Functional alterations in mechanical loading of condylar cartilage induces changes in the bony subcondylar region
Bone remodeling is orchestrated by cells of the osteoblast lineage and involves an intricate network of cell–cell and cell–matrix interactions. This dynamic process engages systemic hormones, locally produced cytokines and growth factors, as well as the mechanical environment of the cells. In growin...
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Published in | Archives of oral biology Vol. 54; no. 11; pp. 1035 - 1045 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Elsevier Ltd
01.11.2009
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Subjects | |
Online Access | Get full text |
ISSN | 0003-9969 1879-1506 1879-1506 |
DOI | 10.1016/j.archoralbio.2009.08.010 |
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Abstract | Bone remodeling is orchestrated by cells of the osteoblast lineage and involves an intricate network of cell–cell and cell–matrix interactions. This dynamic process engages systemic hormones, locally produced cytokines and growth factors, as well as the mechanical environment of the cells. In growing subjects, the mandibular condyle consists of both articular and growth components and the presence of progenitor cells is verified by their anabolic responses to growth hormones. The pathways of chondrocyte and osteoblast differentiation during endochondral bone formation are interconnected and controlled by key transcription factors. The present study was undertaken to explore the possibility and the extent by which the mechano-transduction events in chondrocytes are ‘sensed’ in the subchondral bony area under altered functional loading. To this end, the involvement of the JNK/ERK–AP-1/Runx2 signaling axe was investigated by immunohistochemistry in temporomandibular joints of young rats subjected to different functional mastication loads. Our results showed that mechanical load triggers differentiation phenomena through the induction of master tissue regulators, namely the expression and/or activation of the JNK–c-Jun signaling pathway components and c-Fos in subchondral osteoblasts, as well as the activation of ERK/MAPK and the cellular expression of the transcription factor Runx2 in subchondral osteoblasts. |
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AbstractList | Bone remodeling is orchestrated by cells of the osteoblast lineage and involves an intricate network of cell–cell and cell–matrix interactions. This dynamic process engages systemic hormones, locally produced cytokines and growth factors, as well as the mechanical environment of the cells. In growing subjects, the mandibular condyle consists of both articular and growth components and the presence of progenitor cells is verified by their anabolic responses to growth hormones. The pathways of chondrocyte and osteoblast differentiation during endochondral bone formation are interconnected and controlled by key transcription factors. The present study was undertaken to explore the possibility and the extent by which the mechano-transduction events in chondrocytes are ‘sensed’ in the subchondral bony area under altered functional loading. To this end, the involvement of the JNK/ERK–AP-1/Runx2 signaling axe was investigated by immunohistochemistry in temporomandibular joints of young rats subjected to different functional mastication loads. Our results showed that mechanical load triggers differentiation phenomena through the induction of master tissue regulators, namely the expression and/or activation of the JNK–c-Jun signaling pathway components and c-Fos in subchondral osteoblasts, as well as the activation of ERK/MAPK and the cellular expression of the transcription factor Runx2 in subchondral osteoblasts. Abstract Bone remodeling is orchestrated by cells of the osteoblast lineage and involves an intricate network of cell–cell and cell–matrix interactions. This dynamic process engages systemic hormones, locally produced cytokines and growth factors, as well as the mechanical environment of the cells. In growing subjects, the mandibular condyle consists of both articular and growth components and the presence of progenitor cells is verified by their anabolic responses to growth hormones. The pathways of chondrocyte and osteoblast differentiation during endochondral bone formation are interconnected and controlled by key transcription factors. The present study was undertaken to explore the possibility and the extent by which the mechano-transduction events in chondrocytes are ‘sensed’ in the subchondral bony area under altered functional loading. To this end, the involvement of the JNK/ERK–AP-1/Runx2 signaling axe was investigated by immunohistochemistry in temporomandibular joints of young rats subjected to different functional mastication loads. Our results showed that mechanical load triggers differentiation phenomena through the induction of master tissue regulators, namely the expression and/or activation of the JNK–c-Jun signaling pathway components and c-Fos in subchondral osteoblasts, as well as the activation of ERK/MAPK and the cellular expression of the transcription factor Runx2 in subchondral osteoblasts. Bone remodeling is orchestrated by cells of the osteoblast lineage and involves an intricate network of cell-cell and cell-matrix interactions. This dynamic process engages systemic hormones, locally produced cytokines and growth factors, as well as the mechanical environment of the cells. In growing subjects, the mandibular condyle consists