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评价 TNF-α 和 IFN-γ 预刺激骨髓间充质干细胞条件培养液对乙酸诱导的小鼠急性结肠炎模型的作用。

Evaluation of TNF-α and IFN-γ primed conditioned medium of mesenchymal stem cell in acetic acid-induced mouse model of acute colitis.

机构信息

Department of Immunology, School of Medicine, Mazandaran University of Medical Sciences, Sari, IRAN; Immunogenetics Research Center, Mazandaran University of Medical Sciences, Sari, Iran.

Anatomical Research Center, Kashan University of Medical Sciences and Health Services, kashan, IRAN.

出版信息

Cell Immunol. 2024 Nov-Dec;405-406:104876. doi: 10.1016/j.cellimm.2024.104876. Epub 2024 Sep 24.

Abstract

IBD, an autoimmune-inflammatory disorder that affects people who are genetically prone to inflammation. There is a lot of interest in MSC-CM therapy, especially when primed with TNF-α + IFN-γ. Throughout the study, data were collected on the percentage of apoptotic cells, gene expression of ZO-1, Foxp3, GATA3, IDO-1, Muc2, T-bet, Notch1, TNFR2, and ROR-γt, colon weight and length, histopathological analysis, and DAI. TNF-α and IL-10 levels were assessed in addition to the NO level. The results suggest that primed MSC-CM improved DAI, mucosal deterioration, intestinal inflammation and NO concentration. The amount of TNF-α was decreased, but IL-10 and the colon's percentage of apoptotic cells was increased. The mRNA expression of ZO-1, Foxp3, GATA3, IDO-1, and Muc2 genes increased greatly in the treatment groups, while the expression of T-bet, Notch1, TNFR2, and ROR-γt genes has decreased. These studies suggest that primed MSC-CM may combine with common treatments to improve responsiveness.

摘要

IBD,一种自身免疫性炎症性疾病,影响那些易患炎症的遗传倾向人群。MSC-CM 疗法备受关注,特别是在 TNF-α+IFN-γ 预激活后。在整个研究过程中,收集了凋亡细胞的百分比、ZO-1、Foxp3、GATA3、IDO-1、Muc2、T-bet、Notch1、TNFR2 和 ROR-γt 的基因表达、结肠重量和长度、组织病理学分析和 DAI 的数据。除了 NO 水平外,还评估了 TNF-α 和 IL-10 水平。结果表明,预激活的 MSC-CM 改善了 DAI、黏膜恶化、肠道炎症和 NO 浓度。TNF-α 含量减少,但 IL-10 和结肠凋亡细胞的百分比增加。治疗组中 ZO-1、Foxp3、GATA3、IDO-1 和 Muc2 基因的 mRNA 表达大大增加,而 T-bet、Notch1、TNFR2 和 ROR-γt 基因的表达则减少。这些研究表明,预激活的 MSC-CM 可能与常规治疗相结合,以提高反应性。

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