Modulation of membrane lipid composition and homeostasis in salmon hepatocytes exposed to hypoxia and perfluorooctane sulfonamide, given singly or in combination
The relative importance of environmental hypoxia due to global climate change on organismal ability to adapt to chemical insult and/or mechanisms of these responses is not well understood. Therefore, we have studied the effects of combined exposure to perfluorooctane sulfonamide (PFOSA) and chemical...
Gespeichert in:
Hauptverfasser: | , , |
---|---|
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext bestellen |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | The relative importance of environmental hypoxia due to global climate change on organismal ability to adapt to chemical
insult and/or mechanisms of these responses is not well understood. Therefore, we have studied the effects of combined
exposure to perfluorooctane sulfonamide (PFOSA) and chemically induced hypoxia on membrane lipid profile and
homeostasis. Primary salmon hepatocytes were exposed to PFOSA at 0, 25 and 50 mM singly or in combination with either
cobalt chloride (CoCl2: 0 and 150 mM) or deferroxamine (DFO: 0 and 100 mM) for 24 and 48 h. CoCl2 and DFO were used to
induce cellular hypoxia because these two chemicals have been commonly used in animal experiments for this purpose and
have been shown to increase hypoxia-inducible factor 1-alpha (HIF-1a) and vascular endothelial growth factor (VEGF) levels.
Fatty acid (FA) profiles were determined by GC-MS, while gene expression patterns were determined by quantitative PCR.
Hypoxic condition was confirmed with time-related increases of HIF-1a mRNA levels in CoCl2 and DFO exposed cells. In
general, significant alterations of genes involved in lipid homeostasis were predominantly observed after 48 h exposure.
Gene expression analysis showed that biological responses related to peroxisome proliferation (peroxisome proliferatoractivated
receptors (PPARs) and acyl coenzyme A (ACOX)) and FA desaturation (D5- and D6-desaturases: FAD5 and FAD6,
respectively) and elongation (FAE) were elevated slightly by single exposure (i.e. either PFOSA, CoCl2 or DFO exposure
alone), and these responses were potentiated in combined exposure conditions. Principal component analysis (PCA)
showed a clustering of peroxisome proliferation responses at transcript levels and FA desaturation against membrane FAs
levels whose changes were explained by PFOSA and chemically induced hypoxia exposures. Overall, our data show that
most of the observed responses were stronger in combined stressor exposure conditions, compared to individual stressor
exposure. In general, our data show that hypoxia may, singly or in combination with PFOSA produce deleterious health,
physiological and developmental consequences through the alteration of membrane lipid profile in organisms. |
---|