Ammonium is a key determinant on the dietary restriction of yeast chronological aging in culture medium

被引:16
作者
Santos, Julia [1 ,2 ]
Leitao-Correia, Fernanda [3 ]
Sousa, Matria Joao [3 ]
Leao, Cecilia [1 ,2 ]
机构
[1] Univ Minho, Sch Hlth Sci, Life & Hlth Sci Res Inst ICVS, Braga, Portugal
[2] ICVS 3Bs PT Govt Associate Lab, Braga, Portugal
[3] Univ Minho, Dept Biol, Mol & Environm Biol Ctr CBMA, Braga, Portugal
关键词
Ammonium; lifespan; dietary restriction; amino acid restriction; yeast; DNA-REPLICATION STRESS; LIFE-SPAN; SACCHAROMYCES-CEREVISIAE; PROTEIN-KINASE; CONTROLS TORC1; LONGEVITY; EXTENDS; HOMEOSTASIS; SUPEROXIDE; AUTOPHAGY;
D O I
10.18632/oncotarget.2989
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
New evidences have recently emerged from studies in yeast and in higher eukaryotes showing the importance of nutrient balance in dietary regimes and its effects on longevity regulation. We have previously shown that manipulation of ammonium concentration in the culture and/or aging medium can drastically affect chronological lifespan (CLS) of Saccharomyces cerevisiae, especially in amino acid restricted cells. Here we describe that the CLS shortening under amino acid restriction can be completely reverted by removing ammonium from the culture medium. Furthermore, the absence of ammonium, and of any rich nitrogen source, was so effective in extending CLS that no beneficial effect could be observed by further imposing calorie restriction conditions. When present in the culture medium, ammonium impaired the consumption of the auxotrophy-complementing amino acids and caused in an improper cell cycle arrest of the culture. TOR1 deletion reverted ammonium effects both in amino acid restricted and non-restricted cultures, whereas, Ras2p and Sch9p seem to have only a milder effect in the mediation of ammonium toxicity under amino acid restriction and no effect on non-restricted cultures. Our studies highlight ammonium as a key effector in the nutritional equilibrium between rich and essential nitrogen sources and glucose required for longevity promotion.
引用
收藏
页码:6511 / 6523
页数:13
相关论文
共 51 条
[11]   Induction of autophagic flux by amino acid deprivation is distinct from nitrogen starvation-induced macroautophagy [J].
Ecker, Nitai ;
Mor, Angelica ;
Journo, Dikla ;
Abeliovich, Hagai .
AUTOPHAGY, 2010, 6 (07) :879-890
[12]   Sir2 blocks extreme life-span extension [J].
Fabrizio, P ;
Gattazzo, C ;
Battistella, L ;
Wei, M ;
Cheng, C ;
McGrew, K ;
Longo, VD .
CELL, 2005, 123 (04) :655-667
[13]   Superoxide is a mediator of an altruistic aging program in Saccharomyces cerevisiae [J].
Fabrizio, P ;
Battistella, L ;
Vardavas, R ;
Gattazzo, C ;
Liou, LL ;
Diaspro, A ;
Dossen, JW ;
Gralla, EB ;
Longo, VD .
JOURNAL OF CELL BIOLOGY, 2004, 166 (07) :1055-1067
[14]   The chronological life span of Saccharomyces cerevisiae [J].
Fabrizio, P ;
Longo, VD .
AGING CELL, 2003, 2 (02) :73-81
[15]   Extending Healthy Life Span-From Yeast to Humans [J].
Fontana, Luigi ;
Partridge, Linda ;
Longo, Valter D. .
SCIENCE, 2010, 328 (5976) :321-326
[16]  
Fortuna M, 2001, CURR PROTOC CYTOM
[17]   Amino acid sensing in dietary-restriction-mediated longevity: roles of signal-transducing kinases GCN2 and TOR [J].
Gallinetti, Jordan ;
Harputlugil, Eylul ;
Mitchell, James R. .
BIOCHEMICAL JOURNAL, 2013, 449 :1-10
[18]   Low auxotrophy-complementing amino acid concentrations reduce yeast chronological life span [J].
Gomes, Pedro ;
Sampaio-Marques, Belem ;
Ludovico, Paula ;
Rodrigues, Fernando ;
Leao, Cecilia .
MECHANISMS OF AGEING AND DEVELOPMENT, 2007, 128 (5-6) :383-391
[19]   Amino-acid imbalance explains extension of lifespan by dietary restriction in Drosophila [J].
Grandison, Richard C. ;
Piper, Matthew D. W. ;
Partridge, Linda .
NATURE, 2009, 462 (7276) :1061-U121
[20]  
Jiang JC, 2000, FASEB J, V14, P2135