Blizard Institute, Queen Mary, University of London, London, UK.
Department of Cellular Pathology, Imperial College, London, UK.
J Pathol. 2020 Sep;252(1):41-52. doi: 10.1002/path.5481. Epub 2020 Jul 23.
The severity of sterile inflammation, as seen in acute pancreatitis, is determined by damage-sensing receptors, signalling cascades and cytokine production. Stat2 is a type I interferon signalling mediator that also has interferon-independent roles in murine lipopolysaccharide-induced NF-κB-mediated sepsis. However, its role in sterile inflammation is unknown. We hypothesised that Stat2 determines the severity of non-infective inflammation in the pancreas. Wild type (WT) and Stat2 mice were injected i.p. with caerulein or l-arginine. Specific cytokine-blocking antibodies were used in some experiments. Pancreata and blood were harvested 1 and 24 h after the final dose of caerulein and up to 96 h post l-arginine. Whole-tissue phosphoproteomic changes were assessed using label-free mass spectrometry. Tissue-specific Stat2 effects were studied in WT/Stat2 bone marrow chimera and using Cre-lox recombination to delete Stat2 in pancreatic and duodenal homeobox 1 (Pdx1)-expressing cells. Stat2 mice were protected from caerulein- and l-arginine-induced pancreatitis. Protection was independent of type I interferon signalling. Stat2 mice had lower cytokine levels, including TNF-α and IL-10, and reduced NF-κB nuclear localisation in pancreatic tissue compared with WT. Inhibition of TNF-α improved (inhibition of IL-10 worsened) caerulein-induced pancreatitis in WT but not Stat2 mice. Phosphoproteomics showed downregulation of MAPK mediators but accumulation of Ser412-phosphorylated Tak1. Stat2 deletion in Pdx1-expressing acinar cells (Stat2 ) reduced pancreatic TNF-α expression, but not histological injury or serum amylase. WT/Stat2 bone marrow chimera mice were protected from pancreatitis irrespective of host or recipient genotype. Stat2 loss results in disrupted signalling in pancreatitis, upstream of NF-κB in non-acinar and/or bone marrow-derived cells. © 2020 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.
无菌性炎症的严重程度,如急性胰腺炎中所见,由损伤感应受体、信号级联和细胞因子产生决定。Stat2 是一种 I 型干扰素信号转导介质,在小鼠脂多糖诱导的 NF-κB 介导的脓毒症中也具有干扰素非依赖性作用。然而,其在无菌性炎症中的作用尚不清楚。我们假设 Stat2 决定了胰腺中非感染性炎症的严重程度。野生型 (WT) 和 Stat2 小鼠经腹腔注射 caerulein 或 l-精氨酸。在一些实验中使用了特定的细胞因子阻断抗体。在最后一次 caerulein 给药后 1 和 24 小时以及 l-精氨酸给药后长达 96 小时收获胰腺和血液。使用无标记质谱法评估全组织磷酸化蛋白质组变化。在 WT/Stat2 骨髓嵌合体中研究组织特异性 Stat2 作用,并使用 Cre-lox 重组在胰腺和十二指肠同源盒 1 (Pdx1) 表达细胞中删除 Stat2。Stat2 小鼠免受 caerulein 和 l-精氨酸诱导的胰腺炎的影响。保护作用独立于 I 型干扰素信号转导。与 WT 相比,Stat2 小鼠的胰腺组织中细胞因子水平(包括 TNF-α 和 IL-10)较低,NF-κB 核定位减少。TNF-α 抑制改善(IL-10 抑制恶化)WT 但不改善 Stat2 小鼠的 caerulein 诱导的胰腺炎。磷酸蛋白质组学显示 MAPK 介质下调,但 Ser412 磷酸化 Tak1 积累。在 Pdx1 表达的腺泡细胞中删除 Stat2 (Stat2 )减少了胰腺 TNF-α 的表达,但不影响组织学损伤或血清淀粉酶。WT/Stat2 骨髓嵌合体小鼠无论宿主还是受者基因型如何均能免受胰腺炎的影响。Stat2 缺失导致胰腺炎信号传导中断,上游是在非腺泡细胞和/或骨髓来源细胞中 NF-κB。