Downloads
Download
Additional Files
Download - Supplementary Materials
This work is licensed under a Creative Commons Attribution 4.0 International License.
Article
Intravenous Transplantation of Apoptosis Repressor with Caspase Recruitment Domain-Overexpressing Mesenchymal Stem Cells Promotes Bone Formation in Bisphosphonate-Related Osteonecrosis of the Jaw Rats
Ruixue Jiang 1,2,†, Yuwei Deng 1,2,†, Yuhui Zhu 1,2, Jin Wen 1,2, Xinquan Jiang 1,2,* and Longwei Hu 2,3,*
1 Department of Prosthodontics, Ninth People’s Hospital affiliated to Shanghai Jiao Tong University School of Medicine, 639 Zhizaoju Road, Shanghai 200011, China
2 Shanghai Engineering Research Center of Advanced Dental Technology and Materials, Shanghai Key Laboratory of Stomatology & Shanghai Research Institute of Stomatology, National Clinical Research Center for Oral Diseases, Shanghai Ninth People’s Hospital, College of Stomatology, Shanghai Jiao Tong University School of Medicine, 639 Zhizaoju Road, Shanghai 200011, China
3 Department of Oral & Maxillofacial-Head & Neck Oncology, Ninth People’s Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, 639 Zhizaoju Road, Shanghai 200011, China
* Correspondence: xinquanjiang@aliyun.com (X.J.); 121009@sh9hospital.org.cn (L.H.)
† These authors contributed equally to this work.
Received: 18 October 2024; Revised: 17 November 2024; Accepted: 20 November 2024; Published: 29 November 2024
Abstract: Bisphosphonate-related osteonecrosis of the jaw (BRONJ) is a serious complication caused by the application of bisphosphonates (BPs) which are widely used in bone metastasis, osteoporosis and other metabolic bone diseases. Since bone marrow-derived mesenchymal stem cells (BMSCs) dysfunction potentially plays a critical role in the development of BRONJ, purposefully improving the function of BMSCs may help reduce the symptoms of BRONJ. Apoptosis repressor with caspase recruitment domain (ARC) can inhibit cell apoptosis and cell death, and was confirmed to possess an obvious reparative function in damaged tissues recently. Therefore, we aimed to investigate whether transplantation of ARC-overexpressing BMSCs had a therapeutic effect on BRONJ and explored possible mechanisms. First, we successfully established the BRONJ rat model and confirmed that BRONJ-derived BMSCs showed decreased proliferation and osteogenic differentiation ability. However, ARC-overexpressing BMSCs showed a significant therapeutic effect on BRONJ by promoting osteogenesis and inhibiting osteoclasts. The BRONJ tissue treated with ARC-overexpressing BMSCs also showed a decreased level of cell apoptosis. Further the RNA sequencing and bioinformatics results suggested that ARC can regulate BMSCs by inhibiting the TNF-α (tumor necrosis factor-α) pathway increased in the BRONJ samples and may alleviate the disease by reducing pro-inflammatory potential of BRONJ-derived BMSCs. In summary, ARC-overexpressing BMSCs can effectively repair BRONJ necrotic bone tissue which provides new ideas for the clinical treatment of BRONJ.
Keywords:
bisphosphonate-related osteonecrosis of the jaw apoptosis repressor with caspase recruitment domain bone marrow stem cells stem cell transplantation bone microenvironmentReferences
- Yarom, N.; Shapiro, C.L.; Peterson, D.E.; Van Poznak, C.H.; Bohlke, K.; Ruggiero, S.L.; Saunders, D.P. Medication-Related Osteonecrosis of the Jaw: MASCC/ISOO/ASCO Clinical Practice Guideline. J. Clin. Oncol. 2019, 37, 2270–2290.
- Ruggiero, S.L.; Dodson, T.B.; Fantasia, J.; Goodday, R.; Aghaloo, T.; Mehrotra, B.; O’Ryan, F. American Association of Oral and Maxillofacial Surgeons position paper on medication-related osteonecrosis of the jaw-2014 update. J. Oral. Maxillofac. Surg. 2014, 72, 193 8–1956.
- Khan, A.A.; Morrison, A.; Hanley, D.A.; Felsenberg, D.; McCauley, L.K.; O’Ryan, F.; International Task Force on Osteonecrosis of the Jaw. Diagnosis and management of osteonecrosis of the jaw: A systematic review and international consensus. J. Bone Miner. Res. 2015, 30, 3–23.
- Nicolatou-Galitis, O.; Schiødt, M.; Mendes, R.A.; Ripamonti, C.; Hope, S.; Drudge-Coates, L.; Van den Wyngaert, T. Medication-related osteonecrosis of the jaw: Definition and best practice for prevention, diagnosis, and treatment. Oral. Surg. Oral. Med. Oral. Pathol. Oral. Radiol. 2019, 127, 117–135.
- Gross, C.; Weber, M.; Creutzburg, K.; Möbius, P.; Preidl, R.; Amann, K.; Wehrhan, F. Osteoclast profile of medication-related osteonecrosis of the jaw secondary to bisphosphonate therapy: A comparison with osteoradionecrosis and osteomyelitis. J. Transl. Med. 2017, 15, 128.
