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雌激素治疗对胶原酶诱导性关节炎骨髓细胞分化的影响。

Influence of estradiol treatment on bone marrow cell differentiation in collagenase-induced arthritis.

机构信息

Department of Immunology, Institute of Microbiology, Bulgarian Academy of Sciences, 1113, Sofia, Bulgaria.

Department of Biology, Medical Faculty, Medical University-Sofia, Sofia, Bulgaria.

出版信息

Inflamm Res. 2020 May;69(5):533-543. doi: 10.1007/s00011-020-01338-w. Epub 2020 Mar 21.

Abstract

OBJECTIVE AND DESIGN

Estrogen is one of the important regulators of the balance between bone formation and bone resorption that can modulate the levels and activity of certain growth factors and cytokines. In this study, we investigated the effect of 17β-estradiol (ED) on bone marrow (BM) cell differentiation in vivo and ex vivo in a mouse model of collagenase-induced osteoarthritis (CIOA).

SUBJECT

ICR (CD-2) female mice were used in present experiments (total number = 75) and bone marrow cells were used for in vitro studies.

TREATMENT

Mice were orally fed under different schemes with 17β-estradiol at a dose of 2 μg or 4 μg for 30 days.

METHODS

The effect of estradiol was estimated by histopathological, flow cytometry, and ELISA assays. Statistical differences were determined by one-way ANOVA.

RESULTS

Estradiol treatment ameliorated cartilage destruction and osteophyte formation if started from day 0 of CIOA induction, attended with a decrease of uterine and ovarian weights. Long time treatment lowered the percentage of megakaryocyte/platelet (CD62P+) populations and osteoclast (RANK+) populations in BM. Cells obtained from estradiol-treated CIOA mice showed inhibited capacity to differentiate into RANK+ and mesenchymal cells under osteoclastogenic conditions in vitro. Estrogen decreased serum IL-6 levels.

CONCLUSION

Results indicate a potential protective role for estrogen against the development of OA.

摘要

目的和设计

雌激素是调节骨形成和骨吸收平衡的重要调节因子之一,它可以调节某些生长因子和细胞因子的水平和活性。在本研究中,我们研究了 17β-雌二醇(ED)在胶原酶诱导性骨关节炎(CIOA)小鼠模型中体内和体外骨髓(BM)细胞分化中的作用。

对象

本实验使用 ICR(CD-2)雌性小鼠(总数为 75 只)和骨髓细胞进行体外研究。

治疗

根据不同方案,以 2μg 或 4μg 的剂量口服给予雌二醇 30 天。

方法

通过组织病理学、流式细胞术和 ELISA 检测评估雌二醇的作用。通过单因素方差分析确定统计学差异。

结果

如果从 CIOA 诱导的第 0 天开始进行雌二醇治疗,则可以改善软骨破坏和骨赘形成,并伴有子宫和卵巢重量降低。长期治疗可降低 BM 中巨核细胞/血小板(CD62P+)和破骨细胞(RANK+)群体的百分比。从接受雌二醇治疗的 CIOA 小鼠获得的细胞在体外破骨细胞生成条件下显示出抑制向 RANK+和间充质细胞分化的能力。雌激素降低了血清 IL-6 水平。

结论

结果表明雌激素对 OA 的发展具有潜在的保护作用。

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