The Ah receptor recognizes DNA binding sites for the B cell transcription factor, BSAP: a possible mechanism for dioxin-mediated alteration of CD19 gene expression in human B lymphocytes
- PMID: 7541987
- DOI: 10.1006/bbrc.1995.1931
The Ah receptor recognizes DNA binding sites for the B cell transcription factor, BSAP: a possible mechanism for dioxin-mediated alteration of CD19 gene expression in human B lymphocytes
Abstract
2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) inhibits murine and human B lymphocyte immunoglobulin production through an unknown mechanism. This study investigated the effect of TCDD on expression of the CD19 gene in a human B lymphocyte cell line. Northern blot analysis showed that TCDD treatment decreased steady state levels of CD19 mRNA by 67% in the IM-9 cell line. Using a gel mobility shift assay, we identified a DNA-binding complex in IM-9 nuclear extracts that by several criteria appears to be the Ah receptor. In addition, the Ah receptor complex recognized a DNA binding site for B cell lineage-specific activator protein (BSAP) in the promoter region of the human CD19 gene which is similar to the consensus Ah receptor DNA binding site. These results suggest that the AhR could interfere with BSAP-stimulated CD19 gene transcription by competition for a common DNA binding site.
Similar articles
-
Characterization of the aryl hydrocarbon receptor complex in human B lymphocytes: evidence for a distinct nuclear DNA-binding form.Arch Biochem Biophys. 1996 Dec 15;336(2):297-308. doi: 10.1006/abbi.1996.0561. Arch Biochem Biophys. 1996. PMID: 8954578
-
Aryl hydrocarbon receptor-dependent suppression by 2,3,7, 8-tetrachlorodibenzo-p-dioxin of IgM secretion in activated B cells.Mol Pharmacol. 1998 Apr;53(4):623-9. Mol Pharmacol. 1998. PMID: 9547351
-
The human estrogen receptor structural gene contains a DNA sequence that binds activated mouse and human Ah receptors: a possible mechanism of estrogen receptor regulation by 2,3,7,8-tetrachlorodibenzo-p-dioxin.Biochem Biophys Res Commun. 1993 Jun 30;193(3):956-62. doi: 10.1006/bbrc.1993.1718. Biochem Biophys Res Commun. 1993. PMID: 8391813
-
The role of BSAP (Pax-5) in B-cell development.Curr Opin Genet Dev. 1995 Oct;5(5):595-601. doi: 10.1016/0959-437x(95)80028-x. Curr Opin Genet Dev. 1995. PMID: 8664547 Review.
-
Induction of hepatic cytochrome P450 gene expression by 2,3,7,8-tetrachlorodibenzo-p-dioxin.Mol Biol Med. 1989 Apr;6(2):169-78. Mol Biol Med. 1989. PMID: 2693891 Review.
Cited by
-
Disruption of human plasma cell differentiation by an environmental polycyclic aromatic hydrocarbon: a mechanistic immunotoxicological study.Environ Health. 2010 Mar 24;9:15. doi: 10.1186/1476-069X-9-15. Environ Health. 2010. PMID: 20334656 Free PMC article.
-
Aryl Hydrocarbon Receptor Activation Suppresses EBF1 and PAX5 and Impairs Human B Lymphopoiesis.J Immunol. 2017 Nov 15;199(10):3504-3515. doi: 10.4049/jimmunol.1700289. Epub 2017 Oct 4. J Immunol. 2017. PMID: 28978690 Free PMC article.
-
2,3,7,8-tetrachlorodibenzo-p-dioxin induces transcriptional activity of the human polymorphic hs1,2 enhancer of the 3'Igh regulatory region.J Immunol. 2012 Apr 1;188(7):3294-306. doi: 10.4049/jimmunol.1101111. Epub 2012 Feb 22. J Immunol. 2012. PMID: 22357631 Free PMC article.
-
A single mid-gestation exposure to TCDD yields a postnatal autoimmune signature, differing by sex, in early geriatric C57BL/6 mice.Toxicology. 2011 Dec 18;290(2-3):156-68. doi: 10.1016/j.tox.2011.08.021. Epub 2011 Sep 6. Toxicology. 2011. PMID: 21925233 Free PMC article.
-
The long winding road toward understanding the molecular mechanisms for B-cell suppression by 2,3,7,8-tetrachlorodibenzo-p-dioxin.Toxicol Sci. 2011 Mar;120 Suppl 1(Suppl 1):S171-91. doi: 10.1093/toxsci/kfq324. Epub 2010 Oct 15. Toxicol Sci. 2011. PMID: 20952503 Free PMC article. Review.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources