The Roles of Angiotensin II in Stretched Periodontal Ligament Cells

被引:25
作者
Monnouchi, S. [2 ]
Maeda, H. [1 ]
Fujii, S. [1 ]
Tomokiyo, A. [2 ]
Kono, K. [2 ]
Akamine, A. [1 ,2 ]
机构
[1] Kyushu Univ Hosp, Dept Endodontol, Higashi Ku, Fukuoka 8128582, Japan
[2] Kyushu Univ, Fac Dent Sci, Dept Endodontol & Operat Dent, Div Oral Rehabil,Higashi Ku, Fukuoka 8128582, Japan
关键词
human periodontal ligament fibroblastic cells; stretch; angiotensin II; GENE-EXPRESSION; CARDIAC-HYPERTROPHY; MECHANICAL STRETCH; ENDOTHELIAL-CELLS; IN-VITRO; INCREASE; DIFFERENTIATION; FIBROBLASTS; RESORPTION; INDUCTION;
D O I
10.1177/0022034510382118
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
The loading caused by occlusion and mastication plays an important role in maintaining periodontal ligament (PDL) tissues. We hypothesized that a loading magnitude would be involved in the production of biological factors that function in the maintenance of PDL tissues. Here, we identified up-regulated gene expressions of transforming growth factor-beta 1 (TGF-beta 1), alkaline phosphatase (ALP), and angiotensinogen in human PDL fibroblastic cells (HPLFs) that were exposed to 8% stretch loading. Immunolocalization of angiotensin I/II (Ang I/II), which was converted from angiotensinogen, was detected in rat PDL tissues. HPLFs that were stimulated by Ang II also increased their gene expressions of TGF-beta 1 and ALP. Furthermore, the antagonist for Ang II type 2 receptor, rather than for type 1, significantly inhibited gene expressions induced by the stretch loading. Analysis of these data suggests that Ang II mediates the loading signal in stretched HPLFs to induce expressions of TGF-beta 1 and ALP.
引用
收藏
页码:181 / 185
页数:5
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