The role of lateral pterygoid muscle in the traumatic temporomandibular joint ankylosis: A gene chip based analysis

Zhang,Jianying; Sun,Xiangzhao; Jia,Sen; Jiang,Xin; Deng,Tiange; Liu,Ping; Hu,Kaijin

doi:10.3892/mmr.2019.10078

The role of lateral pterygoid muscle in the traumatic temporomandibular joint ankylosis: A gene chip based analysis

Authors:
- Jianying Zhang
- Xiangzhao Sun
- Sen Jia
- Xin Jiang
- Tiange Deng
- Ping Liu
- Kaijin Hu
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Affiliations: State Key Laboratory of Military Stomatology, National Clinical Research Center for Oral Diseases and Shaanxi Clinical Research Center for Oral Diseases, Department of Oral Surgery, School of Stomatology, The Fourth Military Medical University, Xi'an, Shaanxi 710032, P.R. China
Published online on: March 22, 2019 https://doi.org/10.3892/mmr.2019.10078
Pages: 4297-4305
Copyright: © Zhang et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

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Abstract

Traumatic temporomandibular joint ankylosis (TMJA) is a common disease and disorder of the temporomandibular joint (TMJ); however, its pathogenesis has yet to be completely elucidated. In the authors' previous studies, the lateral pterygoid muscle (LPM) was confirmed to exert a function in distraction osteogenesis (DO) during the healing of a condylar fracture, which resulted in the formation of excess bone. The aim of the present study was to investigate alterations in the expression of any associated genes via an Affymetrix GeneChip method. The traumatic TMJA model was fabricated by a condylar fracture in the TMJ area of sheep with either a dissected LPM (LPD) or normal (LPN). The untreated sheep served as a control. At 4‑ and 12 weeks post‑surgery, the condylar zone was isolated to perform the gene chip analysis, which was performed according to a standard Affymetrix protocol. The validated genes were further evaluated by reverse transcription‑quantitative polymerase chain reaction (RT‑qPCR). The gene chip analysis indicated that the LPN gene expression pattern was similar compared with the DO process, while LPD was similar to that of normal bone fracture healing. The validated genes were collagen type II α1 chain, C‑type lectin domain family 3 member A, interleukin 1A, cartilage oligomeric matrix protein, chondromodulin (LECT1), calcitonin receptor (CALCR), transforming growth factor (TGF)‑β1, Fos proto‑oncogene (FOS), bone γ‑carboxyglutamate protein and bone morphogenic protein (BMP)7, among which, BMP7, LECT1, CALCR and FOS were confirmed by RT‑qPCR. In conclusion, the present study demonstrated that LPM exerts a DO effect during the pathogenesis of traumatic TMJA, which may provide a novel target for preventing TMJA.

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