Induction of cystine and glutamate transport activity in human fibroblasts by diethyl maleate and other electrophilic agents

The transport activity for cystine and glutamate in cultured human diploid fibroblasts is enhanced in response to diethyl maleate treatment. The enhancement is time- and dose-related, with a lag of about 3 h, and maximum enhancement (approximately 3-fold increase in the rate of uptake) is attained a...

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Published in:The Journal of biological chemistry Vol. 259; no. 4; pp. 2435 - 2440
Main Author: Bannai, S
Format: Journal Article
Language:English
Published: Bethesda, MD Elsevier Inc 25-02-1984
American Society for Biochemistry and Molecular Biology
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Abstract The transport activity for cystine and glutamate in cultured human diploid fibroblasts is enhanced in response to diethyl maleate treatment. The enhancement is time- and dose-related, with a lag of about 3 h, and maximum enhancement (approximately 3-fold increase in the rate of uptake) is attained after 1 to 2 days of incubation of the cells with 0.1 mM diethyl maleate. The enhancement of the transport activity is accompanied by an increase in the Vmax and little change in the Km, and it requires RNA and protein synthesis. Other electrophilic agents, such as cyclohex-2-en-1-one, ethacrynic acid, 1,2-epoxy-3-(p-nitro-phenoxy)propane, and sulfobromophthalein, similarly enhance the transport activity. These electrophiles are known as agents that interact with glutathione. For example, diethyl maleate at high concentrations, i.e. 1 mM, depletes intracellular glutathione and injures the cells. However, at relatively low concentrations diethyl maleate and other electrophilic compounds do cause increases in the intracellular levels of glutathione which we attribute to the enhanced uptake of cystine. It is suggested that the transport system for cystine and glutamate is involved in a protective mechanism of cells against an electrophilic attack.
AbstractList The transport activity for cystine and glutamate in cultured human diploid fibroblasts is enhanced in response to diethyl maleate treatment. The enhancement is time- and dose-related, with a lag of about 3 h, and maximum enhancement (approximately 3-fold increase in the rate of uptake) is attained after 1 to 2 days of incubation of the cells with 0.1 mM diethyl maleate. The enhancement of the transport activity is accompanied by an increase in the Vmax and little change in the Km, and it requires RNA and protein synthesis. Other electrophilic agents, such as cyclohex-2-en-1-one, ethacrynic acid, 1,2-epoxy-3-(p-nitro-phenoxy)propane, and sulfobromophthalein, similarly enhance the transport activity. These electrophiles are known as agents that interact with glutathione. For example, diethyl maleate at high concentrations, i.e. 1 mM, depletes intracellular glutathione and injures the cells. However, at relatively low concentrations diethyl maleate and other electrophilic compounds do cause increases in the intracellular levels of glutathione which we attribute to the enhanced uptake of cystine. It is suggested that the transport system for cystine and glutamate is involved in a protective mechanism of cells against an electrophilic attack.
The transport activity for cystine and glutamate in cultured human diploid fibroblasts is enhanced in response to diethyl maleate treatment. The enhancement is time- and dose-related, with a lag of about 3 h, and maximum enhancement (approximately 3-fold increase in the rate of uptake) is attained after 1 to 2 days of incubation of the cells with 0.1 mM diethyl maleate. The enhancement of the transport activity is accompanied by an increase in the Vmax and little change in the Km, and it requires RNA and protein synthesis. Other electrophilic agents, such as cyclohex-2-en-1-one, ethacrynic acid, 1,2-epoxy-3-(p-nitro-phenoxy)propane, and sulfobromophthalein, similarly enhance the transport activity. These electrophiles are known as agents that interact with glutathione. For example, diethyl maleate at high concentrations, i.e. 1 mM, depletes intracellular glutathione and injures the cells. However, at relatively low concentrations diethyl maleate and other electrophilic compounds do cause increases in the intracellular levels of glutathione which we attribute to the enhanced uptake of cystine. It is suggested that the transport system for cystine and glutamate is involved in a protective mechanism of cells against an electrophilic attack.
