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<p>Osteoarthritis (OA) is recognized as the most common chronic joint disease, characterized primarily by the degeneration of articular cartilage. Through screening a natural product library, we identified periplocin as a candidate agent capable of promoting chondrocyte anabolism. Periplocin, a cardiotonic steroid isolated from <i>Periploca forrestii</i>, has been proven to be involved in antiinflammatory responses. However, the role and mechanism of periplocin in OA have not been confirmed. This study aims to explore the biological role and potential of periplocin in chondrocyte metabolism and OA treatment. A drug library was screened to identify candidate components that promote chondrocyte anabolism. In vitro experiments showed that periplocin could promote chondrocyte anabolism, enhance chondrogenic differentiation, and inhibit inflammation-induced chondrocyte catabolism. Using a surgically induced destabilization of the medial meniscus (DMM) OA mice model, combined with histological staining, micro-computed tomography, and behavioral assessments, we confirmed that periplocin alleviated cartilage degeneration, suppressed osteophyte formation, improved motor function, and relieved OA-related pain in DMM mice. Molecular docking, Drug Affinity Responsive Target Stability (DARTS) assay, Cellular Thermal Shift Assay (CETSA), and Molecular dynamic (MD) simulation identified LRP4 as the key target of periplocin, with Asp812 serving as its critical binding site. With the help of CRISPR-Cas9 gene editing to knock out low-density lipoprotein receptor-related protein 4 (LRP4) in C28I2 and generate chondrocyte-specific <i>Lrp4</i> knockout mice, the dependence of periplocin-mediated regulation of chondrocyte function on LRP4 was verified. This study not only provides new insights into understanding the chondroprotective effect of periplocin targeting LRP4 and its underlying mechanism but also offers experimental evidence for the use of periplocin as a potential disease-modifying OA drug (DMOAD) in OA treatment.</p>

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Periplocin targets low density lipoprotein receptor-related protein 4 and protects against osteoarthritis

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2026年7月31日

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  • Jincheng Liu,
  • Qingyang Fu,
  • Chunlin Li,
  • Kun Gao,
  • Mengsi Sun,
  • Mingyu Xu,
  • Junfei Chen,
  • Xu Zhai,
  • Wencan Zhang,
  • Le Li,
  • Wanlong Xu,
  • Yang Liu,
  • Xinhui Wu,
  • Haipeng Si,
  • Kaidi Wang

摘要

Osteoarthritis (OA) is recognized as the most common chronic joint disease, characterized primarily by the degeneration of articular cartilage. Through screening a natural product library, we identified periplocin as a candidate agent capable of promoting chondrocyte anabolism. Periplocin, a cardiotonic steroid isolated from Periploca forrestii, has been proven to be involved in antiinflammatory responses. However, the role and mechanism of periplocin in OA have not been confirmed. This study aims to explore the biological role and potential of periplocin in chondrocyte metabolism and OA treatment. A drug library was screened to identify candidate components that promote chondrocyte anabolism. In vitro experiments showed that periplocin could promote chondrocyte anabolism, enhance chondrogenic differentiation, and inhibit inflammation-induced chondrocyte catabolism. Using a surgically induced destabilization of the medial meniscus (DMM) OA mice model, combined with histological staining, micro-computed tomography, and behavioral assessments, we confirmed that periplocin alleviated cartilage degeneration, suppressed osteophyte formation, improved motor function, and relieved OA-related pain in DMM mice. Molecular docking, Drug Affinity Responsive Target Stability (DARTS) assay, Cellular Thermal Shift Assay (CETSA), and Molecular dynamic (MD) simulation identified LRP4 as the key target of periplocin, with Asp812 serving as its critical binding site. With the help of CRISPR-Cas9 gene editing to knock out low-density lipoprotein receptor-related protein 4 (LRP4) in C28I2 and generate chondrocyte-specific Lrp4 knockout mice, the dependence of periplocin-mediated regulation of chondrocyte function on LRP4 was verified. This study not only provides new insights into understanding the chondroprotective effect of periplocin targeting LRP4 and its underlying mechanism but also offers experimental evidence for the use of periplocin as a potential disease-modifying OA drug (DMOAD) in OA treatment.