The effects of anticholinergic insecticides on human mesenchymal stem cells

被引:37
作者
Hoogduijn, Martin J.
Rakonczay, Zoltan
Genever, Paul G. [1 ]
机构
[1] Univ York, Dept Biol, Biomed Tissue Res Grp, York YO10 5YW, N Yorkshire, England
[2] Univ Szeged, Dept Oral Biol, Szeged, Hungary
[3] Univ Szeged, Dept Psychiat, Albert Szent Gyorgyi Ctr Med & Pharmaceut Sci, Fac Med, H-3000 Szeged CA, Hungary
关键词
acetylcholine; acetylcholinesterase; carbofuran; chlorpyrifos; mesenchymal stem cell; osteogenesis;
D O I
10.1093/toxsci/kfl101
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 [卫生毒理学];
摘要
Mesenchymal stem cells (MSCs) are located primarily in the bone marrow and are characterized by their capacity to differentiate into mesenchymal lineages such as bone, fat, and cartilage in response to appropriate signals. Several signaling mechanisms act to control MSC survival, proliferation, and differentiation, and failure or disruption of these signaling pathways can lead to degenerative disease or neoplasia. Organophosphate (OP) and carbamate pesticides, which are used in large amounts in agriculture to control insects, are designed to disrupt acetylcholine signaling by inhibiting the enzyme acetylcholinesterase (AChE). Effects of OP and carbamate pesticides on the human central nervous system have been well documented. However, AChE is broadly distributed, and the effects of anticholinergic insecticides on nonnervous tissue have received little attention. In the present study we found that human MSCs express AChE, which makes these cells potential targets for AChE inhibiting agents. We therefore examined the effects of an OP pesticide, chlorpyrifos, and a carbamate, carbofuran, on MSC characteristics. It was found that micromolar concentrations of these anticholinergic insecticides had no effect on MSC survival or proliferation but limited MSC differentiation capacity by inhibiting osteogenic differentiation. These results demonstrate that exposure to micromolar concentrations of OP and carbamate pesticides may affect tissue turnover and pathophysiology by interfering with MSC regulation.
引用
收藏
页码:342 / 350
页数:9
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