Department of Burn and Plastic Surgery, Nanjing First Hospital, Nanjing Medical University, Nanjing, PR China.
Department of Burn and Plastic Surgery, Nanjing First Hospital, Nanjing Medical University, Nanjing, PR China.
Biochem Biophys Res Commun. 2021 Mar 26;546:138-144. doi: 10.1016/j.bbrc.2021.01.110. Epub 2021 Feb 11.
Hepatic injury is common in patients who suffer from severe burns plus delayed resuscitation (B + DR). Stimulator of interferon genes (STING) is primarily expressed in Kupffer cells (KCs). We demonstrated that B + DR caused hepatic injury and oxidative stress. Reactive oxygen species (ROS) damage mitochondrial membranes in hepatocytes, leading to the release of mitochondrial DNA (mtDNA) into the hepatocyte cytosol and the circulation. The damaged hepatocytes then activate the mtDNA/STING pathway in KCs and trigger KCs polarization towards pro-inflammatory phenotype. SS-31 is a strong antioxidant that specifically concentrates in the inner mitochondrial membrane. SS-31 prevented hepatic injury by neutralizing ROS, inhibiting the release of mtDNA, protecting hepatocyte mitochondria, suppressing the activation of the mtDNA/STING pathway and inhibiting KCs polarization into pro-inflammatory phenotype.
肝损伤在遭受严重烧伤加延迟复苏(B+DR)的患者中很常见。干扰素基因刺激物(STING)主要在枯否细胞(KCs)中表达。我们证明 B+DR 可导致肝损伤和氧化应激。活性氧(ROS)破坏肝细胞中的线粒体膜,导致线粒体 DNA(mtDNA)释放到肝细胞胞质溶胶和循环中。受损的肝细胞随后激活 KCs 中的 mtDNA/STING 途径,并触发 KCs 向促炎表型极化。SS-31 是一种强抗氧化剂,专门在 线粒体 内 膜 中浓缩。SS-31 通过中和 ROS、抑制 mtDNA 的释放、保护肝细胞线粒体、抑制 mtDNA/STING 途径的激活和抑制 KCs 向促炎表型极化来防止肝损伤。