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NEW-TOOL TO INVESTIGATE TOXICOLOGICAL HAZARD DUE TO
ENDOCRINE DISRUPTORS IN MEDITERRANEAN CETACEANS
Department of Environmental Sciences, Siena University, Via Mattioli 4, 53100 Siena, Italy.
Mediterranean cetaceans, particularly odontocetes, accumulate high concentrations of
organochlorine contaminants (OCs) and are therefore exposed to high toxicological risk.
Some OCs are known to be endocrine disrupting compounds (EDCs). The hypothesis that
Mediterranean cetaceans (Stenella coeruleoalba, Delphinus delphis, Tursiops truncatus
) are subject to toxicological risk due to organochlorines and emerging
contaminants, such as polybrominated diphenyl ethers (PBDEs) with endocrine disrupting
capacity, was investigated using non-lethal “diagnostic” and “prognostic” methods. CYP1A1
activity induction (Benzo(a)pyrene monooxygenase) in skin biopsies was used as a
“diagnostic” indicator of exposure to organochlorines in odontocetes and mysticetes and in
different populations of Stenella coeruleoalba
. Marked differences in levels of OCs and
CYP1A1 activity were found between fin whales and odontocetes. Organochlorine levels and
CYP1A1 activity were significantly higher in the Stenella coeruleoalba
population of the
Mediterranean Whale Sanctuary than in those of two other study areas, suggesting that
cetaceans are exposed to high risk in this protected area.
Several questions remain still unanswered in ecotoxicological studies of Mediterranean
cetaceans. The need for new biomarkers for EDCs and for a “cell model” to explore the
different susceptibilities to several classes of ECDs, including emerging contaminants, led us
to culture fibroblasts of different cetacean species as a non-lethal new investigation tool
(“dolphins in test tubes”). As a new “prognostic” tool we explored interspecies and gender
susceptibility to OC-EDCs and PBDEs using qualitative and semi-quantitative evaluation of
target proteins, such as CYP1A1 and CYP 2B in cultured cetacean (Stenella coeruleoalba,
and Balaenoptera physalus
) fibroblasts, by western blot,
immunofluorescence technique and PCR real time. The information obtained in this pilot
experiment will be the basis for further applications and validation of these methodologies to
expolore different species and gender susceptibility of marine mammals to different mixtures
of endocrine disrupting xenobiotics including emerging contaminants.
: MEDITERRANEAN CETACEANS, ORGANOCHLORINE CONTAMINANTS;
BROMINATED FLAME RETARDANTS; ENDOCRINE DISRUPTING CHEMICALS; FIBROBLASTS
CELL CULTURE; IMMUNOFLUORESCENCE TECHNIQUE.
Mediterranean top predators, and particularly cetacean odontocetes, accumulate high
concentrations of organochlorine contaminants (OCs) and are therefore exposed to high
Some organochlorine compounds, now with worldwide distribution, are
known as endocrine disrupting chemicals (EDCs). Four types of organochlorine endocrine
disruptors are commonly found in Mediterranean cetaceans (Fossi et al., 2003): 1)
environmental estrogens, 2) environmental androgens, 3) anti-estrogens and 4) anti-
androgens. The relative estrogenic power of these chemicals, identified by in vitro
and in vivo
screening methods is rather weak (10 or less) compared with the reference power of 17-B-
estradiol or DES. However, the high levels of organochlorine compounds detected in
Mediterranean cetaceans, and consequently, the high levels of organochlorines with ED
Polybrominated diphenyl ethers (PBDEs) are a major family of brominated flame retardants,
and are lipophilic, persistent and toxic to fauna and humans (Alaee et al., 2003). There is
growing concern about accumulation of brominated organic compounds in the food chain.
The highest levels of PBDEs have been found in top marine predators.
