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正畸牙齿移动过程中牙周韧带中的趋化因子 C-C 基元配体 8。

Chemokine C-C motif ligand 8 in periodontal ligament during orthodontic tooth movement.

机构信息

Department of Stomatology, Zhongshan Hospital, Fudan University, Shanghai 200032, China.

Department of Stomatology, Zhongshan Hospital, Fudan University, Shanghai 200032, China; State key laboratory of molecular engineering of polymers, Fudan University., Shanghai 200438, China.

出版信息

Arch Oral Biol. 2021 Mar;123:104996. doi: 10.1016/j.archoralbio.2020.104996. Epub 2021 Jan 10.

Abstract

OBJECTIVES

To investigate the roles of chemokine (C-C motif) ligand 8 (CCL8) in periodontal ligament during orthodontic tooth movement (OTM).

METHODS

Bioinformatics analyzed 100 genes in human periodontal ligament cells that were most upregulated after 48 hours of mechanical stress, and these genes were classified through GO and KEGG databases. Nickel-titanium closed-coil springs were placed between right first molar and incisors to produce 20 cN of orthodontic force in eight-week-old male SD rats for 1 and 2 days, followed by immunohistochemical staining of CCL8. Human periodontal ligament fibroblasts (hPDLFs) were stimulated by 14% cyclic tension force (Flexcell FX-5000 T Tension System) or hypoxia conditions to mimic OTM for 1 and 2 days, then the resulting CCL8 were examined through ELISA. Scratching assay was performed by treating hPDLFs with different concentrations of CCL8 (1 ng/ml, 10 ng/ml, 100 ng/ml). The migration, proliferation, and adhesion abilities of 100 ng/ml CCL8-treated hPDLFs were also examined. qRT-PCR and western blot detected matrix metalloproteinase 3, periostin, and osteoprotegrin expressions of hPDLFs under 100 ng/ml CCL8.

RESULTS

Bioinformatic analysis demonstrated that CCL8 was upregulated after applying mechanical stress for 48 hours. CCL8 secretion showed upregulation after 24 hours of OTM applicationsin vivo and in vitro. CCL8-treated hPDLFs showed significant positive effects on cell proliferation and matrix metalloproteinase 3. It also inhibited periostin and osteoprotegrin expressions.

CONCLUSIONS

CCL8 was upregulated in periodontal ligament during initial stage of OTM. Although CCL8 in human periodontal ligaments showed no significant effects on cell migration ability, it did enhance cell proliferation and osteoclastogenesis.

摘要

目的

探讨趋化因子(C-C 基序)配体 8(CCL8)在正畸牙齿移动(OTM)过程中牙周韧带中的作用。

方法

对机械应力作用 48 小时后牙周膜细胞中上调最明显的 100 个基因进行生物信息学分析,通过 GO 和 KEGG 数据库对这些基因进行分类。将镍钛封闭螺旋弹簧放置在 8 周龄雄性 SD 大鼠右侧第一磨牙和切牙之间,产生 20 cN 的正畸力,持续 1 和 2 天,然后进行 CCL8 免疫组织化学染色。用 14%循环张力力(Flexcell FX-5000T Tension System)或缺氧条件刺激人牙周膜成纤维细胞(hPDLFs),模拟 OTM 1 和 2 天,然后通过 ELISA 检测产生的 CCL8。用不同浓度的 CCL8(1ng/ml、10ng/ml、100ng/ml)处理 hPDLFs,进行划痕实验。还检测了 100ng/ml CCL8 处理的 hPDLFs 的迁移、增殖和黏附能力。qRT-PCR 和 Western blot 检测了 hPDLFs 在 100ng/ml CCL8 作用下基质金属蛋白酶 3、骨膜蛋白和护骨素的表达。

结果

生物信息学分析表明,施加机械力 48 小时后 CCL8 上调。体内和体外 OTM 应用 24 小时后,CCL8 分泌上调。CCL8 处理的 hPDLFs 对细胞增殖和基质金属蛋白酶 3 有显著的正向作用。它还抑制骨膜蛋白和护骨素的表达。

结论

在 OTM 的初始阶段,牙周韧带中 CCL8 上调。尽管人牙周韧带中的 CCL8 对细胞迁移能力没有显著影响,但它确实增强了细胞增殖和破骨细胞生成。

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