‘In vivo’ effects of Bisphenol A in Mytilus hemocytes: modulation of kinase-mediated signalling pathways

• Published in: Aquatic toxicology 2005-01, Vol.71 (1), p.73-84
• Main Authors: Canesi, Laura, Betti, Michele, Lorusso, Lucia Cecilia, Ciacci, Caterina, Gallo, Gabriella
• Format: Article
• Language: English
• Subjects: Activating Transcription Factor 1; Animal, plant and microbial ecology; Animals; Applied ecology; Benzhydryl Compounds; Biological and medical sciences; Bivalvia - drug effects; Bivalvia - metabolism; Blotting, Western; CREB; DNA-Binding Proteins - metabolism; Ecotoxicology, biological effects of pollution; Electrophoresis, Polyacrylamide Gel; Endocrine disrupters; Estrogens, Non-Steroidal - toxicity; Extracellular Signal-Regulated MAP Kinases - metabolism; Fundamental and applied biological sciences. Psychology; General aspects; Hemocytes; Hemocytes - drug effects; Hemocytes - enzymology; Hemocytes - metabolism; Immunity; Kinase-mediated cell signalling; Lysosomal membrane stability; Lysosomes - drug effects; Lysosomes - metabolism; MAP Kinase Signaling System - drug effects; MAPK; Marine; Milk Proteins - metabolism; Mytilus galloprovincialis; p38 Mitogen-Activated Protein Kinases - metabolism; Phenols - toxicity; Phosphorylation - drug effects; STAT; STAT3 Transcription Factor; STAT5 Transcription Factor; Trans-Activators - metabolism; Transcription Factors - metabolism
• ISSN: 0166-445X; 1879-1514
• DOI: 10.1016/j.aquatox.2004.10.011

Endocrine disrupting chemicals (EDCs) include a variety of natural and synthetic estrogens, as well as estrogen-mimicking chemicals. We have previously shown that in the hemocytes of the mussel Mytilus galloprovincialis Lam. both natural and environmental estrogens in vitro can rapidly affect the phosphorylation state of components of tyrosine kinase-mediated cell signalling, in particular of mitogen activated protein kinases (MAPKs) and signal transducers and activators of transcription (STAT), that are involved in mediating the hemocyte immune response. These effects were consistent with the hypothesis that ‘alternative’ modes of estrogen action involving kinase-mediated pathways similar to those described in mammalian systems are also present in invertebrate cells. This possibility was investigated in vivo with Bisphenol A (BPA): mussels were injected with BPA and hemocytes sampled at 6, 12, and 24 h post-injection. The results show that BPA (25 nM nominal concentration in the hemolymph) lead to a significant lysosomal membrane destabilisation at all times post-injection, indicating BPA-induced stress conditions in the hemocytes, whereas lower concentrations were ineffective. BPA induced significant changes in the phosphorylation state of MAPK and STAT members, as evaluated by SDS-PAGE and WB of hemocyte protein extracts with specific antibodies, although to a different degree at different exposure times. In particular, BPA induced a dramatic decrease in phosphorylation of the stress-activated p38 MAPK, whose activation is crucial in mediating the bactericidal activity. Moreover, BPA decreased the phosphorylation of a CREB-like transcription factor (cAMP-responsive element binding protein). The results demonstrate that BPA can affect kinase-mediated cell signalling in mussel hemocytes also in vivo, and suggest that EDCs may affect gene expression in mussel cells through modulation of the activity of transcription factors secondary to cytosolic kinase cascades. Overall, these data address the importance of investigating full range responses to EDCs in ecologically relevant marine invertebrate species.