Author Bannai, S
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Cites_doi 10.1111/j.1432-1033.1982.tb06512.x
10.1016/S0021-9258(17)40447-9
10.1016/0005-2736(72)90097-1
10.1016/S0021-9258(19)69588-8
10.1002/jcp.1041120216
10.1016/S0021-9258(17)43372-2
10.4049/jimmunol.127.6.2257
10.1016/0003-2697(69)90064-5
10.1016/S0021-9258(19)83829-2
10.1016/S0065-230X(08)60848-9
10.1042/bj1040095
10.1016/S0021-9258(19)85901-X
10.1016/0006-2952(70)90075-4
10.1016/0167-4889(82)90017-9
10.1016/S0021-9258(19)69273-2
10.1016/0006-291X(77)90623-4
10.1172/JCI110285
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Issue 4
Keywords Human
Cell culture
Glutamic acid
Membrane transport
Aminoacid
Lung
Activation
Fibroblast
Cystine
Language English
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References Heaton, Gelehrter (bib5) 1977; 252
Tietze (bib13) 1969; 27
Bannai, Kitamura (bib2) 1980; 255
Christensen (bib1) 1979; 49
Bannai, Kitamura (bib7) 1982; 721
Brodie, Potter, Reed (bib11) 1982; 123
Gazzola, Franchi, Saibene, Ronchi, Guidotti (bib4) 1972; 266
Boyland, Chasseaud (bib8) 1967; 104
Bannai, Tsukeda, Okumura (bib12) 1977; 74
Takada, Bannai (bib18) 1984; 259
Boyland, Chasseaud (bib10) 1970; 19
Gazzola, Dall'Asta, Guidotti (bib6) 1981; 256
Wedner, Simchowitz, Stenson, Fischman (bib14) 1981; 68
Bannai, Ishii (bib16) 1982; 112
Bannai, Kitamura (bib3) 1981; 256
Makowske, Christensen (bib17) 1982; 257
Chasseaud (bib9) 1979; 29
Fischman, Udey, Kurtz, Wedner (bib15) 1981; 127
Takada (10.1016/S0021-9258(17)43371-0_bib18) 1984; 259
Bannai (10.1016/S0021-9258(17)43371-0_bib3) 1981; 256
Gazzola (10.1016/S0021-9258(17)43371-0_bib6) 1981; 256
Chasseaud (10.1016/S0021-9258(17)43371-0_bib9) 1979; 29
Boyland (10.1016/S0021-9258(17)43371-0_bib10) 1970; 19
Heaton (10.1016/S0021-9258(17)43371-0_bib5) 1977; 252
Tietze (10.1016/S0021-9258(17)43371-0_bib13) 1969; 27
Christensen (10.1016/S0021-9258(17)43371-0_bib1) 1979; 49
Makowske (10.1016/S0021-9258(17)43371-0_bib17) 1982; 257
Wedner (10.1016/S0021-9258(17)43371-0_bib14) 1981; 68
Bannai (10.1016/S0021-9258(17)43371-0_bib16) 1982; 112
Brodie (10.1016/S0021-9258(17)43371-0_bib11) 1982; 123
Bannai (10.1016/S0021-9258(17)43371-0_bib7) 1982; 721
Gazzola (10.1016/S0021-9258(17)43371-0_bib4) 1972; 266
Boyland (10.1016/S0021-9258(17)43371-0_bib8) 1967; 104
Bannai (10.1016/S0021-9258(17)43371-0_bib12) 1977; 74
Bannai (10.1016/S0021-9258(17)43371-0_bib2) 1980; 255
Fischman (10.1016/S0021-9258(17)43371-0_bib15) 1981; 127
References_xml – volume: 74
  start-page: 1582
  year: 1977
  end-page: 1588
  ident: bib12
  publication-title: Biochem. Biophys. Res. Commun.
  contributor:
    fullname: Okumura
– volume: 256
  start-page: 3191
  year: 1981
  end-page: 3198
  ident: bib6
  publication-title: J. Biol. Chem.
  contributor:
    fullname: Guidotti
– volume: 112
  start-page: 265
  year: 1982
  end-page: 272
  ident: bib16
  publication-title: J. Cell. Physiol.
  contributor:
    fullname: Ishii
– volume: 29
  start-page: 175
  year: 1979
  end-page: 274
  ident: bib9
  publication-title: Adv. Cancer Res.
