The Multifarious Functions of Leukotrienes in Bone Metabolism
| Main Author: | |
|---|---|
| Publication Date: | 2023 |
| Other Authors: | , , , , , , , , , , , , , , , , |
| Format: | Article |
| Language: | eng |
| Source: | Repositório Institucional da UNESP |
| Download full: | http://dx.doi.org/10.1002/jbmr.4867 https://hdl.handle.net/11449/307515 |
Summary: | Leukotrienes (LTs) are derived from arachidonic acid metabolism by the 5-lipoxygenase (5-LO) enzyme. The production of LTs is stimulated in the pathogenesis of rheumatoid arthritis (RA), osteoarthritis, and periodontitis, with a relevant contribution to bone resorption. However, its role in bone turnover, particularly the suppression of bone formation by modulating the function of osteoclasts and osteoblasts, remains unclear. We investigated the effects of LTs on bone metabolism and their impact on osteogenic differentiation and osteoclastogenesis using a 5-LO knockout (KO) mouse model. Results from micro-computed tomography (μCT) analysis of femur from 8-week-old 5-LO-deficient mice showed increased cortical bone and medullary region in females and males and decreased trabecular bone in females. In the vertebra, we observed increased marrow area in both females and males 5-LO KO and decreased trabecular bone only in females 5-LO KO. Immunohistochemistry (IHC) analysis showed higher levels of osteogenic markers tissue-nonspecific alkaline phosphatase (TNAP) and osteopontin (OPN) and lower expression of osteoclastogenic marker tartrate-resistant acid phosphatase (TRAP) in the femurs of 5-LO KO mice versus wild-type (WT). Alkaline phosphatase activity and mineralization assay results showed that the 5-LO absence enhances osteoblasts differentiation and mineralization but decreases the proliferation. Alkaline phosphatase (ALP), Bglap, and Sp7 gene expression were higher in 5-LO KO osteoblasts compared to WT cells. Eicosanoids production was higher in 5-LO KO osteoblasts except for thromboxane 2, which was lower in 5-LO–deficient mice. Proteomic analysis identified the downregulation of proteins related to adenosine triphosphate (ATP) metabolism in 5-LO KO osteoblasts, and the upregulation of transcription factors such as the adaptor-related protein complex 1 (AP-1 complex) in long bones from 5-LO KO mice leading to an increased bone formation pattern in 5-LO–deficient mice. We observed enormous differences in the morphology and function of osteoclasts with reduced bone resorption markers and impaired osteoclasts in 5-LO KO compared to WT osteoclasts. Altogether, these results demonstrate that the absence of 5-LO is related to the greater osteogenic profile. © 2023 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR). |
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The Multifarious Functions of Leukotrienes in Bone Metabolism5-LIPOXYGENASEBONE LOSSINFLAMMATORY DISEASESLEUKOTRIENESOSTEOBLASTSOSTEOCLASTOGENESISLeukotrienes (LTs) are derived from arachidonic acid metabolism by the 5-lipoxygenase (5-LO) enzyme. The production of LTs is stimulated in the pathogenesis of rheumatoid arthritis (RA), osteoarthritis, and periodontitis, with a relevant contribution to bone resorption. However, its role in bone turnover, particularly the suppression of bone formation by modulating the function of osteoclasts and osteoblasts, remains unclear. We investigated the effects of LTs on bone metabolism and their impact on osteogenic differentiation and osteoclastogenesis using a 5-LO knockout (KO) mouse model. Results from micro-computed tomography (μCT) analysis of femur from 8-week-old 5-LO-deficient mice showed increased cortical bone and medullary region in females and males and decreased trabecular bone in females. In the vertebra, we observed increased marrow area in both females and males 5-LO KO and decreased trabecular bone only in females 5-LO KO. Immunohistochemistry (IHC) analysis showed higher levels of osteogenic markers tissue-nonspecific alkaline phosphatase (TNAP) and osteopontin (OPN) and lower expression of osteoclastogenic marker tartrate-resistant acid phosphatase (TRAP) in the femurs of 5-LO KO mice versus wild-type (WT). Alkaline phosphatase activity and mineralization assay results showed that the 5-LO absence enhances osteoblasts differentiation and mineralization but decreases the proliferation. Alkaline phosphatase (ALP), Bglap, and Sp7 gene expression were higher in 5-LO KO osteoblasts compared