Hoogduijn_2006_Toxicol.Sci_94_342

Reference

Title : The effects of anticholinergic insecticides on human mesenchymal stem cells - Hoogduijn_2006_Toxicol.Sci_94_342
Author(s) : Hoogduijn MJ , Rakonczay Z , Genever PG
Ref : Toxicol Sci , 94 :342 , 2006
Abstract :

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.

PubMedSearch : Hoogduijn_2006_Toxicol.Sci_94_342
PubMedID: 16960032

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Citations formats

Hoogduijn MJ, Rakonczay Z, Genever PG (2006)
The effects of anticholinergic insecticides on human mesenchymal stem cells
Toxicol Sci 94 :342

Hoogduijn MJ, Rakonczay Z, Genever PG (2006)
Toxicol Sci 94 :342