Expression of vitamin D 1α-hydroxylase in human gingival fibroblasts in vivo
Vitamin D 1α-hydroxylase CYP27B1 is the key factor in the vitamin D pathway. Previously, we analyzed the expression of CYP27B1 in human gingival fibroblasts in vitro. In the present study, we analyzed the gingival expression of CYP27B1 in vivo. Forty-two patients with periodontitis Stage IV Grade C...
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Published in | PeerJ (San Francisco, CA) Vol. 9; p. e10279 |
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Format | Journal Article |
Language | English |
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04.01.2021
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ISSN | 2167-8359 2167-8359 |
DOI | 10.7717/peerj.10279 |
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Abstract | Vitamin D 1α-hydroxylase CYP27B1 is the key factor in the vitamin D pathway. Previously, we analyzed the expression of CYP27B1 in human gingival fibroblasts in vitro. In the present study, we analyzed the gingival expression of CYP27B1 in vivo.
Forty-two patients with periodontitis Stage IV Grade C and 33 controls were recruited. All patients with periodontitis had unsalvageable teeth and part of the wall of the periodontal pocket was resected and obtained after tooth extraction. All controls needed crown-lengthening surgery, and samples of gingiva resected during surgery were also harvested. All the individuals' gingivae were used for immunohistochemistry and immunofluorescence. In addition, gingivae from seventeen subjects of the diseased group and twelve subjects of the control group were analyzed by real-time PCR.
Expression of CYP27B1 was detected both in gingival epithelia and in gingival connective tissues, and the expression in connective tissues colocalized with vimentin, indicating that CYP27B1 protein is expressed in gingival fibroblasts. The expression of CYP27B1 mRNA in gingival connective tissues and the CYP27B1 staining scores in gingival fibroblasts in the diseased group were significantly higher than those in the control group.
Expression of CYP27B1 in human gingival tissues was detected, not only in the fibroblasts of gingival connective tissues, but also in the gingival epithelial cells, and might be positively correlated with periodontal inflammation. |
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AbstractList | Background Vitamin D 1α-hydroxylase CYP27B1 is the key factor in the vitamin D pathway. Previously, we analyzed the expression of CYP27B1 in human gingival fibroblasts in vitro. In the present study, we analyzed the gingival expression of CYP27B1 in vivo. Methods Forty-two patients with periodontitis Stage IV Grade C and 33 controls were recruited. All patients with periodontitis had unsalvageable teeth and part of the wall of the periodontal pocket was resected and obtained after tooth extraction. All controls needed crown-lengthening surgery, and samples of gingiva resected during surgery were also harvested. All the individuals’ gingivae were used for immunohistochemistry and immunofluorescence. In addition, gingivae from seventeen subjects of the diseased group and twelve subjects of the control group were analyzed by real-time PCR. Results Expression of CYP27B1 was detected both in gingival epithelia and in gingival connective tissues, and the expression in connective tissues colocalized with vimentin, indicating that CYP27B1 protein is expressed in gingival fibroblasts. The expression of CYP27B1 mRNA in gingival connective tissues and the CYP27B1 staining scores in gingival fibroblasts in the diseased group were significantly higher than those in the control group. Conclusions Expression of CYP27B1 in human gingival tissues was detected, not only in the fibroblasts of gingival connective tissues, but also in the gingival epithelial cells, and might be positively correlated with periodontal inflammation. Vitamin D 1α-hydroxylase CYP27B1 is the key factor in the vitamin D pathway. Previously, we analyzed the expression of CYP27B1 in human gingival fibroblasts in vitro. In the present study, we analyzed the gingival expression of CYP27B1 in vivo. Forty-two patients with periodontitis Stage IV Grade C and 33 controls were recruited. All patients with periodontitis had unsalvageable teeth and part of the wall of the periodontal pocket was resected and obtained after tooth extraction. All controls needed crown-lengthening surgery, and samples of gingiva resected during surgery were also harvested. All the individuals' gingivae were used for immunohistochemistry and immunofluorescence. In addition, gingivae from seventeen subjects of the diseased group and twelve subjects of the control group were analyzed by real-time PCR. Expression of CYP27B1 was detected both in gingival epithelia and in gingival connective tissues, and the expression in connective tissues colocalized with vimentin, indicating that CYP27B1 protein is expressed in gingival fibroblasts. The expression of CYP27B1 mRNA in gingival connective tissues and the CYP27B1 staining scores in gingival fibroblasts in the diseased group were significantly higher than those in the control group. Expression of CYP27B1 in human gingival tissues was detected, not only in the fibroblasts of gingival connective tissues, but also in the gingival epithelial cells, and might be positively correlated with periodontal inflammation. Vitamin D 1α-hydroxylase CYP27B1 is the key factor in the vitamin D pathway. Previously, we analyzed the expression of CYP27B1 in human gingival fibroblasts in vitro. In the present study, we analyzed the gingival expression of CYP27B1 in vivo.BACKGROUNDVitamin D 1α-hydroxylase CYP27B1 is the key factor in the vitamin D pathway. Previously, we analyzed the expression of CYP27B1 in human gingival fibroblasts in vitro. In the present study, we analyzed the gingival expression of CYP27B1 in vivo.Forty-two patients with