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Nitrogen-Containing Bisphosphonates Downregulate Cathepsin K and Upregulate Annexin V in Osteoclasts Cultured In Vitro

INTRODUCTION: Bisphosphonates are widely used in the treatment of osteoporosis; however, they are associated with the serious adverse event of bisphosphonate‐related osteonecrosis of the jaw (BRONJ). AIM: The aim of this study is to assess the effects of nitrogen-containing bisphosphonates (N-PHs) o...

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Autores principales: Bautista-Carbajal, Arturo, Villanueva-Arriaga, Rosina Eugenia, Páez-Arenas, Araceli, Massó-Rojas, Felipe, Frechero Molina, Nelly, García-López, Salvador
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9974278/
https://www.ncbi.nlm.nih.gov/pubmed/36866025
http://dx.doi.org/10.1155/2023/2960941
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author Bautista-Carbajal, Arturo
Villanueva-Arriaga, Rosina Eugenia
Páez-Arenas, Araceli
Massó-Rojas, Felipe
Frechero Molina, Nelly
García-López, Salvador
author_facet Bautista-Carbajal, Arturo
Villanueva-Arriaga, Rosina Eugenia
Páez-Arenas, Araceli
Massó-Rojas, Felipe
Frechero Molina, Nelly
García-López, Salvador
author_sort Bautista-Carbajal, Arturo
collection PubMed
description INTRODUCTION: Bisphosphonates are widely used in the treatment of osteoporosis; however, they are associated with the serious adverse event of bisphosphonate‐related osteonecrosis of the jaw (BRONJ). AIM: The aim of this study is to assess the effects of nitrogen-containing bisphosphonates (N-PHs) on the synthesis of IL-1β, TNF-α, sRANKL, cathepsin K, and annexin V in bone cells cultured in vitro. MATERIALS AND METHODS: Osteoblasts and bone marrow-derived osteoclasts were cultured in vitro, subjected to treatment with alendronate, risedronate, or ibandronate at a concentration of 10(−5) M for 0 to 96 h and then assayed for IL-1β, sRANKL, and TNF-α production by ELISA. Cathepsin K and Annexin V-FITC staining in osteoclasts were assessed by flow cytometry. RESULTS: There was significant downregulation of IL-1β, sRANKL, and TNF-α in experimental osteoblasts compared to control cells, and there was upregulation of IL-1β and downregulation of RANKL and TNF-α in experimental osteoclasts. Furthermore, in osteoclasts, cathepsin K expression was downregulated at 48–72 h with alendronate treatment, while risedronate treatment resulted in upregulated annexin V expression at 48 h compared to the control treatment. CONCLUSION: Bisphosphonates added to bone cells inhibited osteoclastogenesis, which led to the downregulation of cathepsin K and induction of apoptosis in osteoclasts; these changes limited the capacity of bone remodelling and healing that may contribute to BRONJ induced by surgical dental procedures.
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spelling pubmed-99742782023-03-01 Nitrogen-Containing Bisphosphonates Downregulate Cathepsin K and Upregulate Annexin V in Osteoclasts Cultured In Vitro Bautista-Carbajal, Arturo Villanueva-Arriaga, Rosina Eugenia Páez-Arenas, Araceli Massó-Rojas, Felipe Frechero Molina, Nelly García-López, Salvador Int J Dent Research Article INTRODUCTION: Bisphosphonates are widely used in the treatment of osteoporosis; however, they are associated with the serious adverse event of bisphosphonate‐related osteonecrosis of the jaw (BRONJ). AIM: The aim of this study is to assess the effects of nitrogen-containing bisphosphonates (N-PHs) on the synthesis of IL-1β, TNF-α, sRANKL, cathepsin K, and annexin V in bone cells cultured in vitro. MATERIALS AND METHODS: Osteoblasts and bone marrow-derived osteoclasts were cultured in vitro, subjected to treatment with alendronate, risedronate, or ibandronate at a concentration of 10(−5) M for 0 to 96 h and then assayed for IL-1β, sRANKL, and TNF-α production by ELISA. Cathepsin K and Annexin V-FITC staining in osteoclasts were assessed by flow cytometry. RESULTS: There was significant downregulation of IL-1β, sRANKL, and TNF-α in experimental osteoblasts compared to control cells, and there was upregulation of IL-1β and downregulation of RANKL and TNF-α in experimental osteoclasts. Furthermore, in osteoclasts, cathepsin K expression was downregulated at 48–72 h with alendronate treatment, while risedronate treatment resulted in upregulated annexin V expression at 48 h compared to the control treatment. CONCLUSION: Bisphosphonates added to bone cells inhibited osteoclastogenesis, which led to the downregulation of cathepsin K and induction of apoptosis in osteoclasts; these changes limited the capacity of bone remodelling and healing that may contribute to BRONJ induced by surgical dental procedures. Hindawi 2023-02-21 /pmc/articles/PMC9974278/ /pubmed/36866025 http://dx.doi.org/10.1155/2023/2960941 Text en Copyright © 2023 Arturo Bautista-Carbajal et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Bautista-Carbajal, Arturo
Villanueva-Arriaga, Rosina Eugenia
Páez-Arenas, Araceli
Massó-Rojas, Felipe
Frechero Molina, Nelly
García-López, Salvador
Nitrogen-Containing Bisphosphonates Downregulate Cathepsin K and Upregulate Annexin V in Osteoclasts Cultured In Vitro
title Nitrogen-Containing Bisphosphonates Downregulate Cathepsin K and Upregulate Annexin V in Osteoclasts Cultured In Vitro
title_full Nitrogen-Containing Bisphosphonates Downregulate Cathepsin K and Upregulate Annexin V in Osteoclasts Cultured In Vitro
title_fullStr Nitrogen-Containing Bisphosphonates Downregulate Cathepsin K and Upregulate Annexin V in Osteoclasts Cultured In Vitro
title_full_unstemmed Nitrogen-Containing Bisphosphonates Downregulate Cathepsin K and Upregulate Annexin V in Osteoclasts Cultured In Vitro
title_short Nitrogen-Containing Bisphosphonates Downregulate Cathepsin K and Upregulate Annexin V in Osteoclasts Cultured In Vitro
title_sort nitrogen-containing bisphosphonates downregulate cathepsin k and upregulate annexin v in osteoclasts cultured in vitro
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9974278/
https://www.ncbi.nlm.nih.gov/pubmed/36866025
http://dx.doi.org/10.1155/2023/2960941
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