ToxSci Advance Access published online on February 13, 2009
Toxicological Sciences, doi:10.1093/toxsci/kfp025
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Bisphenol A disrupts Notch signaling by inhibiting gamma-secretase activity and causes eye dysplasia of Xenopus laevis
* Nanobiotechnology Research Center and Department of Bioscience, School of Science and Technology, Kwansei Gakuin University, 2-1 Gakuen, Sanda 669-1337, Japan
Corresponding author : Susumu Imaoka, Ph.D. Department of Bioscience, School of Science and Technology, Kwansei Gakuin University, 2-1 Gakuen, Sanda 669-1337, Japan, E-mail: imaoka{at}kwansei.ac.jp, Tel/Fax: +81-79-565-7673
Received September 26, 2008; revision received January 30, 2009; accepted February 2, 2009
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Abstract |
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Bisphenol A (BPA) is being recognized as an endocrine-disrupting chemical (EDC). Recently, several reports indicated that BPA affects the central nervous system (CNS) during embryonic development. However, the molecular mechanism of BPA in the CNS is not well known. Here, we show that BPA affected Notch signaling by inhibiting the activity of the Notch intracellular domain (NICD) cleavage-related enzyme, gamma-secretase (
-secretase), at the neurula stage of the Xenopus laevis. BPA caused various morphologic aberrations including scoliosis, eye dysplasia and loss of pigments in the Xenopus laevis tadpole. These abnormalities were seen whenever BPA was used at the neurula stage. In addition, the expression levels of several marker mRNAs at the neurula stage were investigated by RT-PCR, and we found that the mRNAs expression of ectodermal marker, Pax6, CNS marker, Sox2, and neural crest marker, FoxD3, were decreased by treatment with BPA. These genes contribute to the neural differentiation at the neurula stage, and also the downstream factors of Notch signaling. Injection of NICD but not a Notch ligand, delta 1, rescued the abnormalities caused by BPA. We subsequently assayed the inhibition of the activities of NICD cleavage-related enzymes, tumor necrosis factor alpha converting enzyme (TACE) and -secretase, by BPA and found that BPA inhibited the -secretase activity. Furthermore, we expressed presenilin, a main component of -secretase, in E. coli and found the direct binding of BPA with presenilin. These results suggest that BPA affected the neural differentiation by inhibiting -secretase activity, leading to neurodevelopmental abnormalities.
Key Words: Bisphenol A; Notch signaling; Xenopus laevis embryo; neurula.
Present address: Department of Lifescience, Faculty of Science, Rikkyo University, 3-34-1 Nishi-Ikebukuro. Toshima-ku, Tokyo 171-8501 Japan