Role of placental metallothionein in maternal to fetal transfer of cadmium in genetically altered mice

• Published in: Toxicology (Amsterdam) Vol. 127; no. 1; pp. 167 - 178
• Main Authors: Lau, John C, Joseph, Mariamma G, Cherian, M.George
• Format: Journal Article
• Language: English
• Published: Shannon Elsevier Ireland Ltd 15-05-1998; Amsterdam Elsevier Science
• Subjects: Animals; Biological and medical sciences; Biological Transport; Cadmium; Cadmium - metabolism; Cadmium - pharmacokinetics; Cadmium Radioisotopes; Chemical and industrial products toxicology. Toxic occupational diseases; Chromatography, Gel; Copper - analysis; Distribution; Female; Fetus - metabolism; Immunohistochemistry; Kidney - embryology; Kidney - metabolism; Liver - embryology; Liver - metabolism; Maternal-Fetal Exchange; Medical sciences; Metallothionein; Metallothionein - genetics; Metallothionein - metabolism; Metals and various inorganic compounds; Mice; Mice, Inbred C57BL; Placenta - metabolism; Placental transfer; Pregnancy; Toxicology; Transgenic mice; Uterus - metabolism; Zinc - analysis; Immunohistochemistry; Cadmium; Placental transfer; Metallothionein; Distribution; Transgenic mice; Toxicity; Rodentia; Transgenic animal; Heavy metal; Toxicokinetics; Vertebrata; Mammalia; Mother embryonal transfer; Mouse; Pharmacokinetics
• ISSN: 0300-483X; 1879-3185
• DOI: 10.1016/S0300-483X(98)00028-6

The role of placental metallothionein (MT) as a barrier for maternal to fetal transfer of cadmium (Cd) was investigated using mice which overexpressed the MT-1 isoform (MT-1*), mice which did not express the MT-1 and 2 isoforms (MT-null) and control mice (C57BL/6). In addition, immunohistochemical localization of MT in the placenta was determined in these mice. Two days prior to parturition, the mice were injected with radioactive
109Cd chloride (4
μCi, 0.6 ng Cd/mouse) and killed 24 h later. Organs and fetuses were collected and radioactivity, MT and metal levels were measured. Cd accumulated mainly in the liver and kidney (80% of administered dose) with very low levels (0.1–0.3%) detected in fetuses. When analyzed on a per organ or per gram basis, MT-null fetuses accumulated significantly more Cd (3–10-fold) than the control fetuses and there was no significant difference in fetal Cd accumulation in the MT-1* and control fetuses. As expected, MT and zinc levels were higher in MT-1* than C57BL/6 mice and no MT was detected in MT-null mice. Most striking was the high hepatic MT levels in MT-1* dams (4 mg/g). Immunohistochemical analysis showed MT staining in spongiotrophoblasts, glycogen cells, visceral yolk sac, trophoblast giant cells and maternal decidual cells with the MT-1* placenta staining much more intensely as compared to control placenta. The results suggest that placental MT reduces maternal to fetal Cd transfer, however the low doses of Cd administered in the present experiment resulted in high levels of Cd accumulation in liver and kidney in all groups of mice with a low concentration of Cd reaching the placenta. Thus, the role of placental MT as a barrier for Cd is inconclusive.