- Kuroshima, S.; Sasaki, M.; Murata, H.; Sawase, T. Medication-related osteonecrosis of the jaw-like lesions in rodents: A comprehensive systematic review and meta-analysis. Gerodontology 2019, 36, 313–324.
- Li, Y.; Xu, J.; Mao, L.; Liu, Y.; Gao, R.; Zheng, Z.; Wang, S. Allogeneic mesenchymal stem cell therapy for bisphosphonate-related jaw osteonecrosis in Swine. Stem Cells Dev. 2013, 22, 2047–2056.
- Shi, Y.; Wang, Y.; Li, Q.; Liu, K.; Hou, J.; Shao, C.; Wang, Y. Immunoregulatory mechanisms of mesenchymal stem and stromal cells in inflammatory diseases. Nat. Rev. Nephrol. 2018, 14, 493–507.
- Jiang, Y.; Zhang, P.; Zhang, X.; Lv, L.; Zhou, Y. Advances in mesenchymal stem cell transplantation for the treatment of osteoporosis. Cell Prolif. 2021, 54, e12956.
- Yang, M.; Chen, J.; Chen, L. The roles of mesenchymal stem cell-derived exosomes in diabetes mellitus and its related complications. Front. Endocrinol. (Lausanne) 2022, 13, 1027686.
- Rodríguez-Lozano, F.J.; Oñate-Sánchez, R.; Gonzálvez-García, M.; Vallés-Bergadá; M; Martínez, C.M.; Revilla-Nuin, B.; García-Bernal, D. Allogeneic Bone Marrow Mesenchymal Stem Cell Transplantation in Tooth Extractions Sites Ameliorates the Incidence of Osteonecrotic Jaw-Like Lesions in Zoledronic Acid-Treated Rats. J. Clin. Med. 2020, 9, 1649.
- Kaibuchi, N.; Iwata, T.; Onizuka, S.; Yano, K.; Tsumanuma, Y.; Yamato, M.; Ando, T. Allogeneic multipotent mesenchymal stromal cell sheet transplantation promotes healthy healing of wounds caused by zoledronate and dexamethasone in canine mandibular bones. Regen. Ther. 2019, 10, 77–83.
- Matsuura, Y.; Atsuta, I.; Ayukawa, Y.; Yamaza, T.; Kondo, R.; Takahashi, A.; Koyano, K. Therapeutic interactions between mesenchymal stem cells for healing medication-related osteonecrosis of the jaw. Stem Cell Res. Ther. 2016, 7, 119.
- Hu, L.; Wang, Y.; Pan, H.; Kadir, K.; Wen, J.; Li, S.; Zhang, C. Apoptosis repressor with caspase recruitment domain (ARC) promotes bone regeneration of bone marrow-derived mesenchymal stem cells by activating Fgf-2/PI3K/Akt signaling. Stem Cell Res. Ther. 2021, 12, 185.
- Zou, D.; Zhang, Z.; He, J.; Zhu, S.; Wang, S.; Zhang, W.; Huang, Y. Repairing critical-sized calvarial defects with BMSCs modified by a constitutively active form of hypoxia-inducible factor-1 alpha and a phosphate cement scaffold. Biomaterials 2011, 32, 9707–9718.
- Shao, H.; Shen, J.; Wang, M.; Cui, J.; Wang, Y.; Zhu, S.; Geng, D. Icariin protects against titanium particle-induced osteolysis and inflammatory response in a mouse calvarial model. Biomaterials 2015, 60, 92–99.
- Tsukasaki, M.; Takayanagi, H. Osteoimmunology: Evolving concepts in bone-immune interactions in health and disease. Nat. Rev. Immunol. 2019, 19, 626–642.
- Ogata, K.; Matsumura, M.; Moriyama, M.; Katagiri, W.; Hibi, H.; Nakamura, S. Cytokine Mixtures Mimicking Secretomes from Mesenchymal Stem Cells Improve Medication-Related Osteonecrosis of the Jaw in a Rat Model. JBMR Plus 2018, 2, 69–80.
- Hu, L.; Han, J.; Yang, X.; Wang, Y.; Pan, H.; Xu, L. Apoptosis repressor with caspase recruitment domain enhances survival and promotes osteogenic differentiation of human osteoblast cells under Zoledronate treatment. Mol. Med. Rep. 2016, 14, 3535–3542.
- He, D.; Liu, F.; Cui, S.; Jiang, N.; Yu, H.; Zhou, Y.; Kou, X. Mechanical load-induced HS production by periodontal ligament stem cells activates M1 macrophages to promote bone remodeling and tooth movement via STAT1. Stem Cell Res. Ther. 2020, 11, 112.
- Metzger, C.E.; Narayanan, S.A. The Role of Osteocytes in Inflammatory Bone Loss. Front. Endocrinol. (Lausanne) 2019, 10, 285.
- Le Blanc, K.; Rasmusson, I.; Sundberg, B.; Götherström, C.; Hassan, M.; Uzunel, M.; Ringdén, O. Treatment of severe acute graft-versus-host disease with third party haploidentical mesenchymal stem cells. Lancet 2004, 363, 1439–1441.