Department of Pediatrics, Indiana University School of Medicine, Indiana University, Indianapolis, Indiana.
Department of Anatomy, Cell Biology & Physiology, Indiana University School of Medicine, Indianapolis, Indiana.
Am J Physiol Lung Cell Mol Physiol. 2021 Apr 1;320(4):L640-L659. doi: 10.1152/ajplung.00417.2020. Epub 2021 Jan 27.
During postnatal lung development, metabolic changes that coincide with stages of alveolar formation are poorly understood. Responding to developmental and environmental factors, metabolic changes can be rapidly and adaptively altered. The objective of the present study was to determine biological and technical determinants of metabolic changes during postnatal lung development. Over 118 metabolic features were identified by liquid chromatography with tandem mass spectrometry (LC-MS/MS, Sciex QTRAP 5500 Triple Quadrupole). Biological determinants of metabolic changes were the transition from the postnatal saccular to alveolar stages and exposure to 85% hyperoxia, an environmental insult. Technical determinants of metabolic identification were brevity and temperature of harvesting, both of which improved metabolic preservation within samples. Multivariate statistical analyses revealed the transition between stages of lung development as the period of major metabolic alteration. Of three distinctive groups that clustered by age, the saccular stage was identified by its enrichment of both glycolytic and fatty acid derivatives. The critical transition between stages of development were denoted by changes in amino acid derivatives. Of the amino acid derivatives that significantly changed, a majority were linked to metabolites of the one-carbon metabolic pathway. The enrichment of one-carbon metabolites was independent of age and environmental insult. Temperature was also found to significantly influence the metabolic levels within the postmortem sampled lung, which underscored the importance of methodology. Collectively, these data support not only distinctive stages of metabolic change but also highlight amino acid metabolism, in particular one-carbon metabolites as metabolic signatures of the early postnatal lung.
在出生后肺发育过程中,与肺泡形成阶段同时发生的代谢变化还知之甚少。代谢变化可以快速适应发育和环境因素的变化。本研究的目的是确定出生后肺发育过程中代谢变化的生物学和技术决定因素。通过液相色谱串联质谱(LC-MS/MS,Sciex QTRAP 5500 Triple Quadrupole)鉴定了超过 118 种代谢特征。代谢变化的生物学决定因素是从出生后的囊泡阶段到肺泡阶段的过渡以及暴露于 85%的高氧环境,这是一种环境刺激。代谢鉴定的技术决定因素是收获的短暂性和温度,这两者都能改善样品内的代谢保存。多变量统计分析显示,肺发育阶段的过渡是主要代谢改变的时期。在按年龄聚类的三个不同组中,囊泡阶段的特点是糖酵解和脂肪酸衍生物都很丰富。发育阶段之间的关键转变是由氨基酸衍生物的变化来表示的。在显著变化的氨基酸衍生物中,大多数与一碳代谢途径的代谢物有关。一碳代谢物的富集与年龄和环境刺激无关。温度也被发现显著影响死后取样肺内的代谢水平,这凸显了方法学的重要性。总的来说,这些数据不仅支持了代谢变化的独特阶段,而且还强调了氨基酸代谢,特别是一碳代谢物作为早期出生后肺的代谢特征。