  contributor:
    fullname: Chasseaud
– volume: 123
  start-page: 159
  year: 1982
  end-page: 164
  ident: bib11
  publication-title: Eur. J. Biochem.
  contributor:
    fullname: Reed
– volume: 27
  start-page: 502
  year: 1969
  end-page: 522
  ident: bib13
  publication-title: Anal. Biochem.
  contributor:
    fullname: Tietze
– volume: 259
  start-page: 2441
  year: 1984
  end-page: 2445
  ident: bib18
  publication-title: J. Biol. Chem.
  contributor:
    fullname: Bannai
– volume: 721
  start-page: 1
  year: 1982
  end-page: 10
  ident: bib7
  publication-title: Biochim. Biophys. Acta
  contributor:
    fullname: Kitamura
– volume: 256
  start-page: 5770
  year: 1981
  end-page: 5772
  ident: bib3
  publication-title: J. Biol. Chem.
  contributor:
    fullname: Kitamura
– volume: 252
  start-page: 2900
  year: 1977
  end-page: 2907
  ident: bib5
  publication-title: J. Biol. Chem.
  contributor:
    fullname: Gelehrter
– volume: 49
  start-page: 41
  year: 1979
  end-page: 101
  ident: bib1
  publication-title: Adv. Enzymol.
  contributor:
    fullname: Christensen
– volume: 266
  start-page: 407
  year: 1972
  end-page: 421
  ident: bib4
  publication-title: Biochim. Biophys. Acta
  contributor:
    fullname: Guidotti
– volume: 104
  start-page: 95
  year: 1967
  end-page: 102
  ident: bib8
  publication-title: Biochem. J.
  contributor:
    fullname: Chasseaud
– volume: 255
  start-page: 2372
  year: 1980
  end-page: 2376
  ident: bib2
  publication-title: J. Biol. Chem.
  contributor:
    fullname: Kitamura
– volume: 68
  start-page: 535
  year: 1981
  end-page: 543
  ident: bib14
  publication-title: J. Clin. Invest.
  contributor:
    fullname: Fischman
– volume: 127
  start-page: 2257
  year: 1981
  end-page: 2262
  ident: bib15
  publication-title: J. Immunol.
  contributor:
    fullname: Wedner
– volume: 19
  start-page: 1528
  year: 1970
  end-page: 1533
  ident: bib10
  publication-title: Biochem. Pharmacol.
  contributor:
    fullname: Chasseaud
– volume: 257
  start-page: 5663
  year: 1982
  end-page: 5670
  ident: bib17
  publication-title: J. Biol. Chem.
  contributor:
    fullname: Christensen
– volume: 123
  start-page: 159
  year: 1982
  ident: 10.1016/S0021-9258(17)43371-0_bib11
  publication-title: Eur. J. Biochem.
  doi: 10.1111/j.1432-1033.1982.tb06512.x
  contributor:
    fullname: Brodie
– volume: 252
  start-page: 2900
  year: 1977
  ident: 10.1016/S0021-9258(17)43371-0_bib5
  publication-title: J. Biol. Chem.
  doi: 10.1016/S0021-9258(17)40447-9
  contributor:
    fullname: Heaton
– volume: 266
  start-page: 407
  year: 1972
  ident: 10.1016/S0021-9258(17)43371-0_bib4
  publication-title: Biochim. Biophys. Acta
  doi: 10.1016/0005-2736(72)90097-1
  contributor:
    fullname: Gazzola
– volume: 256
  start-page: 3191
  year: 1981
  ident: 10.1016/S0021-9258(17)43371-0_bib6
  publication-title: J. Biol. Chem.
  doi: 10.1016/S0021-9258(19)69588-8
  contributor:
    fullname: Gazzola
– volume: 112
  start-page: 265
  year: 1982
  ident: 10.1016/S0021-9258(17)43371-0_bib16
  publication-title: J. Cell. Physiol.
  doi: 10.1002/jcp.1041120216
  contributor:
    fullname: Bannai
– volume: 259
  start-page: 2441
  year: 1984
  ident: 10.1016/S0021-9258(17)43371-0_bib18
  publication-title: J. Biol. Chem.
  doi: 10.1016/S0021-9258(17)43372-2
  contributor:
    fullname: Takada
– volume: 127
  start-page: 2257
  year: 1981
  ident: 10.1016/S0021-9258(17)43371-0_bib15
  publication-title: J. Immunol.
