TY - JOUR
T1 - Single and combined effects of heavy metals and hormones on lysosomes of haemolymph cells from the mussel Mytilus galloprovincialis
AU - Viarengo, A.
AU - Marro, A.
AU - Marchi, B.
AU - Burlando, B.
N1 - Funding Information:
Acknowledgements This work was financially supported by the Italian Ministry for University and Scientific Research (MURST). The experiments of this study comply with the current laws of Italy.
PY - 2000
Y1 - 2000
N2 - Effects of heavy metals on lysosomes were studied in living cells from the mussel (Mytilus galloprovincialis Lam.). Haemolymph cells were obtained from the mussel adductor muscle, stained with neutral red (NR), and analysed by digital imaging to evaluate NR retention times within lysosomes. Exposure to Hg2+, Cd2+ and Cu2+ induced a reduction of NR retention time, indicating lysosomal membrane destabilisation. The intensity of these effects was correlated with the metal affinity for sulfhydryls. In contrast, Zn2+ showed no effect on lysosomes. Moreover, 200 μM Zn2+ protected lysosomes against the effects of Cd2+ and Cu2+, but not against Hg2+. Cell loading with the fluorescent pH probe Lyso Sensor followed by digital imaging showed a rise of lysosomal pH induced by Cd2+ and Hg2+, while Zn2+ prevented the effect of Cd2+ and also partially that of Hg2+. The different protective effect of Zn2+ against Hg2+ suggests a dual action of Hg2+ on lysosomes, possibly involving both membrane destabilisation and proton pump inhibition. Cell exposure to 17 β-estradiol also caused a reduction of NR retention time, which was synergistic to that of Hg2+. This suggests a common pathway between metals and hormone, possibly involving Ca2+ signaling.
AB - Effects of heavy metals on lysosomes were studied in living cells from the mussel (Mytilus galloprovincialis Lam.). Haemolymph cells were obtained from the mussel adductor muscle, stained with neutral red (NR), and analysed by digital imaging to evaluate NR retention times within lysosomes. Exposure to Hg2+, Cd2+ and Cu2+ induced a reduction of NR retention time, indicating lysosomal membrane destabilisation. The intensity of these effects was correlated with the metal affinity for sulfhydryls. In contrast, Zn2+ showed no effect on lysosomes. Moreover, 200 μM Zn2+ protected lysosomes against the effects of Cd2+ and Cu2+, but not against Hg2+. Cell loading with the fluorescent pH probe Lyso Sensor followed by digital imaging showed a rise of lysosomal pH induced by Cd2+ and Hg2+, while Zn2+ prevented the effect of Cd2+ and also partially that of Hg2+. The different protective effect of Zn2+ against Hg2+ suggests a dual action of Hg2+ on lysosomes, possibly involving both membrane destabilisation and proton pump inhibition. Cell exposure to 17 β-estradiol also caused a reduction of NR retention time, which was synergistic to that of Hg2+. This suggests a common pathway between metals and hormone, possibly involving Ca2+ signaling.
UR - http://www.scopus.com/inward/record.url?scp=0034510416&partnerID=8YFLogxK
U2 - 10.1007/s002270000391
DO - 10.1007/s002270000391
M3 - Article
SN - 0025-3162
VL - 137
SP - 907
EP - 912
JO - Marine Biology
JF - Marine Biology
IS - 5-6
ER -