{"title":"The Anti-Inflammatory Effect of 6% HES 200/0.5 on RAW264.7 Cells Induced by LPS through HMGB1/NF-κB Signaling Pathway","authors":"J Zhang, Yongli Wang, Jianzhong Zhang, Shaoyan Huang","doi":"10.2485/jhtb.31.245","DOIUrl":"https://doi.org/10.2485/jhtb.31.245","url":null,"abstract":"","PeriodicalId":16040,"journal":{"name":"Journal of Hard Tissue Biology","volume":"1 1","pages":""},"PeriodicalIF":0.4,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"68966418","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Huai-chun Chang, Tingting Jiang, Liang Kou, Duo Li, Xinchen Yu, Youqin Li, Lei Zhang
: We aimed to evaluate the regulatory effects of miR-148a-3p on stem cell osteogenic differentiation and enamel development by targeting runt-related transcription factor 2 (RUNX2) and E-cadherin, respectively. TargetScan software was utilized to predict the binding sites between miR-148a-3p and osteogenic marker gene RUNX2 or E-cadherin. The changes in miR-148a-3p expression during osteogenic differentiation of epidermal stem cells were detected. After transfec tion with miR-148a-3p mimics or miR-148a-3p inhibitor, epidermal stem cells were induced towards osteogenic differentia tion, and the changes in RUNX2 expression were measured. The changes in miR-148a-3p expression during enamel devel opment regulated by epidermal stem cells were determined. After liposome-mediated transfection with miR-148a-3p mimics or miR-148a-3p inhibitor, epidermal stem cells were induced towards ameloblast development. Cell proliferation and apoptosis abilities were tested using methyl thiazolyl tetrazolium assay and flow cytometry, respectively. The expres sion of miR-148a-3p was detected by RT-PCR. The protein expressions of Wnt1, β-catenin, RUNX2 and E-cadherin were measured by Western blotting. Epidermal stem cells differentiated into osteoblasts through osteogenic induction culture. On 5, 12, 15 and 30 d, epidermal stem cells gradually differentiated into osteoblasts through epithelial aggregation and depres sion, mesenchymal aggregation, and dentin and enamel secretion. After transfection, compared with negative control (NC) group, the cell viability of miR-148-3p group significantly decreased (P<0.05), and the apoptosis rate increased (P<0.01). The viability of miR-148-3p inhibitor group significantly increased (P<0.05), while the apoptosis rate reduced (P<0.01). The dual-luciferase reporter assay showed that miR-148a-3p targeted Wnt1. Compared with NC group, the expression of miR-148a-3p significantly rose in miR-148a-3p group (P<0.001), and the protein expression levels of Wnt1, β-catenin, RUNX2 and E-cadherin significantly decreased. Compared with NC group, the expression of miR-148a-3p in miR-148a-3p inhibitor group significantly decreased (P<0.05), and the protein expression levels of Wnt1, β-catenin, RUNX2 and E-cad herin significantly increased. MiR-148a-3p is highly expressed in and regulates osteogenic differentiation and enamel de velopment through targeting RUNX2 and E-cadherin respectively via the Wnt1/β-catenin pathway, which plays an impor tant role in cell differentiation, stem cell proliferation and enamel development.
