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[脂多糖对人牙周膜干细胞增殖及炎症因子表达的影响]

[Effect of lipopolysaccharide on proliferation and inflammatory factors expression of human periodontal ligament stem cells].

作者信息

Wang Lan, Xia Jiajia, Liu Qi, Jin Yan

机构信息

Dept. of Conservative Dentistry and Endodontics, The Affiliated Hospital of Stomatology, Chongqing Medical University, China.

出版信息

Hua Xi Kou Qiang Yi Xue Za Zhi. 2013 Jun;31(3):286-90.

Abstract

OBJECTIVE

To investigate the effect of Porphyromonas gingivalis lipopolysaccharide (LPS) on proliferation and inflammatory factors expression of human periodontal ligament stem cells (HPDLSCs).

METHODS

HPDLSCs were cultivated and identified. Experiment was divided into 3 groups according to culture solution: Group A with alpha-MEM culture solution containing 10 microg.mL-1 LPS, group B with supernatant fluid containing 10ng.mL-1 LPS stimulated monocyte, group C with alpha-MEM culture solution. The proliferation ability of HPDLSCs was analyzed by MTF assay. The expression levels of interleukin-1beta (IL-1beta), interleukin-6 (IL-6), tumor necrosis factor (TNF-alpha) mRNA of HPDLSCs were detected by reverse transcriptase polymerase chain reaction(RT-PCR).

RESULTS

HPDLSCs had clonality, bone and fat differentiation ability. Compared with group C, the proliferation ability of HPDLSCs of group A and group B was significantly inhibited, and the proliferation ability of HPDLSCs of group B were more significantly inhibited than that of group A (P<0.05). The expression of IL-1beta, IL-6 and TNF-alpha mRNA of group A and group B increased compared with the control group, and the expression of IL-1beta, IL-6 and TNF-alpha mRNA of group B increased more than that of group A (P<0.05).

CONCLUSION

Porphyromonas gingivalis may inhibit the proliferation of HPDLSCs directly or indirectly through LPS and increase expression of inflammatory factor, exacerbate periodontal inflammatory tissue damage and delay the self-repairing of periodontal tissue.

摘要

目的

探讨牙龈卟啉单胞菌脂多糖(LPS)对人牙周膜干细胞(HPDLSCs)增殖及炎症因子表达的影响。

方法

培养并鉴定HPDLSCs。根据培养液将实验分为3组:A组为含10μg/mL LPS的α-MEM培养液,B组为含10ng/mL LPS刺激单核细胞的上清液,C组为α-MEM培养液。采用MTT法分析HPDLSCs的增殖能力。通过逆转录聚合酶链反应(RT-PCR)检测HPDLSCs白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)、肿瘤坏死因子(TNF-α)mRNA的表达水平。

结果

HPDLSCs具有克隆性、成骨及成脂分化能力。与C组比较,A组和B组HPDLSCs的增殖能力明显受到抑制,且B组HPDLSCs的增殖能力比A组受到更明显的抑制(P<0.05)。与对照组比较,A组和B组IL-1β、IL-6及TNF-α mRNA的表达增加,且B组IL-1β、IL-6及TNF-α mRNA的表达比A组增加更明显(P<0.05)。

结论

牙龈卟啉单胞菌可能通过LPS直接或间接抑制HPDLSCs的增殖并增加炎症因子表达,加重牙周炎症组织损伤,延缓牙周组织的自我修复。

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