  doi: 10.4049/jimmunol.127.6.2257
  contributor:
    fullname: Fischman
– volume: 27
  start-page: 502
  year: 1969
  ident: 10.1016/S0021-9258(17)43371-0_bib13
  publication-title: Anal. Biochem.
  doi: 10.1016/0003-2697(69)90064-5
  contributor:
    fullname: Tietze
– volume: 257
  start-page: 5663
  year: 1982
  ident: 10.1016/S0021-9258(17)43371-0_bib17
  publication-title: J. Biol. Chem.
  doi: 10.1016/S0021-9258(19)83829-2
  contributor:
    fullname: Makowske
– volume: 29
  start-page: 175
  year: 1979
  ident: 10.1016/S0021-9258(17)43371-0_bib9
  publication-title: Adv. Cancer Res.
  doi: 10.1016/S0065-230X(08)60848-9
  contributor:
    fullname: Chasseaud
– volume: 104
  start-page: 95
  year: 1967
  ident: 10.1016/S0021-9258(17)43371-0_bib8
  publication-title: Biochem. J.
  doi: 10.1042/bj1040095
  contributor:
    fullname: Boyland
– volume: 49
  start-page: 41
  year: 1979
  ident: 10.1016/S0021-9258(17)43371-0_bib1
  publication-title: Adv. Enzymol.
  contributor:
    fullname: Christensen
– volume: 255
  start-page: 2372
  year: 1980
  ident: 10.1016/S0021-9258(17)43371-0_bib2
  publication-title: J. Biol. Chem.
  doi: 10.1016/S0021-9258(19)85901-X
  contributor:
    fullname: Bannai
– volume: 19
  start-page: 1528
  year: 1970
  ident: 10.1016/S0021-9258(17)43371-0_bib10
  publication-title: Biochem. Pharmacol.
  doi: 10.1016/0006-2952(70)90075-4
  contributor:
    fullname: Boyland
– volume: 721
  start-page: 1
  year: 1982
  ident: 10.1016/S0021-9258(17)43371-0_bib7
  publication-title: Biochim. Biophys. Acta
  doi: 10.1016/0167-4889(82)90017-9
  contributor:
    fullname: Bannai
– volume: 256
  start-page: 5770
  year: 1981
  ident: 10.1016/S0021-9258(17)43371-0_bib3
  publication-title: J. Biol. Chem.
  doi: 10.1016/S0021-9258(19)69273-2
  contributor:
    fullname: Bannai
– volume: 74
  start-page: 1582
  year: 1977
  ident: 10.1016/S0021-9258(17)43371-0_bib12
  publication-title: Biochem. Biophys. Res. Commun.
  doi: 10.1016/0006-291X(77)90623-4
  contributor:
    fullname: Bannai
– volume: 68
  start-page: 535
  year: 1981
  ident: 10.1016/S0021-9258(17)43371-0_bib14
  publication-title: J. Clin. Invest.
  doi: 10.1172/JCI110285
  contributor:
    fullname: Wedner
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Snippet The transport activity for cystine and glutamate in cultured human diploid fibroblasts is enhanced in response to diethyl maleate treatment. The enhancement is...
The transport activity for cystine and glutamate in cultured human diploid fibroblasts is enhanced in response to diethyl maleate treatment. The enhancement is...
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StartPage 2435
SubjectTerms Biological and medical sciences
Biological Transport - drug effects
Cell Line
Cell physiology
Cystine - metabolism
Female
Fibroblasts - drug effects
Fibroblasts - metabolism
Fundamental and applied biological sciences. Psychology
Glutamates - metabolism
Glutamic Acid
Humans
Kinetics
Lung - embryology
Maleates - pharmacology
Membrane and intracellular transports
Molecular and cellular biology
Pregnancy
Structure-Activity Relationship
Title Induction of cystine and glutamate transport activity in human fibroblasts by diethyl maleate and other electrophilic agents
URI https://dx.doi.org/10.1016/S0021-9258(17)43371-0
http://www.jbc.org/content/259/4/2435.abstract
https://www.ncbi.nlm.nih.gov/pubmed/6142042
https://search.proquest.com/docview/80963843
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