{"title":"MiR-148a-3p Regulates Stem Cell Osteogenic Differentiation and Enamel Development by Targeting Runt-Related Transcription Factor 2 and E-cadherin via the Wnt1/β-catenin Signaling Pathway","authors":"Huai-chun Chang, Tingting Jiang, Liang Kou, Duo Li, Xinchen Yu, Youqin Li, Lei Zhang","doi":"10.2485/jhtb.31.141","DOIUrl":"https://doi.org/10.2485/jhtb.31.141","url":null,"abstract":": We aimed to evaluate the regulatory effects of miR-148a-3p on stem cell osteogenic differentiation and enamel development by targeting runt-related transcription factor 2 (RUNX2) and E-cadherin, respectively. TargetScan software was utilized to predict the binding sites between miR-148a-3p and osteogenic marker gene RUNX2 or E-cadherin. The changes in miR-148a-3p expression during osteogenic differentiation of epidermal stem cells were detected. After transfec tion with miR-148a-3p mimics or miR-148a-3p inhibitor, epidermal stem cells were induced towards osteogenic differentia tion, and the changes in RUNX2 expression were measured. The changes in miR-148a-3p expression during enamel devel opment regulated by epidermal stem cells were determined. After liposome-mediated transfection with miR-148a-3p mimics or miR-148a-3p inhibitor, epidermal stem cells were induced towards ameloblast development. Cell proliferation and apoptosis abilities were tested using methyl thiazolyl tetrazolium assay and flow cytometry, respectively. The expres sion of miR-148a-3p was detected by RT-PCR. The protein expressions of Wnt1, β-catenin, RUNX2 and E-cadherin were measured by Western blotting. Epidermal stem cells differentiated into osteoblasts through osteogenic induction culture. On 5, 12, 15 and 30 d, epidermal stem cells gradually differentiated into osteoblasts through epithelial aggregation and depres sion, mesenchymal aggregation, and dentin and enamel secretion. After transfection, compared with negative control (NC) group, the cell viability of miR-148-3p group significantly decreased (P<0.05), and the apoptosis rate increased (P<0.01). The viability of miR-148-3p inhibitor group significantly increased (P<0.05), while the apoptosis rate reduced (P<0.01). The dual-luciferase reporter assay showed that miR-148a-3p targeted Wnt1. Compared with NC group, the expression of miR-148a-3p significantly rose in miR-148a-3p group (P<0.001), and the protein expression levels of Wnt1, β-catenin, RUNX2 and E-cadherin significantly decreased. Compared with NC group, the expression of miR-148a-3p in miR-148a-3p inhibitor group significantly decreased (P<0.05), and the protein expression levels of Wnt1, β-catenin, RUNX2 and E-cad herin significantly increased. MiR-148a-3p is highly expressed in and regulates osteogenic differentiation and enamel de velopment through targeting RUNX2 and E-cadherin respectively via the Wnt1/β-catenin pathway, which plays an impor tant role in cell differentiation, stem cell proliferation and enamel development.","PeriodicalId":16040,"journal":{"name":"Journal of Hard Tissue Biology","volume":"1 1","pages":""},"PeriodicalIF":0.4,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"68966038","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
: Multiple experimental pieces of evidence have confirmed that fully understanding the regulatory mechanisms of osteogenic differentiation of periodontal ligament stem cells (PDLSCs) can better promote and improve the ability of perio dontal tissues to regenerate and alleviate periodontal diseases. This study aimed to reveal whether the long noncoding RNA (lncRNA) ZNF710-AS1 plays a role in the osteogenic differentiation of PDLSCs and its molecular mechanisms. Microarray datasets GSE159507 and GSE159508 were retrieved from the Gene Expression Omnibus database and differentially ex pressed genes were identified using R language (limma package). The results revealed that the expression of ZNF710-AS1 and bone morphogenetic protein 6 (BMP6) was upregulated whereas that of miR-146a-5p/miR-146b-5p was downregulated during the osteogenic differentiation of PDLSCs. PDLSCs were successfully isolated and cultured in vitro . Osteogenic and adipogenic differentiation abilities were evaluated by performing alizarin red staining and oil red O staining, respectively. Overexpression of ZNF710-AS1 significantly increased the osteogenic differentiation ability of PDLSCs by upregulating the expression of BMP6 and phosphorylation-SMAD family member 1/5/9 (p-Smad1/5/9) and competitively sponging miR-146a-5p/miR-146b-5p and acting as a competing endogenous RNA (ceRNA). This study demonstrated that ZNF710-AS1 promotes the osteogenic differentiation of PDLSCs by upregulating BMP6/Smad1/5/9 expression and acting as a ceR NA for miR-146a-5p and miR-146b-5p.