periodontitis Stage IV Grade C and 33 controls were recruited. All patients with periodontitis had unsalvageable teeth and part of the wall of the periodontal pocket was resected and obtained after tooth extraction. All controls needed crown-lengthening surgery, and samples of gingiva resected during surgery were also harvested. All the individuals' gingivae were used for immunohistochemistry and immunofluorescence. In addition, gingivae from seventeen subjects of the diseased group and twelve subjects of the control group were analyzed by real-time PCR.METHODSForty-two patients with periodontitis Stage IV Grade C and 33 controls were recruited. All patients with periodontitis had unsalvageable teeth and part of the wall of the periodontal pocket was resected and obtained after tooth extraction. All controls needed crown-lengthening surgery, and samples of gingiva resected during surgery were also harvested. All the individuals' gingivae were used for immunohistochemistry and immunofluorescence. In addition, gingivae from seventeen subjects of the diseased group and twelve subjects of the control group were analyzed by real-time PCR.Expression of CYP27B1 was detected both in gingival epithelia and in gingival connective tissues, and the expression in connective tissues colocalized with vimentin, indicating that CYP27B1 protein is expressed in gingival fibroblasts. The expression of CYP27B1 mRNA in gingival connective tissues and the CYP27B1 staining scores in gingival fibroblasts in the diseased group were significantly higher than those in the control group.RESULTSExpression of CYP27B1 was detected both in gingival epithelia and in gingival connective tissues, and the expression in connective tissues colocalized with vimentin, indicating that CYP27B1 protein is expressed in gingival fibroblasts. The expression of CYP27B1 mRNA in gingival connective tissues and the CYP27B1 staining scores in gingival fibroblasts in the diseased group were significantly higher than those in the control group.Expression of CYP27B1 in human gingival tissues was detected, not only in the fibroblasts of gingival connective tissues, but also in the gingival epithelial cells, and might be positively correlated with periodontal inflammation.CONCLUSIONSExpression of CYP27B1 in human gingival tissues was detected, not only in the fibroblasts of gingival connective tissues, but also in the gingival epithelial cells, and might be positively correlated with periodontal inflammation. |
ArticleNumber | e10279 |
Author | Su, Jing Liu, Kaining Hou, Jianxia Meng, Huanxin Zhang, Jianyun Han, Bing |
Author_xml | – sequence: 1 givenname: Kaining surname: Liu fullname: Liu, Kaining organization: Department of Periodontology, Peking University School and Hospital of Stomatology, Beijing, China, National Clinical Research Center for Oral Diseases, Beijing, China, National Engineering Laboratory for Digital and Material Technology of Stomatology, Beijing, China, Beijing Key Laboratory of Digital Stomatology, Beijing, China – sequence: 2 givenname: Bing surname: Han fullname: Han, Bing organization: National Clinical Research Center for Oral Diseases, Beijing, China, National Engineering Laboratory for Digital and Material Technology of Stomatology, Beijing, China, Beijing Key Laboratory of Digital Stomatology, Beijing, China, Department of Cariology and Endodontology, Peking University School and Hospital of Stomatology, Beijing, China – sequence: 3 givenname: Jianxia surname: Hou fullname: Hou, Jianxia organization: Department of Periodontology, Peking University School and Hospital of Stomatology, Beijing, China, National Clinical Research Center for Oral Diseases, Beijing, China, National Engineering Laboratory for Digital and Material Technology of Stomatology, Beijing, China, Beijing Key Laboratory of Digital Stomatology, Beijing, China – sequence: 4 givenname: Jianyun surname: Zhang fullname: Zhang, Jianyun organization: National Clinical Research Center for Oral Diseases, Beijing, China, National Engineering Laboratory for Digital and Material Technology of Stomatology, Beijing, China, Beijing Key Laboratory of Digital Stomatology, Beijing, China, Department of Oral Pathology, Peking University School and Hospital of Stomatology, Beijing, China – sequence: 5 givenname: Jing surname: Su fullname: Su, Jing organization: Department of Pathology, Peking University Health Science Center, Beijing, China – sequence: 6 givenname: Huanxin surname: Meng fullname: Meng, Huanxin organization: Department of Periodontology, Peking University School and Hospital of Stomatology, Beijing, China, National Clinical Research Center for Oral Diseases, Beijing, China, National Engineering Laboratory for Digital and Material Technology of Stomatology, Beijing, China, Beijing Key Laboratory of Digital Stomatology, Beijing, China |
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Keywords | 25-hydroxyvitamin D3 1-alpha-hydroxylase Periodontitis Gene expression Gingiva |
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Snippet | Vitamin D 1α-hydroxylase CYP27B1 is the key factor in the vitamin D pathway. Previously, we analyzed the expression of CYP27B1 in human gingival fibroblasts in... Background Vitamin D 1α-hydroxylase CYP27B1 is the key factor in the vitamin D pathway. Previously, we analyzed the expression of CYP27B1 in human gingival... |
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SubjectTerms | Antigens Biotechnology Cell Biology Connective tissues Dentistry Epithelial cells Fibroblasts Gene expression Gingiva Histology Hydroxylase Immunofluorescence Immunohistochemistry Infectious Diseases Inflammation Molecular Biology Monoclonal antibodies mRNA Periodontitis Surgery Teeth Vimentin Vitamin D |
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Title | Expression of vitamin D 1α-hydroxylase in human gingival fibroblasts in vivo |
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