Temporal gene expression profiling during early-stage traumatic temporomandibular joint bony ankylosis in a sheep model

被引:1
作者
Zhang, Tong-Mei [1 ,2 ,3 ,4 ]
Yang, Kun [5 ]
Jiao, Mai-Ning [6 ]
Zhao, Yan [4 ]
Xu, Zhao-Yuan [7 ,8 ]
Zhang, Guan-Meng [7 ,8 ]
Wang, Hua-Lun [9 ]
Liang, Su-Xia [8 ,10 ]
Yan, Ying-Bin [7 ,8 ]
机构
[1] Tianjin Med Univ, Natl Clin Res Ctr Canc, Canc Inst & Hosp, West Huan Hu Rd, Tianjin 30060, Peoples R China
[2] Tianjins Clin Res Ctr Canc, West Huan Hu Rd, Tianjin 30060, Peoples R China
[3] Key Lab Canc Prevent & Therapy, West Huan Hu Rd, Tianjin 30060, Peoples R China
[4] Tianjin Med Univ, 22 Qi Xiangtai Rd, Tianjin 300070, Peoples R China
[5] China Three Gorges Univ, Affiliated Renhe Hosp, Dept Oromaxillofacial Head & Neck Surg, 410 Yiling Ave, Yichang 443001, Hubei, Peoples R China
[6] Weifang peoples Hosp, Dept Oral & Maxillofacial Surg, 151 GuangWen St, Weifang 261000, Shandong, Peoples R China
[7] Nankai Univ, Tianjin Stomatol Hosp, Sch Med, Dept Oromaxillofacial Head & Neck Surg, 75 Dagu Rd, Tianjin 300041, Peoples R China
[8] Tianjin Key Lab Oral & Maxillofacial Funct Reconst, 75 Dagu Rd, Tianjin 300041, Peoples R China
[9] Jining Stomatol Hosp, Dept Oral & Maxillofacial Surg, 22 Communist Youth League Rd, Jining 272000, Shandong, Peoples R China
[10] Nankai Univ, Tianjin Stomatol Hosp, Sch Med, Dept Operat Dent & Endodont, 75 Dagu Rd, Tianjin 300041, Peoples R China
关键词
Temporomandibular joint; Mandibular condyle; Ankylosis; Microarray analysis; Trauma; Sheep; Animal; MESENCHYMAL STEM-CELLS; MOLECULAR PATHOPHYSIOLOGY; PILOT TRIAL; DIFFERENTIATION; PROTOCOL;
D O I
10.1186/s12903-024-03971-x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
BackgroundInvestigating the molecular biology underpinning the early-stage of traumatic temporomandibular joint (TMJ) ankylosis is crucial for discovering new ways to prevent the disease. This study aimed to explore the dynamic changes of transcriptome from the intra-articular hematoma or the newly generated ankylosed callus during the onset and early progression of TMJ ankylosis.MethodsBased on a well-established sheep model of TMJ bony ankylosis, the genome-wide microarray data were obtained from samples at postoperative Days 1, 4, 7, 9, 11, 14 and 28, with intra-articular hematoma at Day 1 serving as controls. Fold changes in gene expression values were measured, and genes were identified via clustering based on time series analysis and further categorised into three major temporal classes: increased, variable and decreased expression groups. The genes in these three temporal groups were further analysed to reveal pathways and establish their biological significance.ResultsOsteoblastic and angiogenetic genes were found to be significantly expressed in the increased expression group. Genes linked to inflammation and osteoclasts were found in the decreased expression group. The various biological processes and pathways related to each temporal expression group were identified, and the increased expression group comprised genes exclusively involved in the following pathways: Hippo signaling pathway, Wnt signaling pathway and Rap 1 signaling pathway. The decreased expression group comprised genes exclusively involved in immune-related pathways and osteoclast differentiation. The variable expression group consisted of genes associated with DNA replication, DNA repair and DNA recombination. Significant biological pathways and transcription factors expressed at each time point postoperatively were also identified.ConclusionsThese data, for the first time, presented the temporal gene expression profiling and reveal the important process of molecular biology in the early-stage of traumatic TMJ bony ankylosis. The findings might contributed to identifying potential targets for the treatment of TMJ ankylosis.
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页数:19
相关论文
共 49 条
[1]   Molecular mechanisms controlling bone formation during fracture healing and distraction osteogenesis [J].
Ai-Aql, Z. S. ;
Alagl, A. S. ;
Graves, D. T. ;
Gerstenfeld, L. C. ;
Einhorn, T. A. .
JOURNAL OF DENTAL RESEARCH, 2008, 87 (02) :107-118
[2]   A LATS biosensor screen identifies VEGFR as a regulator of the Hippo pathway in angiogenesis [J].
Azad, T. ;
van Rensburg, H. J. Janse ;
Lightbody, E. D. ;
Neveu, B. ;
Champagne, A. ;
Ghaffari, A. ;
Kay, V. R. ;
Hao, Y. ;
Shen, H. ;
Yeung, B. ;
Croy, B. A. ;
Guan, K. L. ;
Pouliot, F. ;
Zhang, J. ;
Nicol, C. J. B. ;
Yang, X. .
NATURE COMMUNICATIONS, 2018, 9
[3]   Cellular biology of fracture healing [J].
Bahney, Chelsea S. ;
Zondervan, Robert L. ;
Allison, Patrick ;
Theologis, Alekos ;
Ashley, Jason W. ;
Ahn, Jaimo ;
Miclau, Theodore ;
Marcucio, Ralph S. ;
Hankenson, Kurt D. .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2019, 37 (01) :35-50
[4]   Transcriptional Analysis of Fracture Healing and the Induction of Embryonic Stem Cell-Related Genes [J].
Bais, Manish ;
McLean, Jody ;
Sebastiani, Paola ;
Young, Megan ;
Wigner, Nathan ;
Smith, Temple ;
Kotton, Darrell N. ;
Einhorn, Thomas A. ;
Gerstenfeld, Louis C. .
PLOS ONE, 2009, 4 (05)
[5]   The role of Toll-like receptors in the host response to viruses [J].
Bowie, AG ;
Haga, IR .
MOLECULAR IMMUNOLOGY, 2005, 42 (08) :859-867
[6]   Gasdermin D in pyroptosis [J].
Burdette, Brandon E. ;
Esparza, Ashley N. ;
Zhu, Hua ;
Wang, Shanzhi .
ACTA PHARMACEUTICA SINICA B, 2021, 11 (09) :2768-2782
[7]  
Byrd-Leifer CA, 2001, EUR J IMMUNOL, V31, P2448, DOI 10.1002/1521-4141(200108)31:8<2448::AID-IMMU2448>3.0.CO
[8]  
2-N
[9]   Wnt Pathway, an Essential Role in Bone Regeneration [J].
Chen, Yan ;
Alman, Benjamin A. .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2009, 106 (03) :353-362
[10]   Differential temporal expression of members of the transforming growth factor β superfamily during murine fracture healing [J].
Cho, TJ ;
Gerstenfeld, LC ;
Einhorn, TA .
JOURNAL OF BONE AND MINERAL RESEARCH, 2002, 17 (03) :513-520