Cryopreservation induces macrophage colony stimulating factor from human periodontal ligament cells in vitro
Cryopreservation is used to protect vital periodontal ligaments during the transplantation of teeth. We investigated which gene products implicated in root resorption are upregulated in human periodontal ligament cells by cryopreservation, and whether cryopreservation affects the expression of macro...
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| Published in: | Cryobiology Vol. 67; no. 2; pp. 156 - 162 |
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| Abstract | Cryopreservation is used to protect vital periodontal ligaments during the transplantation of teeth. We investigated which gene products implicated in root resorption are upregulated in human periodontal ligament cells by cryopreservation, and whether cryopreservation affects the expression of macrophage-colony stimulating factor (M-CSF) in human periodontal ligament cells. We used customized microarrays to compare gene expression in human periodontal ligament cells cultured from teeth immediately after extraction and from cryopreserved teeth. Based on the result of these assays, we examined M-CSF expression in periodontal ligament cells from the immediately extracted tooth and cryopreserved teeth by real-time PCR, enzyme-linked immunosorbent assay (ELISA), Western blot analysis, and immunofluorescence. We also investigated whether human bone marrow cells differentiate into tartrate-resistant acid phosphatase (TRAP) positive osteoclasts when stimulated with RANKL (Receptor Activator for Nuclear Factor κ B Ligand) together with any secreted M-CSF present in the supernatants of the periodontal ligament cells cultured from the various groups of teeth. M-CSF was twofold higher in the periodontal ligament cells from the rapid freezing teeth than in those from the immediately extracted group (p<0.05). Cryopreservation increased M-CSF expression in the periodontal ligament cells when analyzed by real time PCR, ELISA, Western blotting, and immunofluorescence (p<0.05). TRAP positive osteoclasts were formed in response to RANKL and the secreted M-CSF present in the supernatants of all the experimental groups except negative control. These results demonstrate that cryopreservation promotes the production of M-CSF, which plays an important role in root resorption by periodontal ligament cells. |
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| AbstractList | Cryopreservation is used to protect vital periodontal ligaments during the transplantation of teeth. We investigated which gene products implicated in root resorption are upregulated in human periodontal ligament cells by cryopreservation, and whether cryopreservation affects the expression of macrophage-colony stimulating factor (M-CSF) in human periodontal ligament cells. We used customized microarrays to compare gene expression in human periodontal ligament cells cultured from teeth immediately after extraction and from cryopreserved teeth. Based on the result of these assays, we examined M-CSF expression in periodontal ligament cells from the immediately extracted tooth and cryopreserved teeth by real-time PCR, enzyme-linked immunosorbent assay (ELISA), Western blot analysis, and immunofluorescence. We also investigated whether human bone marrow cells differentiate into tartrate-resistant acid phosphatase (TRAP) positive osteoclasts when stimulated with RANKL (Receptor Activator for Nuclear Factor κ B Ligand) together with any secreted M-CSF present in the supernatants of the periodontal ligament cells cultured from the various groups of teeth. M-CSF was twofold higher in the periodontal ligament cells from the rapid freezing teeth than in those from the immediately extracted group (p<0.05). Cryopreservation increased M-CSF expression in the periodontal ligament cells when analyzed by real time PCR, ELISA, Western blotting, and immunofluorescence (p<0.05). TRAP positive osteoclasts were formed in response to RANKL and the secreted M-CSF present in the supernatants of all the experimental groups except negative control. These results demonstrate that cryopreservation promotes the production of M-CSF, which plays an important role in root resorption by periodontal ligament cells. Cryopreservation is used to protect vital periodontal ligaments during the transplantation of teeth. We investigated which gene products implicated in root resorption are upregulated in human periodontal ligament cells by cryopreservation, and whether cryopreservation affects the expression of macrophage-colony stimulating factor (M-CSF) in human periodontal ligament cells. We used customized microarrays to compare gene expression in human periodontal ligament cells cultured from teeth immediately after extraction and from cryopreserved teeth. Based on the result of these assays, we examined M-CSF expression in periodontal ligament cells from the immediately extracted tooth and cryopreserved teeth by real-time PCR, enzyme-linked immunosorbent assay (ELISA), Western blot analysis, and immunofluorescence. We also investigated whether human bone marrow cells differentiate into tartrate-resistant acid phosphatase (TRAP) positive osteoclasts when stimulated with RANKL (Receptor Activator for Nuclear Factor κ B Ligand) together with any secreted M-CSF present in the supernatants of the periodontal ligament cells cultured from the various groups of teeth. M-CSF was twofold higher in the periodontal ligament cells from the rapid freezing