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根囊肿中的成纤维细胞通过富含外显子 A 的纤维连接蛋白的自分泌作用促进破骨细胞生成。

The fibroblast of radicular cyst facilitate osteoclastogenesis via the autocrine of Fibronectin containing extra domain A.

机构信息

Department of Endodontics, School & Hospital of Stomatology, Shanghai Engineering Research Center of Tooth Restoration and Regeneration, Tongji University, Shanghai, China.

Department of Pathology, School & Hospital of Stomatology, Shanghai Engineering Research Center of Tooth Restoration and Regeneration, Tongji University, Shanghai, China.

出版信息

Oral Dis. 2019 May;25(4):1136-1146. doi: 10.1111/odi.13064. Epub 2019 Mar 18.

Abstract

OBJECTIVE

To investigate the alternative spliced isoforms of Fibronectin (FN) in the stroma of radicular cysts and analyze the associations between these isoforms and the osteoclastogenic effects of fibroblasts.

METHODS AND MATERIALS

The specimens of radicular cysts were stained with immunohistochemistry, and the associations between each FN isoform and clinical parameters were assessed. The fibroblasts isolated from cysts or jaw bone were cultured to induce the Trap + MNCs. In the conditioned medium, the Fibronectin containing extra domain A (EDA + FN) was neutralized by antibody IST-9, and the EDA exon of fibroblasts was knockout by CRISPR/Cas system, for assessing the osteoclastogenic effects. The mRNA level of FN isoforms and the osteoclastogenesis-related genes were analyzed by quantitive PCR.

RESULTS

EDA + FN staining was positively associated with the size of the lesions (p < 0.05). In contrast with the controls, the ratio of EDA + FN/total FN in the fibroblasts from radicular cysts was significantly higher (p < 0.05), and positively associate with Trap + MNCs counting, it was consistent with increased expression of COX-2, IL-6, IL-17, and the RANKL/OPG (p < 0.05). The Trap + MNCs counting and osteoclastogenesis-related genes were decreased by IST-9 blocking and EDA exon knockout in fibroblasts, but the blockage of the interaction between EDA + FN and pre-osteoclasts exhibited little effects on Trap + MNCs formation.

CONCLUSION

The microenvironment of the fibrous capsule of radicular cysts facilitates the splicing of EDA exon, it endues EDA + FN with autocrine effects on fibroblast itself, and it increases the expression of osteoclastogenesis-related genes, by which the osteoclastogenesis in radicular cysts could be initiated.

摘要

目的

研究根囊肿基质中纤维连接蛋白(FN)的选择性剪接异构体,并分析这些异构体与成纤维细胞破骨细胞生成作用的关系。

方法与材料

对根囊肿标本进行免疫组织化学染色,并评估每种 FN 异构体与临床参数之间的关系。从囊肿或颌骨中分离出成纤维细胞进行培养,以诱导破骨细胞前体细胞(Trap+MNCs)形成。在条件培养基中,用抗体 IST-9 中和含有额外结构域 A(EDA+FN)的纤维连接蛋白,并通过 CRISPR/Cas 系统敲除成纤维细胞的 EDA 外显子,以评估破骨细胞生成作用。通过定量 PCR 分析 FN 异构体和破骨细胞生成相关基因的 mRNA 水平。

结果

EDA+FN 染色与病变大小呈正相关(p<0.05)。与对照组相比,根囊肿来源的成纤维细胞中 EDA+FN/总 FN 的比值明显升高(p<0.05),与 Trap+MNCs 计数呈正相关,与 COX-2、IL-6、IL-17 和 RANKL/OPG 的表达增加一致(p<0.05)。用 IST-9 阻断和 EDA 外显子敲除成纤维细胞后,Trap+MNCs 计数和破骨细胞生成相关基因表达减少,但阻断 EDA+FN 与破骨细胞前体之间的相互作用对 Trap+MNCs 形成的影响很小。

结论

根囊肿纤维囊的微环境促进 EDA 外显子的剪接,赋予 EDA+FN 对成纤维细胞自身的自分泌作用,并增加破骨细胞生成相关基因的表达,从而启动根囊肿中的破骨细胞生成。

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