content

  • Research articles
  • News & Comment
  • Collections
  • Subjects
  • Follow us on Facebook
  • Follow us on X
  • Sign up for alerts
  • RSS feed

About the journal

  • About Scientific Reports
  • Contact
  • Journal policies
  • Guide to referees
  • Calls for Papers
  • Editor's Choice
  • Journal highlights
  • Open Access Fees and Funding

Publish with us

  • For authors
  • Language editing services
  • Open access funding
  • Submit manuscript

Search

Advanced search

Quick links

  • Explore articles by subject
  • Find a job
  • Guide to authors
  • Editorial policies

Scientific Reports (Sci Rep)

ISSN 2045-2322 (online)

nature.com footer links

About Nature Portfolio

  • About us
  • Press releases
  • Press office
  • Contact us

Discover content

  • Journals A-Z
  • Articles by subject
  • protocols.io
  • Nature Index

Publishing policies

  • Nature portfolio policies
  • Open access

Author & Researcher services

  • Reprints & permissions
  • Research data
  • Language editing
  • Scientific editing
  • Nature Masterclasses
  • Research Solutions

Libraries & institutions

  • Librarian service & tools
  • Librarian portal
  • Open research
  • Recommend to library

Advertising & partnerships

  • Advertising
  • Partnerships & Services
  • Media kits
  • Branded content

Professional development

  • Nature Awards
  • Nature Careers
  • Nature Conferences

Regional websites

  • Nature Africa
  • Nature China
  • Nature India
  • Nature Japan
  • Nature Middle East
  • Privacy Policy
  • Use of cookies
  • Legal notice
  • Accessibility statement
  • Terms & Conditions
  • Your US state privacy rights
Springer Nature

© 2026 Springer Nature Limited

Nature Briefing: Translational Research

Sign up for the Nature Briefing: Translational Research newsletter — top stories in biotechnology, drug discovery and pharma.

Get what matters in translational research, free to your inbox weekly. Sign up for Nature Briefing: Translational Research