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低剂量伴放线放线杆菌脂多糖预处理对人全血细胞因子产生的影响。

Effect of low dose Actinobacillus actinomycetemcomitans lipopolysaccharide pretreatment on cytokine production by human whole blood.

作者信息

Nakamura Tsutomu, Nitta Hiroshi, Ishikawa Isao

机构信息

Periodontology, Department of Hard Tissue Engineering, Graduate School, Tokyo Medical and Dental University, Tokyo, Japan.

出版信息

J Periodontal Res. 2004 Apr;39(2):129-35. doi: 10.1111/j.1600-0765.2004.00717.x.

Abstract

BACKGROUND AND OBJECTIVE

Periodontal disease is known to influence the systemic condition in various ways, and the bacteria and their products, such as lipopolysaccharides (LPS), may spread from periodontal lesions via the systemic circulation to affect distant organs. The level of LPS in plasma from such patients is reported to be very low, and this low level of LPS is suspected to have priming or desensitizing effect. Thus, we investigated the effects of low dose LPS pretreatment on LPS-dependent cytokine production by whole blood cells ex vivo.

METHODS

Blood samples obtained from seven systemically and periodontally healthy individuals were pretreated with or without 5 pg/ml Actinobacillus actinomycetemcomitans LPS, followed by further stimulation with 1 ng/ml A. actinomycetemcomitans LPS. The concentrations of interleukin-1 beta (IL-1beta), IL-6, IL-10 and tumor necrosis factor-alpha (TNF-alpha) in the culture supernatants were then determined using enzyme-linked immunosorbent assay (ELISA). In addition, intracytoplasmic cytokine staining of whole blood cells was performed for flow cytometry.

RESULTS

Pretreatment with 5 pg/ml A. actinomycetemcomitans LPS significantly enhanced the production of IL-1beta and IL-6 from whole blood when further induced by 1 ng/ml LPS (1.72 times higher for IL-1beta, 2.18 times higher for IL-6 than without pretreatment). The pretreatment did not enhance the production of either TNF-alpha or IL-10. Intracytoplasmic staining showed that the monocyte fraction was primarily involved in producing IL-1beta and IL-6. Flow cytometric analysis revealed that pretreatment increased the number of IL-1beta and IL-6 producing cells as well as mean fluorescence intensity of the stained cells.

CONCLUSION

A low dose of bloodstream LPS found in periodontitis patients appears to be sufficient to prime monocytes, and may be capable of affecting the systemic responses of immune and inflammatory cells.

摘要

背景与目的

已知牙周疾病会以多种方式影响全身状况,细菌及其产物,如脂多糖(LPS),可能从牙周病变处经体循环扩散至远处器官。据报道,此类患者血浆中的LPS水平非常低,且怀疑这种低水平的LPS具有启动或脱敏作用。因此,我们研究了低剂量LPS预处理对全血细胞体外LPS依赖性细胞因子产生的影响。

方法

从7名全身和牙周健康的个体采集血样,分别用或不用5 pg/ml伴放线放线杆菌LPS进行预处理,随后再用1 ng/ml伴放线放线杆菌LPS进一步刺激。然后使用酶联免疫吸附测定(ELISA)法测定培养上清液中白细胞介素-1β(IL-1β)、IL-6、IL-10和肿瘤坏死因子-α(TNF-α)的浓度。此外,对全血细胞进行胞内细胞因子染色以进行流式细胞术分析。

结果

用5 pg/ml伴放线放线杆菌LPS预处理后,当再用1 ng/ml LPS进一步诱导时,全血中IL-1β和IL-6的产生显著增强(IL-1β比未预处理时高1.72倍,IL-6高2.18倍)。该预处理未增强TNF-α或IL-10的产生。胞内染色显示单核细胞部分主要参与IL-1β和IL-6的产生。流式细胞术分析表明,预处理增加了产生IL-1β和IL-6的细胞数量以及染色细胞的平均荧光强度。

结论

牙周炎患者血液中低剂量的LPS似乎足以启动单核细胞,并可能影响免疫和炎症细胞的全身反应。

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