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梅毒螺旋体Tp0751 通过促进 bEnd3 细胞凋亡和 IL-6 分泌改变紧密连接蛋白的表达。

Treponema pallidum Tp0751 alters the expression of tight junction proteins by promoting bEnd3 cell apoptosis and IL-6 secretion.

机构信息

Institution of Pathogenic Biology, Hengyang Medical College, University of South China, Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study, Hengyang 421001, China.

Affiliated Hengyang Hospital, Southern Medical University (Hengyang Central Hospital), Hengyang, Hunan 421000, China.

出版信息

Int J Med Microbiol. 2022 May;312(4):151553. doi: 10.1016/j.ijmm.2022.151553. Epub 2022 Mar 14.

Abstract

BACKGROUND

Neurosyphilis is a serious complication caused by the invasion of the central nervous system by Treponema pallidum subsp. pallidum (T. pallidum). However, the molecular mechanism by which T. pallidum crosses the blood-brain barrier has not been fully elucidated.

OBJECTIVES

The primary purpose of this experimental design was to explore the effect of the T. pallidum adhesion protein Tp0751 on the blood-brain barrier and cerebrovascular endothelial cells.

METHODS

BEnd3 cells were used to construct a monolayer blood-brain barrier model in vitro. The integrity of blood-brain barrier model was evaluated by a transendothelial cell resistance meter and transmission electron microscope after the stimulation of recombinant protein TP0751. Hoechst 33258 staining and flow cytometry were used to detect the apoptosis rate. Western blotting assay was used to measure the expression of tight junction proteins and apoptosis-related proteins. The enzyme activity detection kit was responsible for detecting the enzyme activities of Caspase 3, Caspase 8 and Caspase 9. The expression of pro-inflammatory cytokines TNF-α, IL-1β and IL-6 at the transcription and translation levels were detected by qRT-PCR and ELISA, respectively.

RESULTS

The results showed that, the tight junction structures between cells showed no obvious fragmentation, but the levels of the tight junction proteins zonula occludens-1 and occludin were reduced by the effects of Tp0751 on bEnd3 cells. In addition, further research demonstrated that after incubation with bEnd3 cells, Tp0751 induced cell apoptosis in a concentration- and time-dependent manner via the caspase 8/caspase 3 pathway. These apoptotic processes may have contributed to the changes in tight junction proteins expression. Furthermore, the Tp0751 protein may be involved in the pathogenic process by which T. pallidum crosses the blood-brain barrier by promoting secretion of the proinflammatory factor interleukin-6.

CONCLUSIONS

On the whole, this study is the first to reveal and highlight that Tp0751 may affect the expression of tight junction proteins by inducing apoptosis and promoting the secretion of the inflammatory cytokine IL-6, thus playing a role in the progression of neurosyphilis caused by T. pallidum.

摘要

背景

神经梅毒是由苍白密螺旋体亚种(苍白密螺旋体)侵犯中枢神经系统引起的严重并发症。然而,苍白密螺旋体穿越血脑屏障的分子机制尚未完全阐明。

目的

本实验设计的主要目的是探讨苍白密螺旋体粘附蛋白 Tp0751 对血脑屏障和脑血管内皮细胞的影响。

方法

采用 BEnd3 细胞在体外构建血脑屏障模型。重组蛋白 TP0751 刺激后,通过跨内皮细胞电阻仪和透射电镜评估血脑屏障模型的完整性。采用 Hoechst 33258 染色和流式细胞术检测细胞凋亡率。Western blot 检测紧密连接蛋白和凋亡相关蛋白的表达。酶活性检测试剂盒负责检测 Caspase 3、Caspase 8 和 Caspase 9 的酶活性。采用 qRT-PCR 和 ELISA 分别检测转录和翻译水平促炎细胞因子 TNF-α、IL-1β 和 IL-6 的表达。

结果

结果表明,细胞间紧密连接结构未见明显断裂,但 Tp0751 作用于 BEnd3 细胞后,紧密连接蛋白 zonula occludens-1 和 occludin 的水平降低。此外,进一步的研究表明,Tp0751 孵育 bEnd3 细胞后,通过 caspase 8/caspase 3 途径,以浓度和时间依赖的方式诱导细胞凋亡。这些凋亡过程可能导致紧密连接蛋白表达的变化。此外,Tp0751 蛋白可能通过促进促炎因子白细胞介素-6 的分泌,参与苍白密螺旋体穿越血脑屏障的致病过程。

结论

总的来说,本研究首次揭示和强调,Tp0751 可能通过诱导细胞凋亡和促进促炎细胞因子 IL-6 的分泌来影响紧密连接蛋白的表达,从而在苍白密螺旋体引起的神经梅毒进展中发挥作用。

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