Immunopharmacology Laboratory, Department of Biochemistry and Immunology, Instituto de Ciências Biológicas, UFMG, Belo Horizonte, Brazil; Signaling in Inflammation Laboratory, Department of Clinical and Toxicological Analysis, Faculdade de Farmácia, UFMG, Belo Horizonte, Brazil; Pulmonary and Critical Care Medicine Division, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA..
Immunopharmacology Laboratory, Department of Biochemistry and Immunology, Instituto de Ciências Biológicas, UFMG, Belo Horizonte, Brazil; Signaling in Inflammation Laboratory, Department of Clinical and Toxicological Analysis, Faculdade de Farmácia, UFMG, Belo Horizonte, Brazil.
Pharmacol Res. 2020 Sep;159:105030. doi: 10.1016/j.phrs.2020.105030. Epub 2020 Jun 17.
A complex intracellular signaling governs different cellular responses in inflammation. Extracellular stimuli are sensed, amplified, and transduced through a dynamic cellular network of messengers converting the first signal into a proper response: production of specific mediators, cell activation, survival, or death. Several overlapping pathways are coordinated to ensure specific and timely induction of inflammation to neutralize potential harms to the tissue. Ideally, the inflammatory response must be controlled and self-limited. Resolution of inflammation is an active process that culminates with termination of inflammation and restoration of tissue homeostasis. Comparably to the onset of inflammation, resolution responses are triggered by coordinated intracellular signaling pathways that transduce the message to the nucleus. However, the key messengers and pathways involved in signaling transduction for resolution are still poorly understood in comparison to the inflammatory network. cAMP has long been recognized as an inducer of anti-inflammatory responses and cAMP-dependent pathways have been extensively exploited pharmacologically to treat inflammatory diseases. Recently, cAMP has been pointed out as coordinator of key steps of resolution of inflammation. Here, we summarize the evidence for the role of cAMP at inducing important features of resolution of inflammation.
复杂的细胞内信号转导控制着炎症中的不同细胞反应。细胞外刺激通过信使的动态细胞网络被感知、放大和转导,将第一信号转化为适当的反应:产生特定的介质、细胞激活、存活或死亡。为了确保炎症的特异性和及时性,以中和组织潜在的伤害,几个重叠的途径被协调在一起。理想情况下,炎症反应必须得到控制并自我限制。炎症的消退是一个主动的过程,以炎症的终止和组织内稳态的恢复为终点。与炎症的发生相比,消退反应是由协调的细胞内信号通路触发的,这些信号通路将信号转导到细胞核。然而,与炎症网络相比,参与消退信号转导的关键信使和途径仍知之甚少。cAMP 长期以来一直被认为是抗炎反应的诱导剂,cAMP 依赖性途径已被广泛用于治疗炎症性疾病的药理学研究。最近,cAMP 被指出是炎症消退过程中关键步骤的协调者。在这里,我们总结了 cAMP 在诱导炎症消退的重要特征方面的作用的证据。