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Benzo( a)pyrene, but not 2,3,7,8-tetrachlorodibenzo- p-dioxin, alters cell adhesion proteins in human uterine RL95-2 cells
This study compared the effects of benzo( a)pyrene (BaP) and 2,3,7,8-tetrachlorodibenzo- p-dioxin (TCDD), two aryl hydrocarbon receptor agonists, on cell attachment and adherens junction proteins in RL95-2 human uterine endometrial cells. Exposure to 10 μ M BaP significantly decreased cell attachmen...
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Published in: | Biochemical and biophysical research communications 2002-05, Vol.294 (1), p.101-107 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | This study compared the effects of benzo(
a)pyrene (BaP) and 2,3,7,8-tetrachlorodibenzo-
p-dioxin (TCDD), two aryl hydrocarbon receptor agonists, on cell attachment and adherens junction proteins in RL95-2 human uterine endometrial cells. Exposure to
10
μ
M BaP significantly decreased cell attachment to Matrigel, whereas 10
nM TCDD had no effect. Immunocytochemistry and Western immunoblot analysis showed that BaP, but not TCDD, produced a marked loss of plasma membrane epidermal growth factor receptor (EGF-R) localized along intercellular boundaries. BaP-treated cells exhibited significant decreases in β-catenin and cadherin protein levels, while vinculin levels remained unchanged relative to control. In contrast, TCDD treatment had no effect on the levels of β-catenin, cadherin, or vinculin. Further studies using the fluorescein labeled peptide phalloidin showed the presence of continuous subcortical actin filaments in control cells, whereas BaP-treated cells had subcortical actin aggregates. Thus, in contrast to TCDD, BaP produces a loss of cell attachment involving decreased localization of molecules important for cell–cell interactions in RL95-2 cells. |
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ISSN: | 0006-291X 1090-2104 |
DOI: | 10.1016/S0006-291X(02)00437-0 |