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破牙细胞中MT1-MMP在乳牙吸收过程中的表达。

Expression of MT1-MMP during deciduous tooth resorption in odontoclasts.

作者信息

Linsuwanont-Santiwong Busayarat, Takagi Yuzo, Ohya Keiichi, Shimokawa Hitoyata

机构信息

Department of Pediatric Dentistry, Faculty of Dentistry, Chulalongkorn University, Bangkok, Thailand.

出版信息

J Bone Miner Metab. 2006;24(6):447-53. doi: 10.1007/s00774-006-0714-z.

Abstract

Membrane type 1-matrix metalloproteinase (MT1-MMP) is a membrane-bound matrix metalloproteinase capable of mediating pericellular proteolysis of extracellular matrix components. In osteoclasts, the localization of MT1-MMP has been reported at the tips of specialized membrane protrusions (podosomes and lamellipodia) so that osteoclasts might use MT1-MMP to perform focal proteolysis and move through the extracellular matrix to the bone surface. The objectives of this study were to investigate an association of MT1-MMP in physiological root resorption of the deciduous tooth by reverse transcriptase-polymerase chain reaction (RT-PCR) and Northern blot analysis, and to identify MT1-MMP-producing cell during deciduous tooth resorption by in situ hybridization and immunohistochemistry. RT-PCR and Northern blot analysis revealed the exclusively high expression of MT1-MMP mRNA in bovine root-resorbing tissue, which lies between the root of the deciduous tooth and its permanent successor. Expression of MT1-MMP mRNA was seen in odontoclasts aligning in the surface layer of the root-resorbing tissue at sites of root resorption. Furthermore, immmunohistochemistry also confirmed the localization of MT1-MMP protein to the odontoclasts. The present identification of MT1-MMP in odontoclasts during deciduous tooth resorption might be relevant to the migration activity that these cells have to gain access to the root surface.

摘要

膜型1基质金属蛋白酶(MT1-MMP)是一种膜结合型基质金属蛋白酶,能够介导细胞外基质成分的细胞周围蛋白水解。在破骨细胞中,MT1-MMP的定位已报道在特殊膜突起(足体和片状伪足)的尖端,因此破骨细胞可能利用MT1-MMP进行局部蛋白水解,并穿过细胞外基质到达骨表面。本研究的目的是通过逆转录聚合酶链反应(RT-PCR)和Northern印迹分析来研究MT1-MMP在乳牙生理性牙根吸收中的相关性,并通过原位杂交和免疫组织化学鉴定乳牙吸收过程中产生MT1-MMP的细胞。RT-PCR和Northern印迹分析显示,MT1-MMP mRNA在牛牙根吸收组织中特异性高表达,该组织位于乳牙牙根与其恒牙胚之间。在牙根吸收部位的牙根吸收组织表层排列的破牙细胞中可见MT1-MMP mRNA的表达。此外,免疫组织化学也证实了MT1-MMP蛋白定位于破牙细胞。目前在乳牙吸收过程中破牙细胞中MT1-MMP的鉴定可能与这些细胞为接触牙根表面而必须具备的迁移活性有关。

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