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D. Melzer, P. Gates, N. J. Osborne, W. E. Henley, R. Cipelli, A. Young, C. Money, P. McCormack, P. Schofield, D. Mosedale, D. Grainger and T. S. Galloway, “Urinary Bisphenol a Concentration and Angiography-Defined Coronary Artery Stenosis,” PLoS ONE, Vol. 7, No. 8, 2012, Article ID: e43378. doi:10.1371/journal.pone.0043378

has been cited by the following article:

• TITLE: Impact of Bisphenol A (BPA) and Free Fatty Acids (FFA) on Th2 Cytokine Secretion from INS-1 Cells

  AUTHORS: Johan N. van Oppen, Eugen J. Verspohl

  KEYWORDS: Bisphenol A; Th2 Cytokines; INS-1 Cells

  JOURNAL NAME: Pharmacology & Pharmacy, Vol.4 No.5, August 23, 2013

  ABSTRACT: Bisphenol A (BPA) is used in huge amounts for many plastic products and is a hormone (estrogen) disrupting agent. BPA as well as FFAs may be deleterious for the immune system. The aim was to identify Th2 cytokines and some of their signal transduction mechanisms in INS-1 cells, an insulin secreting cell line. Screening using a proteome profile indicated an increase of IL-1, IL-2, IL-4, IL-6, IL-10, IL-13 and IL-17 by BPA. Also FFAs (in combination with LPS) were positive. In detailed quantitative measurements, these results were confirmedly indicating a complex array of pro-and anti-inflammatory potential. The interaction of BPA with 17β-estradiol was non-additive with respect to IL-4 and IL-6 release and additive with respect to FFA interaction indicating same and different mechanisms of action, respecttively. As signal transduction PI3K (Wortmannin-sensitive) and STAT-3/6 (Tofacitinib-sensitive) are involved in various effects, INS-1 cells release several cytokines due to BPA and FFA attack which may be involved in disturbance of glucose homoeostasis and type 1 diabetes.