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TGF-β2 在炎症条件下下调牙周膜干细胞的成骨作用。

TGF-β2 downregulates osteogenesis under inflammatory conditions in dental follicle stem cells.

机构信息

Biotooth Engineering Lab, Dental Research Institute, Dental Regenerative Biotechnology, Department of Dental Science, School of Dentistry, Seoul National University, Seoul, Korea.

Biotooth Engineering Lab, Department of Oral and Maxillofacial Surgery and Craniomaxillofacial Life Science, Dental Research Institute, School of Dentistry, Seoul National University, Seoul, Korea.

出版信息

Int J Oral Sci. 2018 Oct 9;10(3):29. doi: 10.1038/s41368-018-0028-8.

Abstract

Bone formation is important for the reconstruction of bone-related structures in areas that have been damaged by inflammation. Inflammatory conditions such as those that occur in patients with rheumatoid arthritis, cystic fibrosis, and periodontitis have been shown to inhibit osteoblastic differentiation. This study focussed on dental follicle stem cells (DFSCs), which are found in developing tooth germ and participate in the reconstruction of alveolar bone and periodontal tissue in periodontal disease. After bacterial infection of inflamed dental tissue, the destruction of bone was observed. Currently, little is known about the relationship between the inflammatory environment and bone formation. Osteogenic differentiation of inflamed DFSCs resulted in decreased alkaline phosphatase (ALP) activity and alizarin red S staining compared to normal DFSCs. Additionally, in vivo transplantation of inflamed and normal DFSCs demonstrated severe impairment of osteogenesis by inflamed DFSCs. Protein profile analysis via liquid chromatography coupled with tandem mass spectrometry was performed to analyse the differences in protein expression in inflamed and normal tissue. Comparison of inflamed and normal DFSCs showed significant changes in the level of expression of transforming growth factor (TGF)-β2. Porphyromonas gingivalis (P.g.)-derived lipopolysaccharide (LPS) was used to create in vitro inflammatory conditions similar to periodontitis. The osteogenic differentiation of LPS-treated DFSCs was suppressed, and the cells displayed low levels of TGF-β1 and high levels of TGF-β2. DFSCs treated with TGF-β2 inhibitors showed significant increases in alizarin red S staining and ALP activity. TGF-β1 expression was also increased after inhibition of TGF-β2. By examining inflamed DFSCs and LPS-triggered DFSCs, these studies showed both clinically and experimentally that the increase in TGF-β2 levels that occurs under inflammatory conditions inhibits bone formation.

摘要

成骨对于炎症损伤区域相关骨结构的重建非常重要。类风湿关节炎、囊性纤维化和牙周炎等炎症性疾病已被证实会抑制成骨细胞分化。本研究聚焦于牙囊干细胞(DFSCs),其存在于发育中的牙胚中,并参与牙周病中牙槽骨和牙周组织的重建。在受细菌感染的发炎牙组织中,观察到了骨破坏。目前,人们对炎症环境与骨形成之间的关系知之甚少。与正常 DFSCs 相比,炎症 DFSCs 的成骨分化导致碱性磷酸酶(ALP)活性和茜素红 S 染色降低。此外,体内移植炎症和正常 DFSCs 表明炎症 DFSCs 严重损害了成骨作用。通过液相色谱-串联质谱联用技术进行蛋白质谱分析,以分析炎症和正常组织中蛋白质表达的差异。比较炎症和正常 DFSCs 显示转化生长因子(TGF)-β2 的表达水平有显著变化。牙龈卟啉单胞菌(P.g.)衍生的脂多糖(LPS)用于体外模拟类似牙周炎的炎症条件。LPS 处理的 DFSCs 的成骨分化受到抑制,细胞中 TGF-β1 水平降低,TGF-β2 水平升高。用 TGF-β2 抑制剂处理的 DFSCs 茜素红 S 染色和 ALP 活性显著增加。抑制 TGF-β2 后 TGF-β1 的表达也增加。通过研究炎症 DFSCs 和 LPS 触发的 DFSCs,这些研究从临床和实验两方面表明,炎症条件下 TGF-β2 水平的升高抑制了骨形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6423/6175959/3d1ddfb76c56/41368_2018_28_Fig1_HTML.jpg

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