{"title":"lncRNA ZNF710-AS1 Acts as a ceRNA for miR-146a-5p and miR-146b-5p to Accelerate Osteogenic Differentiation of PDLSCs by Upregulating the BMP6/Smad1/5/9 Pathway","authors":"Ying Liu, D. Fu","doi":"10.2485/jhtb.31.231","DOIUrl":"https://doi.org/10.2485/jhtb.31.231","url":null,"abstract":": Multiple experimental pieces of evidence have confirmed that fully understanding the regulatory mechanisms of osteogenic differentiation of periodontal ligament stem cells (PDLSCs) can better promote and improve the ability of perio dontal tissues to regenerate and alleviate periodontal diseases. This study aimed to reveal whether the long noncoding RNA (lncRNA) ZNF710-AS1 plays a role in the osteogenic differentiation of PDLSCs and its molecular mechanisms. Microarray datasets GSE159507 and GSE159508 were retrieved from the Gene Expression Omnibus database and differentially ex pressed genes were identified using R language (limma package). The results revealed that the expression of ZNF710-AS1 and bone morphogenetic protein 6 (BMP6) was upregulated whereas that of miR-146a-5p/miR-146b-5p was downregulated during the osteogenic differentiation of PDLSCs. PDLSCs were successfully isolated and cultured in vitro . Osteogenic and adipogenic differentiation abilities were evaluated by performing alizarin red staining and oil red O staining, respectively. Overexpression of ZNF710-AS1 significantly increased the osteogenic differentiation ability of PDLSCs by upregulating the expression of BMP6 and phosphorylation-SMAD family member 1/5/9 (p-Smad1/5/9) and competitively sponging miR-146a-5p/miR-146b-5p and acting as a competing endogenous RNA (ceRNA). This study demonstrated that ZNF710-AS1 promotes the osteogenic differentiation of PDLSCs by upregulating BMP6/Smad1/5/9 expression and acting as a ceR NA for miR-146a-5p and miR-146b-5p.","PeriodicalId":16040,"journal":{"name":"Journal of Hard Tissue Biology","volume":"92 1","pages":""},"PeriodicalIF":0.4,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"68966411","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Seiko Tanzawa, Kei Kitamura, N. Ishikawa, Yoshiki Tamiya, R. Sako, M. Furusawa, Hitoshi Yamamoto
{"title":"Immunohistochemical Observation on the Distribution and Morphological Changes of GAP-43 Positive Structures in the Formation of Experimental Apical Periodontitis of Rat Molars","authors":"Seiko Tanzawa, Kei Kitamura, N. Ishikawa, Yoshiki Tamiya, R. Sako, M. Furusawa, Hitoshi Yamamoto","doi":"10.2485/jhtb.31.155","DOIUrl":"https://doi.org/10.2485/jhtb.31.155","url":null,"abstract":"","PeriodicalId":16040,"journal":{"name":"Journal of Hard Tissue Biology","volume":"1 1","pages":""},"PeriodicalIF":0.4,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"68966104","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
: Fracture healing is a complex dynamic process that involves the balance between osteoblasts and osteoclasts. Sev-eral microRNAs (miRNAs) have been shown to participate in fracture healing. In this study, we investigated the role of miR-324-3p in osteoblast differentiation. MC3T3-E1 cell differentiation was induced by icariin, and miR-324-3p expression levels during cell differentiation were measured using qRT-PCR. Cell proliferation and differentiation were assessed to eval uate the function of miR-324-3p. Luciferase activity was used for target gene verification. During MC3T3-E1 differentia tion, miR-324-3p levels gradually increased over time. Further experiments showed that miR-324-3p overexpression significantly promoted cell viability, whereas miR-324-3p downregulation showed the opposite effect. For cells with miR-324-3p mimic, the levels of bone sialoprotein, Runx2, osteocalcin, and alkaline phosphatase activity were significantly elevated. SMAD7 is the target gene of miR-324-3p, and its level is gradually downregulated during MC3T3-E1 cell differentiation. MiR-324-3p may promote MC3T3-E1 cell differentiation by targeting SMAD7.