Some general considerations on the potential hazard to these Mediterranean species can be
drawn from comparison of the levels of OC-EDCs commonly detected in Mediterranean
cetaceans and that of other cetacean species with known reproductive impairment. Several
examples suggest that exposure to OC insecticides and PCBs has affected endocrine function
and reproduction in marine mammals (Fossi & Marsili, 2003). Alarmingly, levels of PCBs
found in the subcutaneous blubber biopsies of Mediterranean free ranging odontocetes
sampled in the period 1992-1999 (striped dolphin (Stenella coeruleoalba
), bottlenose dolphin
) and common dolphin (Delphinus delphis
), mean value = 54587 ng/g
l.w.; 44924 ng/g l.w.; 25032 ng/g l.w. respectively) (Fossi et al., 2003) are similar to those
detected in the population of beluga whales of the St. Lawrence estuary, including a
hermaphrodite specimen (mean value = 78900 ng/g l.w.) (Muir et al., 1996); levels of PCBs
detected in the subcutaneous blubber biopsies of Mediterranean free ranging fin whales
) in the same period (mean value = 7331 ng/g l.w.) (Fossi & Marsili,
2003) are approximately 10 times higher than those found in the population of bowhead
whales (Balaena mysticetus
) characterised by pseudohermaphroditism and other reproductive
dysfunctions (mean value = 610 ng/g l.w.) (Hoeskra et al., 2003). These observations suggest
the potential risks associated with OC-EDC exposure in Mediterranean cetaceans.
All these considerations orientated our ecotoxicological research in Mediterranean cetaceans
towards field application of “diagnostic tools”, such as CYP1A1 induction (benzo(a)pyrene
monooxygenase activity) in skin biopsies and assay of OC levels in blubber, to assess the
exposure of species, populations and genders to OCs with endocrine disrupting capacity.
Moreover, the need to develop new biomarkers for EDCs and a cell model (“dolphins in test
tubes”) to explore different susceptibilities to several classes of EDCs, prompted us to culture
fibroblasts of different cetacean species. As “prognostic” tool we explored interspecies
bottlenose dolphin and fin whale) and gender susceptibilities to OC-EDCs
and PBDEs using qualitative and semi-quantitative assay of target proteins, such as CYP1A1
and CYP2B, in cultured cetacean fibroblasts by western blot and immunofluorescence
MATHERIALS AND METHODS
Subcutaneous tissues (skin and blubber) were obtained striped dolphin,
dolphin and fin whale from the western Ligurian Sea, between Corsica and the French-Italian
coast, and the Ionian Sea using an aluminium pole armed with biopsy tips or biopsy darts
launched with a crossbow (Barnett Wildcat II crossbow with a 150-pound test bow) (Fossi et al,
2003). Biopsy specimens were taken in the dorsal area near a dorsal fin and on the upper part of
the caudal peduncle. All material was immediately placed in liquid nitrogen or stored in cell
Cetacean gender was determined genetically according to Berube &
The small size of the biopsy samples (0.200 - 0.002 g) did not permit isolation
of microsomal fractions. CYP1A1 activity (BPMO) was detected in whole tissue. Since the
connective tissue was very tough, the epidermis was homogenized in 1.15% KCl buffer at pH 7.5
by thermal shock and separated by freezing in liquid N2 and pulverizing in a Potter apparatus
with ultrasound. BPMO activity was assessed using the incubation mixture proposed by Fossi et
al. (1992) incubating each sample (plus blanks) in a shaking bath for 2 h at 37°C. The activity was
expressed in arbitrary units of fluorescence (A.U.F./h/g tissue).
The samples of subcutaneous blubber (about 0.3 g) were freeze-dried and
extracted with n-hexane in a Soxhlet apparatus for analysis of chlorinated hydrocarbons. The
analytical method was High Resolution Capillary Gas Chromatography with a Perkin-Elmer
Series 8700 GC and a 63Ni ECD. Capillary gas-chromatography revealed op'- and pp'- isomers of
DDT and its derivatives DDD and DDE, and about 30 PCB congeners.
Fibroblasts cell culture.
The development of a non-invasive sampling method for obtaining
viable tissue samples for cell cultures from skin biopsies of free-ranging cetaceans was
described in Marsili et al. (2000). Successful cell cultures were obtained from striped dolphin,
bottlenose dolphin and fin whale. The first fibroblasts were observed after 7–21 days. Cultures
reached 90% confluence in 15–20 days, when they were trypsinized, washed and placed in
Falcon 50 and 125 flasks, after two and three trypsinizations respectively.
