Journal of Nutrition LabDiet, Your World of Nutritional Answers

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Purchase Article
Right arrow View Shopping Cart
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Stipanuk, M. H.
Right arrow Articles by Coloso, R. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Stipanuk, M. H.
Right arrow Articles by Coloso, R. M.
© 2006 The American Society for Nutrition J. Nutr. 136:1652S-1659S, June 2006


Supplement: 5th Amino Acid Assessment Workshop: Session I

Mammalian Cysteine Metabolism: New Insights into Regulation of Cysteine Metabolism1,2

Martha H. Stipanuk3, John E. Dominy, Jr., Jeong-In Lee and Relicardo M. Coloso

Division of Nutritional Sciences, Cornell University, Ithaca, NY

3 To whom correspondence should be addressed. E-mail: mhs6{at}cornell.edu.

The mammalian liver tightly regulates its free cysteine pool, and intracellular cysteine in rat liver is maintained between 20 and 100 nmol/g even when sulfur amino acid intakes are deficient or excessive. By keeping cysteine levels within a narrow range and by regulating the synthesis of glutathione, which serves as a reservoir of cysteine, the liver addresses both the need to have adequate cysteine to support normal metabolism and the need to keep cysteine levels below the threshold of toxicity. Cysteine catabolism is tightly regulated via regulation of cysteine dioxygenase (CDO) levels in the liver, with the turnover of CDO protein being dramatically decreased when intracellular cysteine levels increase. This occurs in response to changes in the intracellular cysteine concentration via changes in the rate of CDO ubiquitination and degradation. Glutathione synthesis also increases when intracellular cysteine levels increase as a result of increased saturation of glutamate-cysteine ligase (GCL) with cysteine, and this contributes to removal of excess cysteine. When cysteine levels drop, GCL activity increases, and the increased capacity for glutathione synthesis facilitates conservation of cysteine in the form of glutathione (although the absolute rate of glutathione synthesis still decreases because of the lack of substrate). This increase in GCL activity is dependent on up-regulation of expression of both the catalytic and modifier subunits of GCL, resulting in an increase in total catalytic subunit plus an increase in the catalytic efficiency of the enzyme. An important role of cysteine utilization for coenzyme A synthesis in maintaining cellular cysteine levels in some tissues, and a possible connection between the necessity of controlling cellular cysteine levels to regulate the rate of hydrogen sulfide production, have been suggested by recent literature and are areas that deserve further study.


KEY WORDS: • cysteine • cysteine dioxygenase • glutathione • glutamate-cysteine ligase • hypotaurine • taurine • coenzyme A • cysteamine • hydrogen sulfide




This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
G. D. Westrop, I. Georg, and G. H. Coombs
The Mercaptopyruvate Sulfurtransferase of Trichomonas vaginalis Links Cysteine Catabolism to the Production of Thioredoxin Persulfide
J. Biol. Chem., November 27, 2009; 284(48): 33485 - 33494.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
S. Verbruggen, J. Sy, W. E. Gordon, J. Hsu, M. Wu, S. Chacko, D. Zurakowski, D. Burrin, and L. Castillo
Ontogeny of methionine utilization and splanchnic uptake in critically ill children
Am J Physiol Endocrinol Metab, November 1, 2009; 297(5): E1046 - E1055.
[Abstract] [Full Text] [PDF]


Home page
J. Nutr.Home page
I. Ueki and M. H. Stipanuk
3T3-L1 Adipocytes and Rat Adipose Tissue Have a High Capacity for Taurine Synthesis by the Cysteine Dioxygenase/Cysteinesulfinate Decarboxylase and Cysteamine Dioxygenase Pathways
J. Nutr., February 1, 2009; 139(2): 207 - 214.
[Abstract] [Full Text] [PDF]


Home page
J. Nutr.Home page
G. Courtney-Martin, M. Rafii, L. J. Wykes, R. O. Ball, and P. B. Pencharz
Methionine-Adequate Cysteine-Free Diet Does Not Limit Erythrocyte Glutathione Synthesis in Young Healthy Adult Men
J. Nutr., November 1, 2008; 138(11): 2172 - 2178.
[Abstract] [Full Text] [PDF]


Home page
J. Nutr.Home page
R. N. Dilger and D. H. Baker
Excess Dietary L-Cysteine Causes Lethal Metabolic Acidosis in Chicks
J. Nutr., September 1, 2008; 138(9): 1628 - 1633.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
J. E. Dominy Jr., J. Hwang, S. Guo, L. L. Hirschberger, S. Zhang, and M. H. Stipanuk
Synthesis of Amino Acid Cofactor in Cysteine Dioxygenase Is Regulated by Substrate and Represents a Novel Post-translational Regulation of Activity
J. Biol. Chem., May 2, 2008; 283(18): 12188 - 12201.
[Abstract] [Full Text] [PDF]


Home page
Physiol. GenomicsHome page
J.-I. Lee, J. E. Dominy Jr., A. K. Sikalidis, L. L. Hirschberger, W. Wang, and M. H. Stipanuk
HepG2/C3A cells respond to cysteine deprivation by induction of the amino acid deprivation/integrated stress response pathway
Physiol Genomics, April 1, 2008; 33(2): 218 - 229.
[Abstract] [Full Text] [PDF]


Home page
J. Nutr.Home page
I. Ueki and M. H. Stipanuk
Enzymes of the Taurine Biosynthetic Pathway Are Expressed in Rat Mammary Gland
J. Nutr., August 1, 2007; 137(8): 1887 - 1894.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
J. E. Dominy Jr., J. Hwang, and M. H. Stipanuk
Overexpression of cysteine dioxygenase reduces intracellular cysteine and glutathione pools in HepG2/C3A cells
Am J Physiol Endocrinol Metab, July 1, 2007; 293(1): E62 - E69.
[Abstract] [Full Text] [PDF]


Home page
J. Nutr.Home page
G. K. Grimble
Adverse Gastrointestinal Effects of Arginine and Related Amino Acids
J. Nutr., June 1, 2007; 137(6): 1693S - 1701S.
[Abstract] [Full Text] [PDF]


Home page
CarcinogenesisHome page
S. K. Niture, C. S. Velu, Q. R. Smith, G.J. Bhat, and K. S. Srivenugopal
Increased expression of the MGMT repair protein mediated by cysteine prodrugs and chemopreventative natural products in human lymphocytes and tumor cell lines
Carcinogenesis, February 1, 2007; 28(2): 378 - 389.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Gastrointest. Liver Physiol.Home page
S. M. Bailey, G. Robinson, A. Pinner, L. Chamlee, E. Ulasova, M. Pompilius, G. P. Page, D. Chhieng, N. Jhala, A. Landar, et al.
S-adenosylmethionine prevents chronic alcohol-induced mitochondrial dysfunction in the rat liver
Am J Physiol Gastrointest Liver Physiol, November 1, 2006; 291(5): G857 - G867.
[Abstract] [Full Text] [PDF]


Home page
J. Nutr.Home page
R. O. Ball, G. Courtney-Martin, and P. B. Pencharz
The In Vivo Sparing of Methionine by Cysteine in Sulfur Amino Acid Requirements in Animal Models and Adult Humans
J. Nutr., June 1, 2006; 136(6): 1682S - 1693S.
[Abstract] [Full Text] [PDF]




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
Copyright © 2006 by American Society for Nutrition