Literature DB >> 2609342

Macrophage regulation of myelopoiesis is altered by exposure to the benzene metabolite hydroquinone.

D J Thomas1, M J Reasor, D Wierda.   

Abstract

Hydroquinone, a myelotoxic metabolite of benzene, decreases the ability of murine bone marrow stromal cells to support myelopoiesis in vitro. Bone marrow stroma consists of macrophages and fibroblastoid stromal cells that participate coordinately in regulating myelopoiesis. The goal of this study was to determine if macrophage or fibroblastoid cell function is more sensitive to the myelotoxic actions of hydroquinone. To address this question, we developed purified populations of macrophages and fibroblastoid stromal cells and treated each population with hydroquinone. These cells were reconstituted together with nontreated cells of the opposite type and assayed for their ability to support the formation of granulocyte and macrophage colonies in an agar overlay. Reconstituted cultures containing hydroquinone-treated macrophages supported fewer colonies than did corresponding cultures containing untreated macrophages. Reconstituted cultures containing hydroquinone-treated fibroblastoid stromal cells were not affected. Moreover, hydroquinone reduced detectable interleukin-1 activity in purified macrophage cultures stimulated with lipopolysaccharide. These results indicate that hydroquinone selectively interferes with macrophage function possibly, in part, via alteration of macrophage interleukin-1 secretion.

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Year:  1989        PMID: 2609342     DOI: 10.1016/0041-008x(89)90249-4

Source DB:  PubMed          Journal:  Toxicol Appl Pharmacol        ISSN: 0041-008X            Impact factor:   4.219


  10 in total

1.  Evidence for strain-specific differences in benzene toxicity as a function of host target cell susceptibility.

Authors:  D J Neun; A Penn; C A Snyder
Journal:  Arch Toxicol       Date:  1992       Impact factor: 5.153

2.  Hematopoietic effects of benzene inhalation assessed by long-term bone marrow culture.

Authors:  N G Abraham
Journal:  Environ Health Perspect       Date:  1996-12       Impact factor: 9.031

3.  A morphological analysis of the short-term effects of benzene on the development of the hematological cells in the bone marrow of mice and the effects of interleukin-1 alpha on the process.

Authors:  R Niculescu; G F Kalf
Journal:  Arch Toxicol       Date:  1995       Impact factor: 5.153

4.  Role of nitric oxide in hematosuppression and benzene-induced toxicity.

Authors:  D L Laskin; D E Heck; C J Punjabi; J D Laskin
Journal:  Environ Health Perspect       Date:  1996-12       Impact factor: 9.031

5.  Cell-specific activation and detoxification of benzene metabolites in mouse and human bone marrow: identification of target cells and a potential role for modulation of apoptosis in benzene toxicity.

Authors:  D Ross; D Siegel; D G Schattenberg; X M Sun; J L Moran
Journal:  Environ Health Perspect       Date:  1996-12       Impact factor: 9.031

6.  p-Benzoquinone, a reactive metabolite of benzene, prevents the processing of pre-interleukins-1 alpha and -1 beta to active cytokines by inhibition of the processing enzymes, calpain, and interleukin-1 beta converting enzyme.

Authors:  G F Kalf; J F Renz; R Niculescu
Journal:  Environ Health Perspect       Date:  1996-12       Impact factor: 9.031

Review 7.  Analysis of target cell susceptibility as a basis for the development of a chemoprotective strategy against benzene-induced hematotoxicities.

Authors:  M A Trush; L E Twerdok; S J Rembish; H Zhu; Y Li
Journal:  Environ Health Perspect       Date:  1996-12       Impact factor: 9.031

8.  Case report: Hydroquinone and/or glutaraldehyde induced acute myeloid leukaemia?

Authors:  Vassilios Makropoulos; Evangelos C Alexopoulos
Journal:  J Occup Med Toxicol       Date:  2006-07-26       Impact factor: 2.646

9.  Metabolism of phenol and hydroquinone to reactive products by macrophage peroxidase or purified prostaglandin H synthase.

Authors:  M J Schlosser; R D Shurina; G F Kalf
Journal:  Environ Health Perspect       Date:  1989-07       Impact factor: 9.031

10.  Studies with 1,2-dithiole-3-thione as a chemoprotector of hydroquinone-induced toxicity to DBA/2-derived bone marrow stromal cells.

Authors:  L E Twerdok; S J Rembish; M A Trush
Journal:  Environ Health Perspect       Date:  1993-06       Impact factor: 9.031

  10 in total

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