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IL-22 通过增强紧密连接并协调细胞外基质来调节子宫内膜再生。

IL-22 regulates endometrial regeneration by enhancing tight junctions and orchestrating extracellular matrix.

机构信息

Center for Cancer Cell Biology, Immunology, and Infection, Rosalind Franklin University of Medicine and Science, North Chicago, IL, United States.

Clinical Immunology Laboratory, Rosalind Franklin University of Medicine and Science, North Chicago, IL, United States.

出版信息

Front Immunol. 2022 Aug 25;13:955576. doi: 10.3389/fimmu.2022.955576. eCollection 2022.

Abstract

The uterine endometrium uniquely regenerates after menses, postpartum, or after breaks in the uterine layer integrity throughout women's lives. Direct cell-cell contacts ensured by tight and adherens junctions play an important role in endometrial integrity. Any changes in these junctions can alter the endometrial permeability of the uterus and have an impact on the regeneration of uterine layers. Interleukin 22 (IL-22) is a cytokine that is recognized for its role in epithelial regeneration. Moreover, it is crucial in controlling the inflammatory response in mucosal tissues. Here, we studied the role of IL-22 in endometrial recovery after inflammation-triggered abortion. Fecundity of mice was studied in consecutive matings of the same animals after lipopolysaccharide (LPS) (10 µg per mouse)-triggered abortion. The fecundity rate after the second mating was substantially different between IL-22 knockout (IL-22) (9.1%) and wild-type (WT) (71.4%) mice (p < 0.05), while there was no difference between the groups in the initial mating, suggesting that IL-22 deficiency might be associated with secondary infertility. A considerable difference was observed between IL-22 and WT mice in the uterine clearance following LPS-triggered abortion. Gross examination of the uteri of IL-22 mice revealed non-viable fetuses retained inside the horns (delayed clearance). In contrast, all WT mice had completed abortion with total clearance after LPS exposure. We also discovered that IL-22 deficiency is associated with a decreased expression of tight junctions (claudin-2 and claudin-10) and cell surface pathogen protectors (mucin-1). Moreover, IL-22 has a role in the remodeling of the uterine tissue in the inflammatory environment by regulating epithelial-mesenchymal transition markers called E- and N-cadherin. Therefore, IL-22 contributes to the proper regeneration of endometrial layers after inflammation-triggered abortion. Thus, it might have a practical significance to be utilized as a treatment option postpartum (enhanced regeneration function) and in secondary infertility caused by inflammation (enhanced barrier/protector function).

摘要

子宫内膜在女性的一生中,在月经、产后或子宫层完整性中断后会独特地再生。紧密连接和黏附连接所确保的直接细胞-细胞接触在子宫内膜完整性中发挥重要作用。这些连接的任何变化都可能改变子宫的子宫内膜通透性,并对子宫层的再生产生影响。白细胞介素 22 (IL-22) 是一种细胞因子,其作用已得到公认,可促进上皮细胞再生。此外,它在控制粘膜组织的炎症反应中也很关键。在这里,我们研究了白细胞介素 22 在炎症触发流产后子宫内膜恢复中的作用。通过脂多糖 (LPS) (每只小鼠 10 µg) 触发流产后连续同种动物交配来研究小鼠的生育能力。第二次交配后的生育能力在白细胞介素 22 敲除 (IL-22) (9.1%) 和野生型 (WT) (71.4%) 小鼠之间有显著差异 (p < 0.05),而在初次交配中两组之间没有差异,这表明 IL-22 缺乏可能与继发性不孕有关。在 LPS 触发流产后,IL-22 和 WT 小鼠的子宫清除率有明显差异。IL-22 小鼠子宫的大体检查显示,有未存活的胎儿残留在角内 (清除延迟)。相比之下,所有 LPS 暴露的 WT 小鼠都已完全流产,子宫完全清除。我们还发现,IL-22 缺乏与紧密连接 (claudin-2 和 claudin-10) 和细胞表面病原体保护剂 (粘蛋白-1) 的表达减少有关。此外,IL-22 通过调节上皮-间充质转化标志物 E-和 N-钙黏蛋白在炎症环境中发挥重塑子宫组织的作用。因此,IL-22 有助于炎症触发流产后子宫内膜层的适当再生。因此,它可能具有实际意义,可作为产后的治疗选择 (增强再生功能) 和炎症引起的继发性不孕的治疗选择 (增强屏障/保护功能)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edf6/9453595/dd9b8e23ef84/fimmu-13-955576-g001.jpg

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