Dipartimento di Scienze e Tecnologie Biologiche e Ambientali (Di.S.Te.B.A.), Università del Salento, Via Provinciale per Monteroni, Lecce, Italy.
Dipartimento di Scienze e Tecnologie Biologiche e Ambientali (Di.S.Te.B.A.), Università del Salento, Via Provinciale per Monteroni, Lecce, Italy.
Mol Cell Endocrinol. 2020 May 1;507:110771. doi: 10.1016/j.mce.2020.110771. Epub 2020 Feb 27.
Local mediator prostaglandins and bradykinin are involved in inflammation and pain. We explored bradykinin effects on prostaglandin E2 (PGE2) release from fibroblasts derived from human skeletal muscular biopsies. Bradykinin induced PGE release through bradykinin B2 receptors, since PGE release was blocked by the bradykinin B2 receptor selective antagonist FR173657 and B2 receptor agonist (Hyp)-bradykinin showed effects comparable to bradykinin. Consistently, bradykinin induced both mRNA cyclooxygenase 2 (COX-2) and protein. Bradykinin also induced ERK1/2 and p38 phosphorylation and provoked the translocation from the cytosol to the nucleus of p65/NF-kB. The release of PGE by bradykinin could be blocked inhibiting COX-2 and p65/NF-kB, ERK1/2 or p38 activation. Both ERK1/2 and p38 were upstream to NF-kB inasmuch siRNAs significantly blocked the p65/NF-kB activation induced by bradykinin. Thus, bradykinin, acting via B2 receptors, induced PGE release through ERK1/2 and p38-dependent pathways and consequent p65/NF-kB translocation to nucleus. p65/NF-kB induced COX-2 transcription. The release of PGE provide a possible explanation for the role of bradykinin in inflammatory diseases.
局部介质前列腺素和缓激肽参与炎症和疼痛。我们探讨了缓激肽对源自人骨骼肌活检的成纤维细胞中前列腺素 E2 (PGE2)释放的影响。缓激肽通过缓激肽 B2 受体诱导 PGE 释放,因为 PGE 释放被缓激肽 B2 受体选择性拮抗剂 FR173657 和缓激肽 B2 受体激动剂 (Hyp)-缓激肽阻断,并且显示出与缓激肽相当的作用。一致地,缓激肽诱导了 mRNA 环加氧酶 2 (COX-2)和蛋白。缓激肽还诱导了 ERK1/2 和 p38 的磷酸化,并促使 p65/NF-kB 从细胞质向核内易位。通过抑制 COX-2 和 p65/NF-kB、ERK1/2 或 p38 激活,可以阻断缓激肽引起的 PGE 释放。ERK1/2 和 p38 在 NF-kB 的上游,因为 siRNAs 显著阻断了缓激肽诱导的 p65/NF-kB 激活。因此,缓激肽通过 B2 受体作用,通过 ERK1/2 和 p38 依赖的途径诱导 PGE 释放,并导致 p65/NF-kB 易位到核内。p65/NF-kB 诱导 COX-2 转录。PGE 的释放为缓激肽在炎症性疾病中的作用提供了可能的解释。