Department of Cancer Biology and Genetics, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08544, USA; Department of Chemistry, Princeton University, Princeton, NJ 08544, USA.
Cell Metab. 2018 Feb 6;27(2):428-438.e5. doi: 10.1016/j.cmet.2017.12.006. Epub 2018 Jan 11.
When mammalian cells are deprived of glutamine, exogenous asparagine rescues cell survival and growth. Here we report that this rescue results from use of asparagine in protein synthesis. All mammalian cell lines tested lacked cytosolic asparaginase activity and could not utilize asparagine to produce other amino acids or biosynthetic intermediates. Instead, most glutamine-deprived cell lines are capable of sufficient glutamine synthesis to maintain essential amino acid uptake and production of glutamine-dependent biosynthetic precursors, with the exception of asparagine. While experimental introduction of cytosolic asparaginase could enhance the synthesis of glutamine and increase tricarboxylic acid cycle anaplerosis and the synthesis of nucleotide precursors, cytosolic asparaginase suppressed the growth and survival of cells in glutamine-depleted medium in vitro and severely compromised the in vivo growth of tumor xenografts. These results suggest that the lack of asparaginase activity represents an evolutionary adaptation to allow mammalian cells to survive pathophysiologic variations in extracellular glutamine.
当哺乳动物细胞被剥夺谷氨酰胺时,外源性天冬酰胺可挽救细胞存活和生长。在这里,我们报告说,这种挽救是由于天冬酰胺在蛋白质合成中的使用。我们测试的所有哺乳动物细胞系均缺乏细胞质天冬酰胺酶活性,无法利用天冬酰胺来产生其他氨基酸或生物合成中间体。相反,大多数谷氨酰胺剥夺的细胞系能够进行足够的谷氨酰胺合成,以维持必需氨基酸的摄取和谷氨酰胺依赖性生物合成前体的产生,除了天冬酰胺。虽然实验引入细胞质天冬酰胺酶可以增强谷氨酰胺的合成,并增加三羧酸循环的碳同化作用和核苷酸前体的合成,但细胞质天冬酰胺酶在体外抑制了谷氨酰胺剥夺培养基中细胞的生长和存活,并严重损害了肿瘤异种移植物的体内生长。这些结果表明,缺乏天冬酰胺酶活性代表了一种进化适应,使哺乳动物细胞能够在细胞外谷氨酰胺的病理生理变化中存活。