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牙龈卟啉单胞菌脂多糖抑制人牙周膜干细胞的成骨细胞分化并促进促炎细胞因子的产生。

Porphyromonas gingivalis LPS inhibits osteoblastic differentiation and promotes pro-inflammatory cytokine production in human periodontal ligament stem cells.

作者信息

Kato Hirohito, Taguchi Yoichiro, Tominaga Kazuya, Umeda Makoto, Tanaka Akio

机构信息

Department of Oral Pathology, Osaka Dental University, Osaka, Japan.

Department of Periodontology, Osaka Dental University, Osaka, Japan.

出版信息

Arch Oral Biol. 2014 Feb;59(2):167-75. doi: 10.1016/j.archoralbio.2013.11.008. Epub 2013 Nov 23.

DOI:10.1016/j.archoralbio.2013.11.008
PMID:24370188
Abstract

OBJECTIVE

Porphyromonas gingivalis (P. gingivalis) lipopolysaccharide (LPS) induces pro-inflammatory cytokines, such as interleukin-1 β (IL-1β), IL-6, and IL-8, which induce periodontal tissue destruction. Periodontal ligament stem cells (PDLSCs) play an important role in periodontal tissue regeneration and are expected to have future applications in cellular therapies for periodontitis. However, no studies have examined the effects of P. gingivalis LPS on PDLSCs. The aim of this study was to investigate how P. gingivalis LPS affects the osteoblastic differentiation and pro-inflammatory cytokine production of PDLSCs.

DESIGN

PDLSCs were obtained from healthy adult human mandibular third molars. The identification of PDLSCs was confirmed by immunohistochemical evaluations of the mesenchymal stem cell markers STRO-1 and SSEA-4. Cell proliferation and osteoblastic differentiation were investigated by culturing the PDLSCs in a normal or osteogenic medium with P. gingivalis LPS (0, 1, or 10μg/mL) and then measuring the alkaline phosphatase (ALP) activity and the production of collagen type 1 Alpha 1 (COL1A1), osteocalcin production, and mineralisation. Additionally, we examined the production of IL-1β, IL-6, and IL-8 in the PDLSCs.

RESULTS

P. gingivalis LPS inhibited the ALP activity, COL1A1 and osteocalcin production, and mineralisation in the PDLSCs, which are positive for STRO-1 and SSEA-4. P. gingivalis LPS also promoted cell proliferation and produced IL-1β, IL-6, and IL-8.

CONCLUSIONS

This study provides the first findings that P. gingivalis LPS inhibits osteoblastic differentiation and induces pro-inflammatory cytokines in PDLSCs. These findings will help clarify the relationship between periodontitis and periodontal tissue regeneration.

摘要

目的

牙龈卟啉单胞菌(P. gingivalis)脂多糖(LPS)可诱导促炎细胞因子,如白细胞介素 - 1β(IL - 1β)、IL - 6和IL - 8,这些细胞因子会导致牙周组织破坏。牙周膜干细胞(PDLSCs)在牙周组织再生中起重要作用,有望在未来用于牙周炎的细胞治疗。然而,尚无研究探讨牙龈卟啉单胞菌LPS对PDLSCs的影响。本研究旨在探究牙龈卟啉单胞菌LPS如何影响PDLSCs的成骨分化和促炎细胞因子产生。

设计

从健康成人下颌第三磨牙获取PDLSCs。通过对间充质干细胞标志物STRO - 1和SSEA - 4进行免疫组织化学评估来确认PDLSCs的鉴定。通过在含有牙龈卟啉单胞菌LPS(0、1或10μg/mL)的正常或成骨培养基中培养PDLSCs,然后测量碱性磷酸酶(ALP)活性、1型胶原蛋白α1(COL1A1)的产生、骨钙素的产生和矿化,来研究细胞增殖和成骨分化。此外,我们检测了PDLSCs中IL - 1β、IL - 6和IL - 8的产生。

结果

牙龈卟啉单胞菌LPS抑制了STRO - 1和SSEA - 4呈阳性的PDLSCs中的ALP活性、COL1A1和骨钙素的产生以及矿化。牙龈卟啉单胞菌LPS还促进了细胞增殖并产生IL - 1β、IL - 6和IL - 8。

结论

本研究首次发现牙龈卟啉单胞菌LPS抑制PDLSCs的成骨分化并诱导其产生促炎细胞因子。这些发现将有助于阐明牙周炎与牙周组织再生之间的关系。

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