{"title":"microRNA-324-3p Promotes Osteoblasts Differentiation via Suppressing SMAD7","authors":"Wei Xu, Rui Xia, Feng Tian, Lei Liu, Mengmeng Li, Shi-yuan Fang","doi":"10.2485/jhtb.31.263","DOIUrl":"https://doi.org/10.2485/jhtb.31.263","url":null,"abstract":": Fracture healing is a complex dynamic process that involves the balance between osteoblasts and osteoclasts. Sev-eral microRNAs (miRNAs) have been shown to participate in fracture healing. In this study, we investigated the role of miR-324-3p in osteoblast differentiation. MC3T3-E1 cell differentiation was induced by icariin, and miR-324-3p expression levels during cell differentiation were measured using qRT-PCR. Cell proliferation and differentiation were assessed to eval uate the function of miR-324-3p. Luciferase activity was used for target gene verification. During MC3T3-E1 differentia tion, miR-324-3p levels gradually increased over time. Further experiments showed that miR-324-3p overexpression significantly promoted cell viability, whereas miR-324-3p downregulation showed the opposite effect. For cells with miR-324-3p mimic, the levels of bone sialoprotein, Runx2, osteocalcin, and alkaline phosphatase activity were significantly elevated. SMAD7 is the target gene of miR-324-3p, and its level is gradually downregulated during MC3T3-E1 cell differentiation. MiR-324-3p may promote MC3T3-E1 cell differentiation by targeting SMAD7.","PeriodicalId":16040,"journal":{"name":"Journal of Hard Tissue Biology","volume":"1 1","pages":""},"PeriodicalIF":0.4,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"68966457","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Effects of TGF-β on Growth and Invasion of Human Oral Squamous Cell Carcinoma Cell Lines","authors":"Hitoe Ishiguro-Katsuta, Y. Okada","doi":"10.2485/jhtb.31.171","DOIUrl":"https://doi.org/10.2485/jhtb.31.171","url":null,"abstract":"","PeriodicalId":16040,"journal":{"name":"Journal of Hard Tissue Biology","volume":"1 1","pages":""},"PeriodicalIF":0.4,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"68966170","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Tomoki Hirano, T. Miura, Yuto Otsu, Atsuro Harada, Y. Asami, Noriko Iijima, Yukari Oda, Yoshitaka Furuya, Taichi Ito, Hodaka Sasaki, H. Sekine
: Surface modifications of implants can improve the rate of osseointegration. The aim of this study was to deter mine the effect of super-hydrophilic modification on tetragonal zirconia polycrystals (TZP) implant surface and its subse quent effect on the rate of osseointegration. The TZP implants were rendered super-hydrophilic by the use of ultraviolet light (UV) or via atmospheric-pressure plasma treatments (PL), on their surface and were compared to control specimen that any surface modification wasn’t performed (NC). According to the surface wettability and x-ray photoelectron spec troscopy (XPS) analysis, the contact angle of water droplets on the surface of UV and PL was 0 degree, and their C1s peak was less than that of NC. The push-in test and histological analysis revealed that the super-hydrophilic modification en hanced the bone-implant integration and the formation of new bone around the TZP implants. Additionally, carbon removal and surface wettability enhancement likely improved the osseointegration rate. The study, therefore, demonstrates the de-sign of future TZP implants, particularly for dental applications. This study explored the effect of super-hydrophilic surface modifica tion on TZP implants and its subsequent effect on the rate of osseointe gration in rats. In this study, UV and PL were used. These treatments had no detrimental effect on the TZP implant surface and demonstrated sufficient capacity for carbon removal and super-hydrophilicity for TZP implants. UV and PL TZP implants demonstrated improved osseointe gration rate compared to NC. Super-hydrophilic surface treatments have been used to improve the osseointegration rate of titanium implants. Ultraviolet light exposure en hances protein adsorption, bone marrow cell adhesion, osteoblast differ -entiation, and osseointegration rate of titanium implants 12) . A previous study demonstrated that 4-week-aged, Ultraviolet light treated titanium surfaces increased bioactivity to a level comparable to or greater than that of freshly prepared surfaces, owing to the restoration of super-hy-drophilicity 13) . Plasma-treated titanium surfaces promoted osteoblast proliferation 14) and increased bone-to-implant contact 15,16) . Ultraviolet light treatment enhanced osteoblast adhesion, proliferation, and mineralization in zirconia implants 22) and improved bone-to-implant contact and osseointegration 23) . Additionally, Plasma treatment enhanced the bio-compatibility of zirconia implants 24–26) . The findings of this study are consistent with those reported in the previous studies.
