Department of Biochemistry and Molecular Biology, College of Medicine, University of Florida, Gainesville, FL 32610, USA.
School of Biological Sciences, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA.
Nutrients. 2023 Apr 18;15(8):1938. doi: 10.3390/nu15081938.
The natural amino acid asparagine (Asn) is required by cells to sustain function and proliferation. Healthy cells can synthesize Asn through asparagine synthetase (ASNS) activity, whereas specific cancer and genetically diseased cells are forced to obtain asparagine from the extracellular environment. ASNS catalyzes the ATP-dependent synthesis of Asn from aspartate by consuming glutamine as a nitrogen source. Asparagine Synthetase Deficiency (ASNSD) is a disease that results from biallelic mutations in the ASNS gene and presents with congenital microcephaly, intractable seizures, and progressive brain atrophy. ASNSD often leads to premature death. Although clinical and cellular studies have reported that Asn deprivation contributes to the disease symptoms, the global metabolic effects of Asn deprivation on ASNSD-derived cells have not been studied. We analyzed two previously characterized cell culture models, lymphoblastoids and fibroblasts, each carrying unique ASNS mutations from families with ASNSD. Metabolomics analysis demonstrated that Asn deprivation in ASNS-deficient cells led to disruptions across a wide range of metabolites. Moreover, we observed significant decrements in TCA cycle intermediates and anaplerotic substrates in ASNS-deficient cells challenged with Asn deprivation. We have identified pantothenate, phenylalanine, and aspartate as possible biomarkers of Asn deprivation in normal and ASNSD-derived cells. This work implies the possibility of a novel ASNSD diagnostic via targeted biomarker analysis of a blood draw.
天然氨基酸天冬酰胺(Asn)是细胞维持功能和增殖所必需的。健康细胞可以通过天冬酰胺合成酶(ASNS)的活性合成 Asn,而特定的癌症和遗传性疾病细胞则被迫从细胞外环境中获取天冬酰胺。ASNS 通过消耗谷氨酰胺作为氮源,催化 ATP 依赖性的天冬氨酸与 Asn 的合成。天冬酰胺合成酶缺乏症(ASNSD)是一种由 ASNS 基因的双等位基因突变引起的疾病,表现为先天性小头畸形、难治性癫痫和进行性脑萎缩。ASNSD 常导致过早死亡。尽管临床和细胞研究报告指出,天冬酰胺剥夺会导致疾病症状,但天冬酰胺剥夺对 ASNSD 来源细胞的全局代谢影响尚未得到研究。我们分析了两种以前表征的细胞培养模型,即淋巴母细胞和成纤维细胞,它们各自携带来自 ASNSD 家族的独特 ASNS 突变。代谢组学分析表明,在 ASNS 缺陷细胞中天冬酰胺剥夺会导致广泛的代谢物紊乱。此外,我们观察到在天冬酰胺剥夺挑战下,ASNS 缺陷细胞中的 TCA 循环中间产物和补料合成底物显著减少。我们已经确定泛酸、苯丙氨酸和天冬氨酸是正常和 ASNSD 来源细胞中天冬酰胺剥夺的可能生物标志物。这项工作意味着通过对血液样本进行靶向生物标志物分析,可能会有新的 ASNSD 诊断方法。