Reversal of hydroquinone-mediated suppression of T cell proliferation by transfection of the M2 subunit of ribonucleotide reductase

Qing Li, Jane Kasten-Jolly, Yun Yen, Brian M. Freed

Research output: Contribution to journalArticle

18 Citations (Scopus)

Abstract

Hydroquinone (HQ) is a benzene derivative that is found in large quantities in cigarette tar as a result of the pyrolysis of tobacco flavinoids. HQ is a potent inhibitor of T cell proliferation, causing an immediate and complete cessation of DNA synthesis in IL-2-dependent human T lymphoblasts and Jurkat T cells without loss of cell viability. Previous studies from our laboratory demonstrated that the antiproliferative effects of HQ could be partially reversed by the addition of deoxyribonucleosides, but not by the corresponding ribonucleosides, suggesting that HQ might inhibit ribonucleotide reductase. In the present study, the molecular mechanism behind this observation was further investigated. Jurkat T cells were stably transfected with a pMEP4 expression vector containing the gene for the M2 subunit of ribonucleotide reductase under transcriptional control of the human metallothionein IIA promoter. M2-transfected Jurkat T cells exhibited a greater than three-fold increase in resistance to HQ compared to untransfected cells or cells transfected with the M2 gene in the reverse orientation. HQ resistance was associated with an increased level of M2 protein detected by Western blot. These results suggest that the benzene derivative inhibits lymphocyte proliferation by inhibiting ribonucleotide reductase.

Original languageEnglish
Pages (from-to)154-157
Number of pages4
JournalToxicology and Applied Pharmacology
Volume150
Issue number1
DOIs
Publication statusPublished - Jan 1 1998
Externally publishedYes

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T-cells
Cell proliferation
Transfection
Cell Proliferation
T-Lymphocytes
Jurkat Cells
Benzene Derivatives
Ribonucleotide Reductases
Genes
Deoxyribonucleosides
Ribonucleosides
Lymphocytes
Tobacco
Metallothionein
Interleukin-2
hydroquinone
ribonucleotide reductase M2
Cell Survival
Pyrolysis
Western Blotting

ASJC Scopus subject areas

  • Toxicology
  • Pharmacology

Cite this

Reversal of hydroquinone-mediated suppression of T cell proliferation by transfection of the M2 subunit of ribonucleotide reductase. / Li, Qing; Kasten-Jolly, Jane; Yen, Yun; Freed, Brian M.

In: Toxicology and Applied Pharmacology, Vol. 150, No. 1, 01.01.1998, p. 154-157.

Research output: Contribution to journalArticle

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