to WT cells. Eicosanoids production was higher in 5-LO KO osteoblasts except for thromboxane 2, which was lower in 5-LO–deficient mice. Proteomic analysis identified the downregulation of proteins related to adenosine triphosphate (ATP) metabolism in 5-LO KO osteoblasts, and the upregulation of transcription factors such as the adaptor-related protein complex 1 (AP-1 complex) in long bones from 5-LO KO mice leading to an increased bone formation pattern in 5-LO–deficient mice. We observed enormous differences in the morphology and function of osteoclasts with reduced bone resorption markers and impaired osteoclasts in 5-LO KO compared to WT osteoclasts. Altogether, these results demonstrate that the absence of 5-LO is related to the greater osteogenic profile. © 2023 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).Endocrine Fellows FoundationMarie CurieCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Bauru School of Dentistry University of São Paulo, SPHuman Genetics Program Sanford Children's Health Research Center Sanford Burnham Prebys Medical Discovery InstituteInstitute for Regenerative Medicine University of ZürichRibeirão Preto Medical School University of São Paulo, SPInstitute of Biosciences São Paulo State University-UNESP, SPDepartment of Medicine University Center of Adamantina, SPDepartment of Medicine Faculdades de Dracena, SPSchool of Pharmaceutical Sciences of Ribeirão Preto University of São Paulo, SPInstitute of Biosciences São Paulo State University-UNESP, SPCAPES: 88881.030354/2013-01Universidade de São Paulo (USP)Sanford Burnham Prebys Medical Discovery InstituteUniversity of ZürichUniversidade Estadual Paulista (UNESP)University Center of AdamantinaFaculdades de DracenaAmadeu de Oliveira, FláviaTokuhara, Cintia K.Veeriah, VimalDomezi, João PauloSantesso, Mariana R.Cestari, Tania M.Ventura, Talita M.O.Matos, Adriana A.Dionísio, ThiagoFerreira, Marcel R. [UNESP]Ortiz, Rafael C.Duarte, Marco A.H.Buzalaf, Marília A.R.Ponce, José B.Sorgi, Carlos A.Faccioli, Lucia H.Buzalaf, Camila Peresde Oliveira, Rodrigo Cardoso2025-04-29T20:09:38Z2023-08-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1135-1153http://dx.doi.org/10.1002/jbmr.4867Journal of Bone and Mineral Research, v. 38, n. 8, p. 1135-1153, 2023.1523-46810884-0431https://hdl.handle.net/11449/30751510.1002/jbmr.48672-s2.0-85164128773Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Bone and Mineral Researchinfo:eu-repo/semantics/openAccess2025-04-30T14:36:44Zoai:repositorio.unesp.br:11449/307515Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462025-04-30T14:36:44Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
| dc.title.none.fl_str_mv |
The Multifarious Functions of Leukotrienes in Bone Metabolism |
| title |
The Multifarious Functions of Leukotrienes in Bone Metabolism |
| spellingShingle |
The Multifarious Functions of Leukotrienes in Bone Metabolism Amadeu de Oliveira, Flávia 5-LIPOXYGENASE BONE LOSS INFLAMMATORY DISEASES LEUKOTRIENES OSTEOBLASTS OSTEOCLASTOGENESIS |
| title_short |
The Multifarious Functions of Leukotrienes in Bone Metabolism |
| title_full |
The Multifarious Functions of Leukotrienes in Bone Metabolism |
| title_fullStr |
The Multifarious Functions of Leukotrienes in Bone Metabolism |
| title_full_unstemmed |
The Multifarious Functions of Leukotrienes in Bone Metabolism |
| title_sort |
The Multifarious Functions of Leukotrienes in Bone Metabolism |
| author |
Amadeu de Oliveira, Flávia |
| author_facet |
Amadeu de Oliveira, Flávia Tokuhara, Cintia K. Veeriah, Vimal Domezi, João Paulo Santesso, Mariana R. Cestari, Tania M. Ventura, Talita M.O. Matos, Adriana A. Dionísio, Thiago Ferreira, Marcel R. [UNESP] Ortiz, Rafael C. Duarte, Marco A.H. Buzalaf, Marília A.R. Ponce, José B. Sorgi, Carlos A. Faccioli, Lucia H. Buzalaf, Camila Peres de Oliveira, Rodrigo Cardoso |
| author_role |
author |
| author2 |
Tokuhara, Cintia K. Veeriah, Vimal Domezi, João Paulo Santesso, Mariana R. Cestari, Tania M. Ventura, Talita M.O. Matos, Adriana A. Dionísio, Thiago Ferreira, Marcel R. [UNESP] Ortiz, Rafael C. Duarte, Marco A.H. Buzalaf, Marília A.R. Ponce, José B. Sorgi, Carlos A. Faccioli, Lucia H. Buzalaf, Camila Peres de Oliveira, Rodrigo Cardoso |
| author2_role |
author author author author author author author author author author author author author author author author author |
| dc.contributor.none.fl_str_mv |
