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转化生长因子-β与乳牙生理性牙根吸收

TGF-β and Physiological Root Resorption of Deciduous Teeth.

作者信息

Shimazaki Emi, Karakida Takeo, Yamamoto Ryuji, Kobayashi Saeko, Fukae Makoto, Yamakoshi Yasuo, Asada Yoshinobu

机构信息

Department of Pediatric Dentistry, School of Dental Medicine, Tsurumi University, 2-1-3 Tsurumi, Tsurumi-ku, Yokohama 230-8501, Japan.

Department of Biochemistry and Molecular Biology, School of Dental Medicine, Tsurumi University, 2-1-3 Tsurumi, Tsurumi-ku, Yokohama 230-8501, Japan.

出版信息

Int J Mol Sci. 2016 Dec 27;18(1):49. doi: 10.3390/ijms18010049.

Abstract

The present study was performed to examine how transforming growth factor β (TGF-β) in root-surrounding tissues on deciduous teeth regulates the differentiation induction into odontoclasts during physiological root resorption. We prepared root-surrounding tissues with (R) or without (N) physiological root resorption scraped off at three regions (R1-R3 or N1-N3) from the cervical area to the apical area of the tooth and measured both TGF-β and the tartrate-resistant acid phosphatase (TRAP) activities. The TGF-β activity level was increased in N1-N3, whereas the TRAP activity was increased in R2 and R3. In vitro experiments for the receptor activator of nuclear factor-κB (NF-κB) ligand (RANKL)-mediated osteoclast differentiation revealed that proteins from N1-N3 and R1-R3 enhanced the TRAP activity in RAW264 cells. A genetic study indicated that the mRNA levels of TGF-β1 in N1 and N2 were significantly increased, and corresponded with levels of osteoprotegerin (OPG). In contrast, the expression level of RANKL was increased in R2 and R3. Our findings suggest that TGF-β is closely related to the regulation of OPG induction and RANKL-mediated odontoclast differentiation depending on the timing of RANKL and OPG mRNA expression in the root-surrounding tissues of deciduous teeth during physiological root resorption.

摘要

本研究旨在探讨乳牙牙根周围组织中的转化生长因子β(TGF-β)在生理性牙根吸收过程中如何调节破牙细胞的分化诱导。我们从牙齿颈部到根尖区域的三个部位(R1-R3或N1-N3)刮取有(R)或无(N)生理性牙根吸收的牙根周围组织,并测量TGF-β和抗酒石酸酸性磷酸酶(TRAP)的活性。N1-N3中的TGF-β活性水平升高,而R2和R3中的TRAP活性升高。针对核因子κB(NF-κB)配体(RANKL)介导的破骨细胞分化的体外实验表明,来自N1-N3和R1-R3的蛋白质增强了RAW264细胞中的TRAP活性。一项基因研究表明,N1和N2中TGF-β1的mRNA水平显著升高,且与骨保护素(OPG)水平相对应。相反,RANKL的表达水平在R2和R3中升高。我们的研究结果表明,在生理性牙根吸收过程中,根据乳牙牙根周围组织中RANKL和OPG mRNA表达的时间,TGF-β与OPG诱导的调节以及RANKL介导的破牙细胞分化密切相关。

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