Dimethyldithiocarbamate inhibits in vitro activation of primary human CD4 T lymphocytes (Q77114939)

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3 December 2019

title

Dimethyldithiocarbamate inhibits in vitro activation of primary human CD4 T lymphocytes (English)

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3 December 2019

author name string

D W Pyatt

1

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3 December 2019

J Gruntmeir

2

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3 December 2019

W S Stillman

3

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3 December 2019

R D Irons

4

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publication date

1 July 1998

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3 December 2019

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volume

128

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issue

2

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page(s)

83-90

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2-mercaptoethanol restores the ability of nuclear factor kappa B (NF kappa B) to bind DNA in nuclear extracts from interleukin 1-treated cells incubated with pyrollidine dithiocarbamate (PDTC). Evidence for oxidation of glutathione in the mechanism

3 December 2019

cites work

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Kappa B-specific DNA binding proteins: role in the regulation of human interleukin-2 gene expression

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Nonequivalent effects of PKC activation by PMA on murine CD4 and CD8 cell-surface expression

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Evaluation of the immunomodulatory potential of diethyl dithiocarbamate derivatives

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Dithiocarbamates Induce Apoptosis in Thymocytes by Raising the Intracellular Level of Redox-active Copper

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Dithiocarbamates and the redox regulation of cell death

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Tumor necrosis factor alpha and interleukin 1 stimulate the human immunodeficiency virus enhancer by activation of the nuclear factor kappa B

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Disparate effects of representative dithiocarbamates on selected immunological parameters in vivo and cell survival in vitro in female B6C3F1 mice

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Immunotoxicological characteristics of sodium methyldithiocarbamate

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Inorganic lead activates NF-kappa B in primary human CD4 T lymphocytes

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7 January 2021

Function and activation of the transcription factor NF-kappa B in the response to toxins and pathogens

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Dithiocarbamates as potent inhibitors of nuclear factor kappa B activation in intact cells

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Depletion of the mitochondrial electron transport abrogates the cytotoxic and gene-inductive effects of TNF.

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NF-kappa B: a lesson in family values

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Phospholipases and protein kinases during phagocyte activation

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10.1016/S0300-483X(98)00047-X

Identifiers

DOI

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3 December 2019

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