Schepens Eye Research Institute, Massachusetts Eye and Ear Infirmary, Department of Ophthalmology, Harvard Medical School, Boston, Massachusetts.
Center for Experimental Therapeutics and Reperfusion Injury, Brigham and Women's Hospital and Department of Anaesthesia, Perioperative and Pain Medicine, Harvard Medical School, Boston, Massachusetts.
Am J Pathol. 2020 Sep;190(9):1823-1832. doi: 10.1016/j.ajpath.2020.06.001. Epub 2020 Jun 16.
Leukotriene B4 (LTB4) is a major proinflammatory mediator important in host defense, whereas resolvins (Rvs) are produced during the resolution phase of inflammation. The authors determined the actions of both RvE1 and RvD1 on LTB4-induced responses of goblet cells cultured from rat conjunctiva. The responses measured were an increase in the intracellular [Ca] ([Ca]) and high-molecular-weight glycoprotein secretion. Treatment with RvE1 or RvD1 for 30 minutes significantly blocked the LTB4-induced [Ca] increase. The actions of RvE1 on LTB4-induced [Ca] increase were reversed by siRNA for the RvE1 receptor, and the actions of RvD1 were reversed by an RvD1 receptor inhibitor. The RvE1 and RvD1 block of LTB4-stimulated increase in [Ca] was also reversed by an inhibitory peptide to β-adrenergic receptor kinase. LTB4 and block of the LTB4-stimulated increase in [Ca] by RvE1 and RvD1 were partially mediated by the depletion of intracellular Ca stores. RvE1, but not RvD1, counterregulated the LTB4-induced high-molecular-weight glycoprotein secretion. Thus, both RvE1 and RvD1 receptors directly inhibit LTB4 by phosphorylating the LTB4 receptor using β adrenergic receptor kinase. RvE1 receptor counterregulates the LTB4-induced increase in [Ca] and secretion, whereas RvD1 receptor only counterregulates LTB4-induced [Ca] increase.
白三烯 B4(LTB4)是宿主防御中重要的主要促炎介质,而消退素(Rvs)是在炎症消退阶段产生的。作者确定了 RvE1 和 RvD1 对从大鼠结膜培养的杯状细胞中 LTB4 诱导的反应的作用。测量的反应是细胞内[Ca]([Ca])和高分子量糖蛋白分泌的增加。用 RvE1 或 RvD1 处理 30 分钟可显著阻断 LTB4 诱导的[Ca]增加。RvE1 对 LTB4 诱导的[Ca]增加的作用可被 RvE1 受体的 siRNA 逆转,而 RvD1 的作用可被 RvD1 受体抑制剂逆转。RvE1 和 RvD1 对 LTB4 刺激的[Ca]增加的阻断也可被β肾上腺素能受体激酶的抑制肽逆转。LTB4 和 RvE1 和 RvD1 对 LTB4 刺激的[Ca]增加的阻断部分是通过细胞内 Ca 库耗竭介导的。RvE1 但不是 RvD1,通过使用β肾上腺素能受体激酶磷酸化 LTB4 受体来反向调节 LTB4 诱导的高分子量糖蛋白分泌。因此,RvE1 和 RvD1 受体都通过使用β肾上腺素能受体激酶磷酸化 LTB4 受体来直接抑制 LTB4。RvE1 受体反向调节 LTB4 诱导的[Ca]和分泌增加,而 RvD1 受体仅反向调节 LTB4 诱导的[Ca]增加。