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可溶性 E-钙黏蛋白:生殖道上皮损伤的标志物。

Soluble E-cadherin: A marker of genital epithelial disruption.

机构信息

Department of Medicine, University of Toronto, Toronto, Ontario, Canada.

Department of Microbiology and Immunology, Schulich School of Medicine and Dentistry, Western University, London, Ontario, Canada.

出版信息

Am J Reprod Immunol. 2023 Mar;89(3):e13674. doi: 10.1111/aji.13674. Epub 2023 Jan 12.

Abstract

PROBLEM

The genital epithelial barrier is a crucial first line of defence against HIV, and epithelial disruption may enhance HIV susceptibility. Assessment of genital epithelial integrity requires biopsies, but their collection is not practical in many research settings. A validated biomarker of genital epithelial barrier integrity would therefore be useful. The purpose of this study was to evaluate soluble E-cadherin (sE-cad) as a marker of genital epithelial disruption.

METHOD OF STUDY

Using in vitro models of endocervical and foreskin epithelial cells, we assessed changes in sE-cad, IL-6, IL-1β, and IL-1α levels following mechanical disruption. We also assessed changes in sE-cad levels in vivo in cervicovaginal secretions after epithelial disruption by endocervical cytobrush sampling in Canadian women, and assessed the relationship between levels of sE-cad in coronal sulcus swabs to membrane-bound E-cadherin in the overlying foreskin tissue in Ugandan men.

RESULTS

sE-cad levels immediately increased after in vitro epithelial physical disruption with the degree of elevation dependent on the extent of disruption, as did levels of IL-1β and IL-1α; this was followed by a delayed increase in IL-6 levels. In vivo results confirmed that sE-cad levels in cervicovaginal secretions were elevated 6 h after cytobrush sampling when compared to baseline. Furthermore, levels of sE-cad in the prepuce were inversely correlated with the amount of membrane-bound E-cadherin of overlying tissue.

CONCLUSION

Our results validate the use of sE-cad as a marker of epithelial disruption and demonstrate that the processes of physical disruption and inflammation in the genital tract are strongly intertwined.

摘要

问题

生殖道上皮屏障是抵抗 HIV 的第一道防线,而上皮细胞的破坏可能会增加 HIV 的易感性。评估生殖道上皮完整性需要进行活检,但在许多研究环境中采集活检并不实际。因此,一种经过验证的生殖道上皮屏障完整性的生物标志物将是有用的。本研究旨在评估可溶性 E-钙黏蛋白(sE-cad)作为生殖道上皮破坏的标志物。

研究方法

我们使用宫颈和包皮上皮细胞的体外模型,评估了机械破坏后 sE-cad、IL-6、IL-1β 和 IL-1α 水平的变化。我们还评估了加拿大女性在宫颈阴道分泌物中上皮破坏后 sE-cad 水平的变化,并评估了冠状沟拭子中 sE-cad 水平与乌干达男性包皮组织中膜结合型 E-钙黏蛋白之间的关系。

结果

sE-cad 水平在体外上皮物理破坏后立即升高,升高程度取决于破坏的程度,IL-1β 和 IL-1α 水平也随之升高;随后 IL-6 水平延迟升高。体内结果证实,与基线相比,宫颈阴道分泌物中的 sE-cad 水平在细胞刷取样后 6 小时升高。此外,包皮中的 sE-cad 水平与覆盖组织的膜结合型 E-钙黏蛋白的量呈反比。

结论

我们的结果验证了 sE-cad 作为上皮破坏标志物的使用,并表明生殖道中物理破坏和炎症过程是紧密交织在一起的。

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