Megalin-Dependent Internalization of Cadmium-Metallothionein and Cytotoxicity in Cultured Renal Proximal Tubule Cells

• Published in: The Journal of pharmacology and experimental therapeutics 2006-08, Vol.318 (2), p.782-791
• Main Authors: Wolff, Natascha A, Abouhamed, Marouan, Verroust, Pierre J, Thévenod, Frank
• Format: Article
• Language: English
• Subjects: Animals; Blotting, Western; Cell Line; Cell Survival - drug effects; Cells, Cultured; Fluorescent Antibody Technique; Fluorescent Dyes; GTP-Binding Proteins - isolation & purification; GTP-Binding Proteins - metabolism; Humans; Immunoglobulin G - immunology; Immunoglobulin G - isolation & purification; Kidney Tubules, Proximal - cytology; Kidney Tubules, Proximal - drug effects; Kidney Tubules, Proximal - metabolism; Kinetics; Low Density Lipoprotein Receptor-Related Protein-2 - biosynthesis; Low Density Lipoprotein Receptor-Related Protein-2 - metabolism; Low Density Lipoprotein Receptor-Related Protein-2 - physiology; Maleimides; Metallothionein - metabolism; Rabbits; Rats; Receptors, Cell Surface - biosynthesis; Reverse Transcriptase Polymerase Chain Reaction
• ISSN: 0022-3565; 1521-0103
• DOI: 10.1124/jpet.106.102574

Chronic cadmium (Cd 2+ ) exposure results in renal proximal tubular cell damage. Delivery of Cd 2+ to the kidney occurs mainly as complexes with metallothionein-1 (molecular mass ∼ 7 kDa), freely filtered at the glomerulus. For Cd 2+ to gain access to the proximal tubule cells, these complexes are thought to be internalized via receptors for small protein ligands, such as megalin and cubilin, followed by release of Cd 2+ from metallothionein-1 in endosomal/lysosomal compartments. To investigate the role of megalin in renal cadmium-metallothionein-1 reabsorption, megalin expression and dependence of cadmium-metallothionein-1 internalization and cytotoxicity on megalin were studied in a renal proximal tubular cell model (WKPT-0293 Cl.2 cells). Expression of megalin was detected by reverse transcriptase-polymerase chain reaction and visualized by immunofluorescence both at the cell surface (live staining) and intracellularly (permeabilized cells). Internalization of Alexa Fluor 488-coupled metallothionein-1 was concentration-dependent, saturating at approximately 15 μM. At 14.3 μM, metallothionein-1 uptake could be significantly attenuated by 30.9 ± 6.6% ( n = 4) by 1 μM of the receptor-associated protein (RAP) used as a competitive inhibitor of cadmium-metallothionein-1 binding to megalin and cubilin. Consistently, cytotoxicity of a 24-h treatment with 7.14 μM cadmium-metallothionein-1 was significantly reduced by 41.0 ± 7.6%, 61.6 ± 3.4%, and 26.2 ± 1.8% ( n = 4-5 each) by the presence of 1 μM RAP, 400 μg/ml anti-megalin antibody, or 5 μM of the cubilin-specific ligand, apo-transferrin, respectively. Cubilin expression in proximal tubule cells was also confirmed at the mRNA and protein level. The data indicate that renal proximal tubular cadmium-metallothionein-1 uptake and cell death are mediated at least in part by megalin.