Department of Pediatrics, RWTH Aachen University, Aachen, Germany.
Department of Medicine, RWTH Aachen University, Aachen, Germany.
Nat Commun. 2019 Apr 11;10(1):1685. doi: 10.1038/s41467-019-09359-8.
Neonatal sepsis is characterized by hyperinflammation causing enhanced morbidity and mortality compared to adults. This suggests differences in the response towards invading threats. Here we investigate activated cord blood macrophages (CBMΦ) in comparison to adult macrophages (PBMΦ), indicating incomplete interferon gamma (IFN-γ) and interleukin 10 (IL-10)-induced activation of CBMΦ. CBMΦ show reduced expression of phagocytosis receptors and cytokine expression in addition to altered energy metabolism. In particular, IFN-γ as well as IL-10-activated CBMΦ completely fail to increase glycolysis and furthermore show reduced activation of the mTOR pathway, which is important for survival in sepsis. MTOR inhibition by rapamycin equalizes cytokine production in CBMΦ and PBMΦ. Finally, incubation of PBMΦ with cord blood serum or S100A8/A9, which is highly expressed in neonates, suppresses mTOR activation, prevents glycolysis and the expression of an PBMΦ phenotype. Thus, a metabolic alteration is apparent in CBMΦ, which might be dependent on S100A8/A9 expression.
新生儿败血症的特征是过度炎症反应,与成人相比,其发病率和死亡率更高。这表明了机体对入侵威胁的反应存在差异。在此,我们研究了与成人巨噬细胞(PBMΦ)相比的脐带血激活巨噬细胞(CBMΦ),表明 CBMΦ 的干扰素γ(IFN-γ)和白细胞介素 10(IL-10)诱导激活不完全。CBMΦ 除了能量代谢改变外,还表现出吞噬作用受体和细胞因子表达减少。特别是,IFN-γ和 IL-10 激活的 CBMΦ 完全不能增加糖酵解,并且表现出 mTOR 通路的激活减少,mTOR 通路对于败血症中的存活很重要。雷帕霉素抑制 mTOR 可使 CBMΦ 和 PBMΦ 的细胞因子产生均等化。最后,用富含于新生儿的脐带血清或 S100A8/A9 孵育 PBMΦ,可抑制 mTOR 激活,阻止糖酵解和 PBMΦ 表型的表达。因此,CBMΦ 中存在明显的代谢改变,这可能依赖于 S100A8/A9 的表达。