Fibroblast cultures (third generation) from striped dolphin (n=15),
bottlenose dolphin (n=2) and fin whale (n=3)
were subject to two different experimental
protocols for 48 h, using two classes of CYP450 inducers with EDCs potency. The first was a
mixture of Arochlor 1260, pp’DDT and pp’DDE in DMSO (0.05%) at three doses: 1 µg/ml, 5
µg/ml and 25 µg/ml, plus a DMSO (0.05%) control. The second was a mixture (BDE-MXE,
Wellington, Canada) containing 27 PBDEs, from mono- to deca-brominated, in nonane (0.01
µg/ml) at three doses: 0.1 µg/ml, 0.05 µg/ml and 0.01 µg/ml, plus a nonane (0.01 µg/ml)
For western blot analysis, fibroblast extracts were separated by SDS-PAGE
(10% polyacrylamide gels) and blotted into nitrocellulose sheets for 1 hour at a constant
voltage of 100 V. The membranes were saturated by incubating with blocking solution (2%
BSA in TTBS) for 1 hour at room temperature. Primary polyclonal goat IgG anti rabbit
antibodies CYP1A1/1A2 and CYP2B4 were purchased from Oxford Biomedical Research
(Michigan, USA). CYP1A1/1A2 and CYP 2B4 diluted 1:5000 and 1:1000 respectively in
TTBS-1% BSA, were allowed to incubate for 15 h at 4°C. Incubation with the BioRad anti-
goat HRP labelled secondary antibody (1:3000 final dilution) was performed for 1 hour at
room temperature and detection was carried out as outlined in the Amersham ECL kit booklet.
Semi-quantitative analysis was performed with Quantity One software (Bio-Rad).
We used immunofluorescence in fibroblast cultures for a qualitative
and semi-quantitative analysis of target proteins CYP1A1 and CYP2B. After a first reaction
with the primary antibodies for CYP1A1-1A2 and 2B4 (Oxford Biomedical Research),
cells were treated with the respective secondary antibodies marked with a fluorochrome.
RESULT AND DISCUSSION
In the last 15 years, in our Lab, we have mainly based ecotoxicological research in
Mediterranean cetaceans on “diagnostic tools”, namely CYP1A1 induction (benzo(a)pyrene
monooxygenase activity) in skin biopsies and quantification of OCs in blubber, to assess
different exposure of species, populations and genders to OCs in the Mediterranean Sea (Fossi
et al., 1992; Marsili et al., 1998; Fossi et al., 2003; Fossi & Marsili 2003). Several questions
With regard to species differences, we evaluated CYP1A1 (BPMO) activity in skin biopsies
of Mediterranean cetaceans (striped dolphin,
bottlenose dolphin, common dolphin and fin
whale) as a potential indicator of exposure to EDCs, such as OCs. In line with data in the
literature and results obtained in our lab before 1994 (Fossi et al., 1992; Marsili et al. 1998;
Fossi et al., 2003; Fossi & Marsili 2003), sharp differences in subcutaneous blubber levels of
all contaminants were found between fin whales (PCBs mean value=4.5 ng/g f.w; DDTs
mean value=5.3 f.w) and odontocete species (in striped dolphin, PCBs mean value=19.5 ng/g
f.w; DDTs mean value=20.1 f.w). The same was found for BPMO activity (fin whale, mean
value=140.5 U.A.F. g tissues/h; striped dolphin, mean value=270.2 U.A.F. g tissues/h). The
main explanation for these results is their different position in the food chain: odontocetes are
terminal consumers and fin whales are macroplanktophages.
Sex differences in CYP1A1 (BPMO) induction were also investigated. In striped dolphins a
linear correlation was found between op’DDT/BPMO and PCB153/BPMO (Fossi et al.,
2003). In the common dolphin five linear correlations with the BPMO activity were
identified: DDTs, pp’DDE, op’DDT, PCBs and PCB153. The main result in this species was
absence of induction of BPMO in females with increasing levels of contaminants. A similar
result was obtained in fin whales sampled in the Ligurian Sea from 1992 to 1995 (Marsili et
al., 1998). This difference in the inductive capacity of skin CYP1A1 (BPMO) between males
and females of this species was interesting but at that stage could not be explained.