of both articular and growth components and the presence of progenitor cells is verified by their anabolic responses to growth hormones. The pathways of chondrocyte and osteoblast differentiation during endochondral bone formation are interconnected and controlled by key transcription factors. The present study was undertaken to explore the possibility and the extent by which the mechano-transduction events in chondrocytes are 'sensed' in the subchondral bony area under altered functional loading. To this end, the involvement of the JNK/ERK-AP-1/Runx2 signaling axe was investigated by immunohistochemistry in temporomandibular joints of young rats subjected to different functional mastication loads. Our results showed that mechanical load triggers differentiation phenomena through the induction of master tissue regulators, namely the expression and/or activation of the JNK-c-Jun signaling pathway components and c-Fos in subchondral osteoblasts, as well as the activation of ERK/MAPK and the cellular expression of the transcription factor Runx2 in subchondral osteoblasts.Bone remodeling is orchestrated by cells of the osteoblast lineage and involves an intricate network of cell-cell and cell-matrix interactions. This dynamic process engages systemic hormones, locally produced cytokines and growth factors, as well as the mechanical environment of the cells. In growing subjects, the mandibular condyle consists of both articular and growth components and the presence of progenitor cells is verified by their anabolic responses to growth hormones. The pathways of chondrocyte and osteoblast differentiation during endochondral bone formation are interconnected and controlled by key transcription factors. The present study was undertaken to explore the possibility and the extent by which the mechano-transduction events in chondrocytes are 'sensed' in the subchondral bony area under altered functional loading. To this end, the involvement of the JNK/ERK-AP-1/Runx2 signaling axe was investigated by immunohistochemistry in temporomandibular joints of young rats subjected to different functional mastication loads. Our results showed that mechanical load triggers differentiation phenomena through the induction of master tissue regulators, namely the expression and/or activation of the JNK-c-Jun signaling pathway components and c-Fos in subchondral osteoblasts, as well as the activation of ERK/MAPK and the cellular expression of the transcription factor Runx2 in subchondral osteoblasts. |
Author | Papachristou, Dionysios J. Pirttiniemi, Pertti Basdra, Efthimia K. Papavassiliou, George A. Papachroni, Katerina K. Gorgoulis, Vassilis G. Piperi, Christina |
Author_xml | – sequence: 1 givenname: Dionysios J. surname: Papachristou fullname: Papachristou, Dionysios J. organization: Department of Pathology, University of Pittsburgh Medical Center, Pittsburgh, PA, USA – sequence: 2 givenname: Katerina K. surname: Papachroni fullname: Papachroni, Katerina K. organization: Department of Biological Chemistry, University of Athens Medical School, Athens, Greece – sequence: 3 givenname: George A. surname: Papavassiliou fullname: Papavassiliou, George A. organization: 129 Franklin Str., Cambridge, MA, USA – sequence: 4 givenname: Pertti surname: Pirttiniemi fullname: Pirttiniemi, Pertti organization: Institutes of Dentistry, University of Oulu, Oulu, Finland – sequence: 5 givenname: Vassilis G. surname: Gorgoulis fullname: Gorgoulis, Vassilis G. organization: Department of Histology and Embryology, Cellular and Molecular Biomechanics Unit, University of Athens Medical School, 75 M. Asias Str., 11527 Athens, Greece – sequence: 6 givenname: Christina surname: Piperi fullname: Piperi, Christina organization: Department of Biological Chemistry, University of Athens Medical School, Athens, Greece – sequence: 7 givenname: Efthimia K. surname: Basdra fullname: Basdra, Efthimia K. email: ebasdra@med.uoa.gr organization: Department of Histology and Embryology, Cellular and Molecular Biomechanics Unit, University of Athens Medical School, 75 M. Asias Str., 11527 Athens, Greece |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/19775676$$D View this record in MEDLINE/PubMed |
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Snippet | Bone remodeling is orchestrated by cells of the osteoblast lineage and involves an intricate network of cell–cell and cell–matrix interactions. This dynamic... Abstract Bone remodeling is orchestrated by cells of the osteoblast lineage and involves an intricate network of cell–cell and cell–matrix interactions. This... Bone remodeling is orchestrated by cells of the osteoblast lineage and involves an intricate network of cell-cell and cell-matrix interactions. This dynamic... |
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SubjectTerms | Advanced Basic Science Animals Bite Force Bone collar Bone Remodeling - physiology Cartilage, Articular - physiology Cell Differentiation Chondrocytes - physiology Core Binding Factor Alpha 1 Subunit - biosynthesis Dental Stress Analysis Dentistry Female Gene Expression Regulation, Developmental Logistic Models Mandibular Condyle - physiology MAP Kinase Signaling System Mastication - physiology Mechanical load Osteoblasts - metabolism Rats Rats, Wistar Runx2 Temporomandibular joint Temporomandibular Joint - physiology Transcription Factor AP-1 - biosynthesis |
Title | Functional alterations in mechanical loading of condylar cartilage induces changes in the bony subcondylar region |
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