Universidade de São Paulo (USP) Sanford Burnham Prebys Medical Discovery Institute University of Zürich Universidade Estadual Paulista (UNESP) University Center of Adamantina Faculdades de Dracena |
| dc.contributor.author.fl_str_mv |
Amadeu de Oliveira, Flávia Tokuhara, Cintia K. Veeriah, Vimal Domezi, João Paulo Santesso, Mariana R. Cestari, Tania M. Ventura, Talita M.O. Matos, Adriana A. Dionísio, Thiago Ferreira, Marcel R. [UNESP] Ortiz, Rafael C. Duarte, Marco A.H. Buzalaf, Marília A.R. Ponce, José B. Sorgi, Carlos A. Faccioli, Lucia H. Buzalaf, Camila Peres de Oliveira, Rodrigo Cardoso |
| dc.subject.por.fl_str_mv |
5-LIPOXYGENASE BONE LOSS INFLAMMATORY DISEASES LEUKOTRIENES OSTEOBLASTS OSTEOCLASTOGENESIS |
| topic |
5-LIPOXYGENASE BONE LOSS INFLAMMATORY DISEASES LEUKOTRIENES OSTEOBLASTS OSTEOCLASTOGENESIS |
| description |
Leukotrienes (LTs) are derived from arachidonic acid metabolism by the 5-lipoxygenase (5-LO) enzyme. The production of LTs is stimulated in the pathogenesis of rheumatoid arthritis (RA), osteoarthritis, and periodontitis, with a relevant contribution to bone resorption. However, its role in bone turnover, particularly the suppression of bone formation by modulating the function of osteoclasts and osteoblasts, remains unclear. We investigated the effects of LTs on bone metabolism and their impact on osteogenic differentiation and osteoclastogenesis using a 5-LO knockout (KO) mouse model. Results from micro-computed tomography (μCT) analysis of femur from 8-week-old 5-LO-deficient mice showed increased cortical bone and medullary region in females and males and decreased trabecular bone in females. In the vertebra, we observed increased marrow area in both females and males 5-LO KO and decreased trabecular bone only in females 5-LO KO. Immunohistochemistry (IHC) analysis showed higher levels of osteogenic markers tissue-nonspecific alkaline phosphatase (TNAP) and osteopontin (OPN) and lower expression of osteoclastogenic marker tartrate-resistant acid phosphatase (TRAP) in the femurs of 5-LO KO mice versus wild-type (WT). Alkaline phosphatase activity and mineralization assay results showed that the 5-LO absence enhances osteoblasts differentiation and mineralization but decreases the proliferation. Alkaline phosphatase (ALP), Bglap, and Sp7 gene expression were higher in 5-LO KO osteoblasts compared to WT cells. Eicosanoids production was higher in 5-LO KO osteoblasts except for thromboxane 2, which was lower in 5-LO–deficient mice. Proteomic analysis identified the downregulation of proteins related to adenosine triphosphate (ATP) metabolism in 5-LO KO osteoblasts, and the upregulation of transcription factors such as the adaptor-related protein complex 1 (AP-1 complex) in long bones from 5-LO KO mice leading to an increased bone formation pattern in 5-LO–deficient mice. We observed enormous differences in the morphology and function of osteoclasts with reduced bone resorption markers and impaired osteoclasts in 5-LO KO compared to WT osteoclasts. Altogether, these results demonstrate that the absence of 5-LO is related to the greater osteogenic profile. © 2023 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR). |
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2023 |
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2023-08-01 2025-04-29T20:09:38Z |
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info:eu-repo/semantics/publishedVersion |
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info:eu-repo/semantics/article |
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article |
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publishedVersion |
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http://dx.doi.org/10.1002/jbmr.4867 Journal of Bone and Mineral Research, v. 38, n. 8, p. 1135-1153, 2023. 1523-4681 0884-0431 https://hdl.handle.net/11449/307515 10.1002/jbmr.4867 2-s2.0-85164128773 |
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http://dx.doi.org/10.1002/jbmr.4867 https://hdl.handle.net/11449/307515 |
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Journal of Bone and Mineral Research, v. 38, n. 8, p. 1135-1153, 2023. 1523-4681 0884-0431 10.1002/jbmr.4867 2-s2.0-85164128773 |
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eng |
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Journal of Bone and Mineral Research |
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openAccess |
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