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人脐带间充质干细胞通过调节巨噬细胞相关炎症因子缓解慢性输卵管炎。

Human Umbilical Cord Mesenchymal Stem Cells Alleviate Chronic Salpingitis by Modulating Macrophage-Associated Inflammatory Factors.

机构信息

Department of Obstetrics and Gynecology, Third Affiliated Hospital of Sun Yat-Sen University, 600, Tianhe Road, Tianhe District, Guangzhou, 510630, Guangdong, China.

出版信息

Curr Stem Cell Res Ther. 2024;19(11):1442-1448. doi: 10.2174/011574888X261128231108043931.

Abstract

INTRODUCTION

Mesenchymal stem cells (MSCs) have been widely studied because of their established anti-inflammatory properties. During chronic salpingitis (CS), infiltrated macrophages have vital roles in inflammation and tissue remodeling.

METHODS

We employed the type of MSCs, human umbilical cord (huc) MSCs in an experimental CS model and therapeutic efficacy was assessed. hucMSCs exerted this therapeutic effect by regulating macrophage function. To verify the regulatory effects of hucMSCs on the macrophage, macrophage line RAW264.7 markers were analyzed under LPS stimulation with or without co-culturing with hucMSCs for 12h and 24h. In addition, flow cytometry analysis was applied to reveal the interaction of co-culture. For animal studies, CS was induced by the MoPn strain Chlamydia trachomatis (CT), hucMSCs were intravaginally injected in the CS, and we analyzed the infiltrated macrophage by immunofluorescence.

RESULTS

We found the markers IL-10 was markedly increased and IL-1β, caspase-1 was notably downregulated after co-culturing with hucMSCs by RT-PCR. hucMSCs promote macrophage line RAW264.7 apoptosis. We also found that hucMSCs treatment can alleviate CS by decreasing the mRNA expression of IL-1β, caspase-1 and MCP-1 in the tubal tissue by RT-PCR and decreasing the protein expression of IL-1β, caspase-1 and TGF-β by western blotting.

CONCLUSION

These results suggest that macrophage function may be related to the immune-modulating characteristics of hucMSCs that contribute to CS.

摘要

简介

间充质干细胞(MSCs)因其具有明确的抗炎特性而被广泛研究。在慢性输卵管炎(CS)中,浸润的巨噬细胞在炎症和组织重塑中起着重要作用。

方法

我们在实验性 CS 模型中使用人脐带(huc)MSCs 类型,并评估其治疗效果。hucMSCs 通过调节巨噬细胞功能发挥这种治疗作用。为了验证 hucMSCs 对巨噬细胞的调节作用,在 LPS 刺激下,或在与 hucMSCs 共培养 12h 和 24h 后,分析巨噬细胞系 RAW264.7 标志物。此外,还应用流式细胞术分析来揭示共培养的相互作用。对于动物研究,通过莫庞氏菌属衣原体(CT)诱导 CS,将 hucMSCs 阴道内注射到 CS 中,并通过免疫荧光分析浸润的巨噬细胞。

结果

我们发现,通过 RT-PCR 分析,与 hucMSCs 共培养后,IL-10 标记物明显增加,IL-1β和 caspase-1 明显下调。hucMSCs 促进巨噬细胞系 RAW264.7 凋亡。我们还发现,hucMSCs 治疗可以通过降低输卵管组织中 IL-1β、caspase-1 和 MCP-1 的 mRNA 表达以及通过 Western blot 降低 IL-1β、caspase-1 和 TGF-β的蛋白表达来减轻 CS。

结论

这些结果表明,巨噬细胞功能可能与 hucMSCs 的免疫调节特性有关,这有助于 CS 的发生。

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