1. Academic Validation
  2. Immunomodulation Effects of Porcine Cartilage Acellularized Matrix (pCAM) for Osteoarthritis Treatment

Immunomodulation Effects of Porcine Cartilage Acellularized Matrix (pCAM) for Osteoarthritis Treatment

  • Tissue Eng Regen Med. 2025 Jan 9. doi: 10.1007/s13770-024-00687-5.
Ji Seob Kim # 1 Hyeon Jae Kwon # 2 In Sun Hwang 1 Young Hwa Lee 2 Kyung-Noh Yoon 2 Hee-Woong Yun 3 Jae-Hyeok Jang 1 Seo Jeong Kim 1 Zhoodatova Aiana 1 Seungwoo Kim 1 Minhee Moon 1 Bongki Kim 4 Byoung Ju Kim 5 Byung-Hyun Cha 6
Affiliations

Affiliations

  • 1 Division of Biomedical Convergence, College of Biomedical Science, Kangwon National University, Chuncheon-si, 24341, Republic of Korea.
  • 2 ATEMs, Research and Development Institute, Seoul, 05836, Republic of Korea.
  • 3 Department of Orthopedic Surgery, Ajou University School of Medicine, Suwon, 16499, Republic of Korea.
  • 4 Department of Animal Resources Science, Kongju National University, Yesan, 32439, Republic of Korea.
  • 5 ATEMs, Research and Development Institute, Seoul, 05836, Republic of Korea. kbz9861@hanmail.net.
  • 6 Division of Biomedical Convergence, College of Biomedical Science, Kangwon National University, Chuncheon-si, 24341, Republic of Korea. bhcha@kangwon.ac.kr.
  • # Contributed equally.
Abstract

Background: Pain reduction, immunomodulation, and cartilage repair are key therapeutic goals in osteoarthritis (OA) treatment. In this study, we evaluated the therapeutic effects of porcine cartilage acellularized matrix (pCAM) derived from naive tissue and compared it with the synthetic material polynucleotides (PN) for OA treatment.

Methods: pCAM was produced from porcine cartilage through physicochemical processing. LC-MS protein profiling identified the key proteins. In vitro experiments involved treating human synovial cell with pCAM and PN to assess cell viability and reductions in pro-inflammatory cytokines (IL-1β and IL-6). In vivo studies utilized a rat DMM-induced OA model. Pain was evaluated in weight-bearing tests, and inflammation reduction was confirmed using specific macrophage markers of CD68, CD86, and CD163 in immunohistochemical staining of synovial tissue. Cartilage regeneration was evaluated by histopathological analyses.

Results: The major protein components of pCAM include factors integral to cartilage and ECM integrity. They also contain proteins that help reduce inflammation. In vitro studies revealed a decrease in pro-inflammatory cytokines and survival of synovial cells were observed. In vivo treatment with pCAM resulted in a reduction of pain and inflammation, while promoting cartilage regeneration, thereby accelerating the healing process in OA.

Conclusion: Our findings suggest that pCAM may contribute to the treatment of OA by alleviating synovial inflammation and supporting cartilage regeneration, thereby addressing both the inflammatory and degenerative aspects of the disease.

Keywords

Decellularization; Extracellular Matrix; Immunomodulation; Osteoarthritis.

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