[人牙周韧带成纤维细胞(HPLF)磷酸酪氨酸磷酸酶活性研究]。

Y Ishiwata
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引用次数: 0

摘要

牙周韧带是一种非钙化的结缔组织,参与与咬合和咀嚼等机械应力相关的重塑过程。本研究旨在探讨磷酸酪氨酸磷酸酶(PTPase)在人牙周韧带成纤维细胞(HPLF)细胞附着和扩散中的作用。用维生素D3 (D3)和地塞米松(Dex)培养人牙周韧带外植体HPLF 12 d。培养第7天,分别以磷酸酪氨酸和对硝基苯基磷酸为底物测定PTPase和ALPase活性。虽然D3和Dex显著提高了HPLF的ALPase活性,但PTPase活性没有改变。用无血清MCDB 107培养静止HPLF后,将HPLF条件培养基(HPLF- cm)包被于疏水性培养皿上。然后用32Pi在培养皿上接种培养HPLF。与对照培养基相比,HPLF的PTPase活性降低,但在培养基中添加32Pi的掺入量增加了2倍。因此,HPLF具有PTPase,它可以使磷酸化蛋白的磷酸化酪氨酸去磷酸化,从而调节细胞增殖。HPLF-CM中含有的细胞附着因子和扩散因子可能改变磷酸化蛋白的磷酸化和去磷酸化过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Phosphotyrosine phosphatase activity of human periodontal ligament fibroblasts (HPLF)].

The periodontal ligament is a non-calcified connective tissue involved in the remodeling processes associated with mechanical stresses such as occlusion and mastication. This study was attempted to explore the characterization of phosphotyrosine phosphatase (PTPase) on the cell attachment and spreading of human periodontal ligament fibroblasts (HPLF). HPLF obtained by the explantation of human periodontal ligaments were cultured with vitamin D3 (D3) and dexamethasone (Dex) for 12 days. At 7 day culture, PTPase and ALPase activities were assayed with the substrates of phosphotyrosine and p-nitrophenylphosphate, respectively. Although ALPase activity of HPLF was dramatically increased by D3 and Dex, PTPase activity was not altered. After the quiescent HPLF were cultured with serum-free MCDB 107, the conditioned medium of HPLF (HPLF-CM) was coated on a hydrophobic dish. And then, HPLF were inoculated and cultured with 32Pi on the dish. PTPase activity of HPLF was decreased compared with control medium, however, the incorporation of 32Pi added in the medium was increased 2-fold. Therefore, HPLF possess the PTPase which may dephosphorylate a phosphotyrosine of phosphoproteins, which can regulate the cell proliferation. The cell attachment and spreading factors contained in HPLF-CM might alter the processes of phosphorylation and dephosphorylation of phosphoproteins.

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