With regard to population differences, organochlorine levels and CYP1A1 activity were
significantly greater in the striped dolphin population of the Mediterranean Whale Sanctuary
than in those of two other Mediterranean study areas, suggesting that cetaceans are exposed to
Several questions remain unanswered in ecotoxicological studies of Mediterranean cetaceans.
The need for new biomarkers for EDCs and a “cell model” to explore the different
susceptibilities to several classes of ECDs led us to culture fibroblasts of different cetacean
species (“dolphins in test tubes”). Here we propose and apply three new methodological tools
to detect cultured fibroblast responses to OC-EDCs and PBDES: immunofluorescence
technique, western blot and real time PCR. We discuss the preliminary results of the first two.
As “prognostic” tool we explored interspecies and gender susceptibility to OC-EDCs and
qualitative and semi-quantitative evaluation (western blot and
immunofluorescence) of the target proteins CYP1A1 and CYP2B in cultured fibroblasts.
Particular attention was paid to the role of detoxification enzymes (CYP2B) and the related
biochemical susceptibility of the different species to different classes of chemicals. The role
of CYP2B in vitro
metabolism of two tetrachlorobiphenyl congeners were previously
studied in beluga and pilot whale (White et al., 2000).
The main results of these pilot experiments using this non-lethal new investigation tool were
1) The detection of CYP 1A1-1A2 (Fossi personal comunication) and CYP 2B4 in bottlenose
dolphin, striped dolphin and fin whale fibroblasts, revealed by fibroblast immunofluorescence
(Figure 1 A, B, C) and by western blot analysis (Figure 2).
2) Different increases in fluorescence (2B cytochromes) was found between odontocetes and
mysticetes in relation to contaminant doses, with higher induction responses in
dolphin and particularly bottlenose dolphin (Figure 1 A, B) than in fin whale
(Figure 1 C);
3) A gender-related different patterns of induction (cytochromes 2B) of
(Figure 2A) were also found, with higher response capability in male than in female.
4) Increasing doses of contaminants produced increasing induction of CYP2B4, as revealed
by both methodologies (Figure 1,2). Greater induction by PBDE than by OC treatment in
bottlenose dolphin were detected (Figure 2 B). In particular the highest treatment dose of
PBDE, 250 time lower than OCs, was able to produce an induction phenomenon about two
times higher than OCs. These data represent a first worning of the in vitro
potential of this emerging chemicals (PBDE) in cetaceans.
Immunofluorescence: cultured fibroblast from bottlenose dolphin (A
), striped dolphin
), and fin
treated for 48h with a mixture (1, 5, 25 µg/ml) of Arochlor 1260, pp’DDT and pp’DDE in DMSO.
CYP2B4 primary goat anti-rabbit 2B4 P450 antibody was from Oxford Biomedical Research. Arithmetic mean
of Relative Volume Intensity (INT*mm2) are reported for each slides.
. Western blot analysis of CYP2B4 in fibroblast cell culture of (A)
striped dolphins (male and female)
treated for 48h with a mixture (1, 5, 25 µg/ml) of Arochlor 1260, pp’DDT and pp’DDE in DMSO. Western blot
analysis of CYP2B4 in fibroblast cell culture of (B
) bottlenose dolphin treated for 48h with two mixture: a
mixture (1, 5, 25 µg/ml) of Arochlor 1260, pp’DDT and pp’DDE in DMSO; a mixture of 27 PBDEs (0.01,
0.05,0.1 µg/ml), from mono- to deca-brominated, in nonane. CYP2B4 primary goat anti-rabbit 2B4 P450
antibody was from Oxford Biomedical Research. Arithmetic mean of Relative Volume Intensity (INT*mm2) are
In conclusion the information obtained in this pilot experiment will be the basis for further
applications and validation of these methodologies (immunofluorescence, western blot in
cultured cetaceans fibroblasts), integrated with gene expression studies (by real time PCR), to
expolore different species and gender susceptibility of marine mammals to different mixtures
of endocrine disrupting xenobiotics including emerging contaminants.
We thank all the researchers of the Tethys Research Institute, Dr. Serena Porcelloni, Dr. B.
Jimenez and Dr. Ada Natoli for technical support in the sampling and laboratory activities.
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