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PGE2抑制TDO2表达和活性调控巨噬细胞功能变化的机制OA北大核心CSTPCD

The specific mechanism of PGE2 inhibiting TDO2 expression and activity regulation of macrophage function changes

中文摘要英文摘要

目的 探究色氨酸-2,3-双加氧酶(TDO2)在胶原诱导型关节炎(CIA)小鼠中的表达以及前列腺素E2(PGE2)抑制TDO2表达和活性调控巨噬细胞功能的机制.方法 Ⅱ型胶原诱导DBA/1J小鼠制备CIA模型.X射线检测CIA小鼠踝关节损伤变化;免疫组化检测小鼠踝关节、脾脏中TDO2表达;qPCR和免疫荧光检测小鼠腹腔巨噬细胞中TDO2表达变化.通过在RAW264.7细胞中分别小干扰TDO2、给予TDO2抑制剂680C91、给予不同浓度PGE2(0.1、1、10 μmol/L)刺激和给予前列腺素受体4(EP4)激动剂 CAY10598 后,qPCR 和 Western blot 检测 TDO2 表达;流式细胞术检测巨噬细胞吞噬和极化功能;比色法检测TDO2活性.结果 与正常组小鼠比较,CIA小鼠踝关节软组织肿胀变大,关节滑膜、脾脏及腹腔巨噬细胞中TDO2表达增加.在RAW264.7细胞中分别小干扰TDO2、给予TDO2抑制剂680C91、给予PGE2刺激、给予EP4受体激动剂CAY10598后TDO2表达明显被抑制,巨噬细胞吞噬功能下降,M1/M2比值下降(P<0.05);比色法结果显示RAW264.7细胞中分别给予PGE2刺激以及EP4激动剂CAY10598后TDO2的活性被抑制(P<0.05).结论 巨噬细胞TDO2表达升高可能促进了 CIA小鼠关节滑膜损伤,PGE2通过激活EP4受体抑制TDO2表达和活性从而调节巨噬细胞功能.

Objective To investigate the effects of tryptophan-2,3-dioxygenase(TDO2)on collagen-induced ar-thritis,the expression of CIA in mice and the specific mechanism by which prostaglandin E2(PGE2)inhibits the expression and activity of TDO2 and thus regulates the function of macrophages.Methods Type Ⅱ collagen in-duced the CIA model in DBA/1J mice.The ankle joint injury of CIA mice was detected by X-ray.The expression of TDO2 in ankle joint and spleen was detected by immunohistochemistry.Changes of TDO2 expression in perito-neal macrophages(PMs)were detected by qPCR and immunofluorescence.TDO2 expression was detected by small interference in RAW264.7 cells,TDO2 inhibitor 680C91,PGE2 stimulation with different concentrations(0.1,1,10 μmol/L)and EP4 receptor agonist CAY10598.qPCR and Western blot were used to detect TDO2 expression.The phagocytosis and polarization of macrophages were detected by flow cytometry.The activity of TDO2 was detec-ted by colorimetry.Results Compared with normal mice,CIA mice had larger soft tissue swelling in ankle,and increased TDO2 expression in synovium,spleen and PMs.In RAW264.7 cells,TDO2 expression was significantly inhibited after small interference,TDO2 inhibitor 680C91,PGE2 stimulation,and EP4 receptor agonist CAY10598,macrophage phagocytosis decreased,and M1/M2 ratio decreased(P<0.05).Colorimetric results showed that the activity of TDO2 was inhibited after stimulation of PGE2 and EP4 agonist CAY10598 in RAW264.7 cells(P<0.05).Conclusion The increased expression of TDO2 in macrophages may promote synovial injury in CIA mice,and PGE2 regulates the function of macrophages by inhibiting the expression and activity of TDO2 by ac-tivating EP4 receptor.

王燚;李丝雨;王越业;董伟波;程梦;魏伟;常艳

安徽医科大学临床药理研究所,抗炎免疫药物教育部重点实验室,安徽省抗炎免疫药物协同创新中心,安徽医科大学类风湿关节炎研究中心,合肥 230032

临床医学

类风湿关节炎胶原诱导型关节炎色氨酸-2,3-双加氧酶前列腺素E2前列腺素受体4

rheumatoid arthritiscollagen-induced arthritistryptophan-2,3-dioxygenaseprostaglandin E2prostaglandin receptor 4

《安徽医科大学学报》 2024 (007)

1107-1115 / 9

安徽省自然科学基金面上项目(编号:2108085MH320);安徽省留学人员创新项目择优资助计划项目(编号:200LCX019)

10.19405/j.cnki.issn1000-1492.2024.07.001

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