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新生儿发育过程中的免疫和代谢变化重新编程了肝脏的身份和功能。

Immune and metabolic shifts during neonatal development reprogram liver identity and function.

机构信息

Center for Gastrointestinal Biology, Departamento de Morfologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais 31270-901, Brazil.

Departamento de Morfologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais 31270-901, Brazil.

出版信息

J Hepatol. 2018 Dec;69(6):1294-1307. doi: 10.1016/j.jhep.2018.08.018. Epub 2018 Aug 30.

Abstract

BACKGROUND & AIMS: The liver is the main hematopoietic site in embryos, becoming a crucial organ in both immunity and metabolism in adults. However, how the liver adapts both the immune system and enzymatic profile to challenges in the postnatal period remains elusive. We aimed to identify the mechanisms underlying this adaptation.

METHODS

We analyzed liver samples from mice on day 0 after birth until adulthood. Human biopsies from newborns and adults were also examined. Liver immune cells were phenotyped using mass cytometry (CyTOF) and expression of several genes belonging to immune and metabolic pathways were measured. Mortality rate, bacteremia and hepatic bacterial retention after E. coli challenge were analyzed using intravital and in vitro approaches. In a set of experiments, mice were prematurely weaned and the impact on gene expression of metabolic pathways was evaluated.

RESULTS

Human and mouse newborns have a sharply different hepatic cellular composition and arrangement compared to adults. We also found that myeloid cells and immature B cells primarily compose the neonatal hepatic immune system. Although neonatal mice were more susceptible to infections, a rapid evolution to an efficient immune response was observed. Concomitantly, newborns displayed a reduction of several macronutrient metabolic functions and the normal expression level of enzymes belonging to lipid and carbohydrate metabolism was reached around the weaning period. Interestingly, early weaning profoundly disturbed the expression of several hepatic metabolic pathways, providing novel insights into how dietary schemes affect the metabolic maturation of the liver.

CONCLUSION

In newborns, the immune and metabolic profiles of the liver are dramatically different to those of the adult liver, which can be explained by the differences in the liver cell repertoire and phenotype. Also, dietary and antigen cues may be crucial to guide liver development during the postnatal phase.

LAY SUMMARY

Newborns face major challenges in the extra-uterine life. In fact, organs need to modify their cellular composition and gene expression profile in order to adapt to changes in both microbiota and diet throughout life. The liver is interposed between the gastrointestinal system and the systemic circulation, being the destination of all macronutrients and microbial products from the gut. Therefore, it is expected that delicately balanced mechanisms govern the transformation of a neonatal liver to a key organ in adults.

摘要

背景与目的

肝脏是胚胎期的主要造血部位,在成人期成为免疫和代谢的关键器官。然而,肝脏如何适应出生后时期的免疫系统和酶谱挑战仍不清楚。我们旨在确定这种适应的机制。

方法

我们分析了出生后第 0 天至成年期的小鼠肝脏样本。还检查了新生儿和成年人的人类活检。使用质谱流式细胞术(CyTOF)对肝脏免疫细胞进行表型分析,并测量了属于免疫和代谢途径的几个基因的表达。使用体内和体外方法分析大肠杆菌挑战后的死亡率、菌血症和肝脏细菌保留率。在一组实验中,小鼠被过早断奶,并评估了对代谢途径基因表达的影响。

结果

与成人相比,人类和新生小鼠的肝脏细胞组成和排列有明显不同。我们还发现,髓样细胞和未成熟 B 细胞主要构成新生儿的肝脏免疫系统。尽管新生小鼠更容易感染,但观察到快速进化为有效的免疫反应。同时,新生儿表现出几种宏量营养素代谢功能的减少,并且脂质和碳水化合物代谢所属酶的正常表达水平在断奶期左右达到。有趣的是,早期断奶会严重扰乱肝脏的几种代谢途径的表达,为饮食方案如何影响肝脏的代谢成熟提供了新的见解。

结论

在新生儿中,肝脏的免疫和代谢特征与成人肝脏明显不同,这可以用肝脏细胞库和表型的差异来解释。此外,饮食和抗原线索可能对指导出生后阶段的肝脏发育至关重要。

概要

新生儿在子宫外生活中面临重大挑战。事实上,为了适应一生中微生物群和饮食的变化,器官需要改变其细胞组成和基因表达谱。肝脏位于胃肠道系统和全身循环之间,是来自肠道的所有宏量营养素和微生物产物的目的地。因此,预计微妙平衡的机制控制着从新生儿肝脏到成人关键器官的转变。

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