Expressions of parathyroid hormone-related protein (PTHrP) and parathyroid hormone receptor-1 (PTH1R) in the condylar cartilage of temporomandibular joint modulated by occlusal elevation

被引:1
作者
Zhuang, Qianzhi [1 ,2 ]
Li, Bing [1 ]
Wu, Xiuping [1 ]
机构
[1] Shanxi Med Univ, Sch & Hosp Stomatol, Shanxi Prov Key Lab Oral Dis Prevent & New Mat, 63 Xinjian Nan Rd, Taiyuan 030000, Shanxi, Peoples R China
[2] Weifang Hosp Tradit Chinese Med, Dept Stomatol, Weifang, Shandong, Peoples R China
关键词
PTHrP; PTH1R; Temporomandibular joint osteoarthritis; Condylar cartilage; Occlusal elevation; CHONDROCYTE DIFFERENTIATION; TERMINAL DIFFERENTIATION; ARTICULAR CHONDROCYTES; OSTEOARTHRITIS; INVOLVEMENT; PROGRESSION; SHEEP;
D O I
10.1016/j.jds.2022.08.001
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background/purpose: Parathyroid hormone-related protein (PTHrP) is an important regulatory factor in the growth, development and remodeling of bone or cartilage, and acts through its sole receptor, parathyroid hormone receptor-1 (PTH1R). The present study aimed to research the expression changes of PTHrP, PTH1R and other relevant factors in condylar cartilage during the progress of temporomandibular joint osteoarthritis (TMJOA).Materials and methods: The animal model of TMJOA was constructed by the "resin-modified method", and Sprague Dawley (SD) rats were euthanized at 2 weeks, 4 weeks, 6 weeks and 8 weeks after occlusal elevation. The histological changes of condylar cartilage were observed by X-ray, hematoxylin-eosin (HE) and safranine O-fast green (SO-FG) staining. The expressions of PTHrP, PTH1R, Ki67, Collagen II (Col II), Collagen X (Col X) and Caspase 3 in each group were detected by quantitative real-time polymerase chain reaction (qRT-PCR) and immunohisto-chemistry (IHC).Results: TMJOA progression was time-dependent. In the experimental group, PTHrP expression was unimodal with a peak at 4 weeks, but PTH1R expression showed a decreasing trend. From 2 weeks to 8 weeks in the experimental group, Col X expression rather than Caspase 3 expression was negatively related to PTHrP's, which has no positive relation to Ki67 or Col II. These results demonstrated abnormal occlusal load may be an important pathogenic factor of TMJOA.Conclusion: It may be one of the reasons of TMJOA progression that PTHrP can't play an effec-tive role due to the low expression of PTH1R. PTHrP may be a direct factor regulating the hy-pertrophic differentiation of chondrocytes, but it does not directly regulate the proliferation and apoptosis of chondrocytes, and the realization of both regulatory effects may depend on the inhibition of hypertrophic differentiation. 2022 Association for Dental Sciences of the Republic of China. Publishing services by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons. org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:626 / 635
页数:10
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