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牙髓卟啉单胞菌脂多糖对人牙髓细胞白细胞介素-1β产生的刺激作用。

Stimulation of interleukin-1 beta production of human dental pulp cells by Porphyromonas endodontalis lipopolysaccharide.

作者信息

Hosoya S, Matsushima K

机构信息

Department of Endodontics, Nihon University School of Dentistry at Matsudo, Chiba, Japan.

出版信息

J Endod. 1997 Jan;23(1):39-42. doi: 10.1016/S0099-2399(97)80205-1.

Abstract

IL-1 beta is synthesized as an inactive precursor, which is subsequently processed by IL-1 beta converting enzyme (ICE) and found extracellularly as a mature biologically active polypeptide. Also, IL-1 beta has been detected in necrotic and inflamed dental pulp. We examined the IL-1 beta production in human dental pulp (HDP) cells treated with lipopolysaccharide (LPS) from Porphyromonas endodontalis (P. e.) isolated from root canals and radicular cyst fluids. We demonstrated that P. e. LPS stimulated IL-1 beta release from HDP cells in a time- and dose-dependent manner. However, ICE activity was not increased by P. e. LPS. Northern blot hybridization analysis revealed that the IL-1 beta mRNA level in HDP cells was increased by P. e. LPS. These results suggest that stimulation of IL-1 beta release from HDP cells by P. e. LPS may have an important role in the progression of inflammation in pulpal and periapical disease.

摘要

白细胞介素-1β(IL-1β)最初以无活性前体的形式合成,随后由白细胞介素-1β转换酶(ICE)进行加工处理,并以成熟的生物活性多肽形式存在于细胞外。此外,在坏死和发炎的牙髓中也检测到了IL-1β。我们研究了用从根管和根尖囊肿液中分离出的牙髓卟啉单胞菌(P. e.)的脂多糖(LPS)处理人牙髓(HDP)细胞后IL-1β的产生情况。我们证明,P. e. LPS以时间和剂量依赖的方式刺激HDP细胞释放IL-1β。然而,P. e. LPS并未增加ICE的活性。Northern印迹杂交分析显示,P. e. LPS可使HDP细胞中的IL-1β mRNA水平升高。这些结果表明,P. e. LPS刺激HDP细胞释放IL-1β可能在牙髓和根尖周疾病炎症的进展中起重要作用。

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