Pesticide induced marrow toxicity and effects on marrow cell population and on hematopoietic stroma

• Published in: Experimental and toxicologic pathology : official journal of the Gesellschaft für Toxikologische Pathologie Vol. 65; no. 3; pp. 287 - 295
• Main Authors: Chatterjee, Sumanta, Basak, Pratima, Chaklader, Malay, Das, Prosun, Pereira, Jacintha Archana, Chaudhuri, Samaresh, Law, Sujata
• Format: Journal Article
• Language: English
• Published: Germany Elsevier GmbH 01.03.2013
• Subjects: animal models; Animals; apoptosis; Apoptosis - drug effects; bone marrow; Bone Marrow - drug effects; Bone Marrow - immunology; Bone Marrow - pathology; Bone marrow cell apoptosis; bone marrow cells; breathing; caspase-3; Cell Culture Techniques; cell proliferation; CFU; Chlorpyrifos - toxicity; Colony-Forming Units Assay; fibroblasts; Flow Cytometry; hematopoiesis; Hematopoietic Stem Cells - drug effects; Hematopoietic Stem Cells - immunology; Hematopoietic Stem Cells - pathology; humans; Insecticides - toxicity; interleukin-2; interleukin-3; interleukin-5; Mice; pesticidal properties; Pesticide; pesticides; Pyrethrins - toxicity; receptors; Receptors, Interleukin-2 - biosynthesis; Receptors, Interleukin-3 - biosynthesis; Receptors, Interleukin-5 - biosynthesis; stem cells; stromal cells; stromal microenvironment; Toxicity; Bone marrow cell apoptosis; CFU; Pesticide; Toxicity; stromal microenvironment
• ISSN: 0940-2993; 1618-1433
• DOI: 10.1016/j.etp.2011.09.002

Long term inhalation of toxic pesticides used for the domestic and industrial purposes have been shown to cause moderate to severe hematotoxicity and increased incidence of several marrow degenerative diseases, specifically hypoplastic bone marrow failure condition in humans. The progression of pesticide induced hematotoxicity and the exact underlying mechanisms of toxicity that play major role in limiting normal hematopoiesis are not quite well explained. In this present study, we have developed an animal model of hypoplastic bone marrow failure following pesticide exposure to show the deleterious effects of toxic pesticides on mouse hematopoietic system. Here we have presented the results of studying long-term marrow explant culture, IL-2, IL-3 and IL-5 receptors expression profile, fibroblast colony forming unit (CFU-F), hematopoietic progenitor cell colony formation and caspase-3 expression by the bone marrow cells. We have also identified the expression levels of several extracellular apoptosis markers (CD95/Fas) and intracellular apoptosis inducer proteins (pASK1, pJNK, caspase-3 and cleaved caspase-3) in the bone marrow cells of pesticide exposed mice. The long-term marrow explant culture demonstrated the impairment in proliferation of the stromal cells/stromal fibroblasts in culture. Decreased IL-2, IL-3 and IL-5 receptors expression profile essentially hinted at the suppressed cytokine activity in the pesticide exposed marrow. CFU-F analysis showed the defect in functional maturation of the stromal fibroblasts. The decreased hematopoietic progenitor cell colony formation indicated the toxicity induced inhibition of cellular proliferation and functional maturation of hematopoietic stem/progenitor cells in pesticide exposed marrow. We have detected a sharp increase in the expression levels of both the extracellular Fas-antigen and intracellular apoptosis inducer proteins in the bone marrow cells of pesticide exposed mice that explained well, the apoptosis pathway involved following marrow toxicity. The decreased proliferation and functional maturation of marrow stromal cells and hematopoietic progenitors with subsequent increase in marrow cellular apoptosis following pesticide toxicity provided the base necessary for explaining the increased incidence of hypoplastic bone marrow failure in humans exposed to moderate to high concentrations of pesticides.