Anaphase-promoting complex/cyclosome-Cdh1 coordinates glycolysis and glutaminolysis with transition to S phase in human T lymphocytes

被引:98
作者
Colombo, Sergio L. [1 ]
Palacios-Callender, Miriam [1 ]
Frakich, Nanci [1 ]
De Leon, Joel [1 ]
Schmitt, Christoph A. [1 ]
Boorn, Leanne [1 ]
Davis, Nicola [1 ]
Moncada, Salvador [1 ]
机构
[1] UCL, Wolfson Inst Biomed Res, London WC1E 6BT, England
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
cell cycle; glutaminase; 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase isoform 3; proliferation; GROWTH RATE; METABOLISM; CELLS; RAT; CULTURE; PROLIFERATION; GLUTAMINASE; APC/C-CDH1; PROTEIN; MITOSIS;
D O I
10.1073/pnas.1012362107
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cell proliferation is accompanied by an increase in the utilization of glucose and glutamine. The proliferative response is dependent on a decrease in the activity of the ubiquitin ligase anaphase-promoting complex/cyclosome (APC/C)-Cdh1 which controls G1-to- S-phase transition by targeting degradation motifs, notably the KEN box. This occurs not only in cell cycle proteins but also in the glycolysis-promoting enzyme 6-phosphofructo-2-kinase/fructose- 2,6-bisphosphatase isoform 3 (PFKFB3), as we have recently demonstrated in cells in culture. We now show that APC/C-Cdh1 controls the proliferative response of human T lymphocytes. Moreover, we have found that glutaminase 1 is a substrate for this ubiquitin ligase and appears at the same time as PFKFB3 in proliferating T lymphocytes. Glutaminase 1 is the first enzyme in glutaminolysis, which converts glutamine to lactate, yielding intermediates for cell proliferation. Thus APC/C-Cdh1 is responsible for the provision not only of glucose but also of glutamine and, as such, accounts for the critical step that links the cell cycle with the metabolic substrates essential for its progression.
引用
收藏
页码:18868 / 18873
页数:6
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