{"title":"The Effect of Super-Hydrophilic Treatment on Zirconia Implant Osseointegration in Rats","authors":"Tomoki Hirano, T. Miura, Yuto Otsu, Atsuro Harada, Y. Asami, Noriko Iijima, Yukari Oda, Yoshitaka Furuya, Taichi Ito, Hodaka Sasaki, H. Sekine","doi":"10.2485/jhtb.31.223","DOIUrl":"https://doi.org/10.2485/jhtb.31.223","url":null,"abstract":": Surface modifications of implants can improve the rate of osseointegration. The aim of this study was to deter mine the effect of super-hydrophilic modification on tetragonal zirconia polycrystals (TZP) implant surface and its subse quent effect on the rate of osseointegration. The TZP implants were rendered super-hydrophilic by the use of ultraviolet light (UV) or via atmospheric-pressure plasma treatments (PL), on their surface and were compared to control specimen that any surface modification wasn’t performed (NC). According to the surface wettability and x-ray photoelectron spec troscopy (XPS) analysis, the contact angle of water droplets on the surface of UV and PL was 0 degree, and their C1s peak was less than that of NC. The push-in test and histological analysis revealed that the super-hydrophilic modification en hanced the bone-implant integration and the formation of new bone around the TZP implants. Additionally, carbon removal and surface wettability enhancement likely improved the osseointegration rate. The study, therefore, demonstrates the de-sign of future TZP implants, particularly for dental applications. This study explored the effect of super-hydrophilic surface modifica tion on TZP implants and its subsequent effect on the rate of osseointe gration in rats. In this study, UV and PL were used. These treatments had no detrimental effect on the TZP implant surface and demonstrated sufficient capacity for carbon removal and super-hydrophilicity for TZP implants. UV and PL TZP implants demonstrated improved osseointe gration rate compared to NC. Super-hydrophilic surface treatments have been used to improve the osseointegration rate of titanium implants. Ultraviolet light exposure en hances protein adsorption, bone marrow cell adhesion, osteoblast differ -entiation, and osseointegration rate of titanium implants 12) . A previous study demonstrated that 4-week-aged, Ultraviolet light treated titanium surfaces increased bioactivity to a level comparable to or greater than that of freshly prepared surfaces, owing to the restoration of super-hy-drophilicity 13) . Plasma-treated titanium surfaces promoted osteoblast proliferation 14) and increased bone-to-implant contact 15,16) . Ultraviolet light treatment enhanced osteoblast adhesion, proliferation, and mineralization in zirconia implants 22) and improved bone-to-implant contact and osseointegration 23) . Additionally, Plasma treatment enhanced the bio-compatibility of zirconia implants 24–26) . The findings of this study are consistent with those reported in the previous studies.","PeriodicalId":16040,"journal":{"name":"Journal of Hard Tissue Biology","volume":"1 1","pages":""},"PeriodicalIF":0.4,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"68966357","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Calcitonin Gene-related Peptide Inhibits Osteoclast Differentiation by Inducing the Negative Regulators MafB and Bcl6","authors":"Kyoko Ishizuka","doi":"10.2485/jhtb.31.87","DOIUrl":"https://doi.org/10.2485/jhtb.31.87","url":null,"abstract":"","PeriodicalId":16040,"journal":{"name":"Journal of Hard Tissue Biology","volume":"1 1","pages":""},"PeriodicalIF":0.4,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"68966524","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Highly Expressed SPC25 Promotes the Stemness, Proliferation and EMT of Oral Squamous Cell Carcinoma Cells via Modulating the TGF-β Signaling Pathway","authors":"Qiufang Zhang, Zijun Zeng, Wen Xie, Zhimei Zeng","doi":"10.2485/jhtb.31.195","DOIUrl":"https://doi.org/10.2485/jhtb.31.195","url":null,"abstract":"","PeriodicalId":16040,"journal":{"name":"Journal of Hard Tissue Biology","volume":"1 1","pages":""},"PeriodicalIF":0.4,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"68966708","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Proviral Insertion in Murine Lymphomas 2 Promotes Inflammation and Inhibits Osteogenic Differentiation of Periodontal Ligament Cells via Regulating AMPK and NF-κB Signalings","authors":"Fan Ye, Hui Xu","doi":"10.2485/jhtb.31.215","DOIUrl":"https://doi.org/10.2485/jhtb.31.215","url":null,"abstract":"","PeriodicalId":16040,"journal":{"name":"Journal of Hard Tissue Biology","volume":"1 1","pages":""},"PeriodicalIF":0.4,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"68966336","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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