teeth than in those from the immediately extracted group (p < 0.05). Cryopreservation increased M-CSF expression in the periodontal ligament cells when analyzed by real time PCR, ELISA, Western blotting, and immunofluorescence (p < 0.05). TRAP positive osteoclasts were formed in response to RANKL and the secreted M-CSF present in the supernatants of all the experimental groups except negative control. These results demonstrate that cryopreservation promotes the production of M-CSF, which plays an important role in root resorption by periodontal ligament cells. Cryopreservation is used to protect vital periodontal ligaments during the transplantation of teeth. We investigated which gene products implicated in root resorption are upregulated in human periodontal ligament cells by cryopreservation, and whether cryopreservation affects the expression of macrophage-colony stimulating factor (M-CSF) in human periodontal ligament cells. We used customized microarrays to compare gene expression in human periodontal ligament cells cultured from teeth immediately after extraction and from cryopreserved teeth. Based on the result of these assays, we examined M-CSF expression in periodontal ligament cells from the immediately extracted tooth and cryopreserved teeth by real-time PCR, enzyme-linked immunosorbent assay (ELISA), Western blot analysis, and immunofluorescence. We also investigated whether human bone marrow cells differentiate into tartrate-resistant acid phosphatase (TRAP) positive osteoclasts when stimulated with RANKL (Receptor Activator for Nuclear Factor Kappa B Ligand) together with any secreted M-CSF present in the supernatants of the periodontal ligament cells cultured from the various groups of teeth. M-CSF was twofold higher in the periodontal ligament cells from the rapid freezing teeth than in those from the immediately extracted group (p <0.05). Cryopreservation increased M-CSF expression in the periodontal ligament cells when analyzed by real time PCR, ELISA, Western blotting, and immunofluorescence (p <0.05). TRAP positive osteoclasts were formed in response to RANKL and the secreted M-CSF present in the supernatants of all the experimental groups except negative control. These results demonstrate that cryopreservation promotes the production of M-CSF, which plays an important role in root resorption by periodontal ligament cells. |
| Author | Kim, J.-Y. Jung, S.-H. Ahn, S.-J. Lee, H.-W. Kim, K.-H. Kim, E.-C. Park, S.-H. Rhim, E.-M. Chang, Y.-R. |
| Author_xml | – sequence: 1 givenname: E.-M. surname: Rhim fullname: Rhim, E.-M. organization: Department of Conservative Dentistry, St. Paul’s Hospital, Seoul, South Korea – sequence: 2 givenname: S.-J. surname: Ahn fullname: Ahn, S.-J. organization: Kyung Hee University Dental Hospital at Gangdong, Seoul, South Korea – sequence: 3 givenname: J.-Y. surname: Kim fullname: Kim, J.-Y. organization: Department of Conservative Dentistry, Graduate School, Kyung Hee University, Seoul, South Korea – sequence: 4 givenname: Y.-R. surname: Chang fullname: Chang, Y.-R. organization: Department of Conservative Dentistry, Graduate School, Kyung Hee University, Seoul, South Korea – sequence: 5 givenname: K.-H. surname: Kim fullname: Kim, K.-H. organization: Kyung Hee University Dental Hospital at Gangdong, Seoul, South Korea – sequence: 6 givenname: H.-W. surname: Lee fullname: Lee, H.-W. organization: Oral Biology Research Institute, School of Dentistry, Kyung Hee University, Seoul, South Korea – sequence: 7 givenname: S.-H. surname: Jung fullname: Jung, S.-H. organization: Kyung Hee University Dental Hospital at Gangdong, Seoul, South Korea – sequence: 8 givenname: E.-C. surname: Kim fullname: Kim, E.-C. email: eckim@khu.ac.kr organization: Oral Biology Research Institute, School of Dentistry, Kyung Hee University, Seoul, South Korea – sequence: 9 givenname: S.-H. surname: Park fullname: Park, S.-H. email: shpark94@khu.ac.kr organization: Kyung Hee University Dental Hospital at Gangdong, Seoul, South Korea |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/23810633$$D View this record in MEDLINE/PubMed |
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| Keywords | Root resorption Periodontal ligament cells Quantitative real-time polymerase chain reaction Macrophage colony-stimulating factor Osteoclast Freezing Western blotting Microarray analysis ELISA |
| Language | English |
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| Snippet | Cryopreservation is used to protect vital periodontal ligaments during the transplantation of teeth. We investigated which gene products implicated in root... |
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| SubjectTerms | Bone Marrow Cells - cytology Bone Marrow Cells - metabolism Cell Differentiation Cells, Cultured Cryopreservation ELISA Enzyme-Linked Immunosorbent Assay Freezing Gene Expression Humans Macrophage colony-stimulating factor Macrophage Colony-Stimulating Factor - genetics Macrophage Colony-Stimulating Factor - metabolism Microarray analysis Osteoclast Osteoclasts - cytology Osteoclasts - metabolism Periodontal Ligament - cytology Periodontal Ligament - metabolism Periodontal ligament cells Quantitative real-time polymerase chain reaction RANK Ligand - metabolism Real-Time Polymerase Chain Reaction Root resorption Up-Regulation Western blotting |
| Title | Cryopreservation induces macrophage colony stimulating factor from human periodontal ligament cells in vitro |
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