Please use this identifier to cite or link to this item:
|Title:||Gene and Protein Expressions in Human Cord Blood Cells After Exposure to Acrylonitrile|
|Authors:||DIODOVICH Cristina; MALERBA Ilaria; FERRARIO DANIELE; BOWE GERARD; BIANCHI Marco Giorgio; ACQUATI Francesco; TARAMELLI Roberto; PARENT-MASSIN Dominique; GRIBALDO LAURA|
|Citation:||JOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGY vol. 19 no. 4 p. 204-212|
|Publisher:||JOHN WILEY & SONS INC|
|Type:||Articles in Journals|
|Abstract:||Acrylonitrile is a very high volume industrial chemical used primarily in the manufacture of plastics and rubber, which displays a pronounced acute toxicity and may be carcinogenic. The damage to the hematopoietic function by acrylonitrile may result from interference with cytokine production and cytokine receptor binding. Our present data show that acrylonitrile modulates the expression of some genes implicated in cell differentiation, cell-cycle progression, and clonogenic potential of human cord blood cells.Amacroarray hybridization analysis showed that expression of the CXCR4, MCP-1, and MRP8 genes was modified by acrylonitrile exposure. Moreover, the acrylonitrile cell target seems to be the myeloid compartment, as assessed by a CFU-GM assay. In particular, the downregulation of CXCR4, MCP1, and MRP8 can be responsible for the observed reduction of cell proliferation and clonogenic capability of CFU-GM precursors. A Western blot assay showed an acrylonitriledependent induction of Bax, while Bcl-2 expression changed only after 48 h of chemical exposure. Bax was overexpressed in respect to Bcl-2, and this fact can be responsible for the induction in cell death after 24 h of treatment. C-fos and c-jun were also downregulated after 24 h and 6 h of treatment, respectively.|
|JRC Institute:||Institute for Health and Consumer Protection|
Files in This Item:
There are no files associated with this item.
Items in repository are protected by copyright, with all rights reserved, unless otherwise indicated.