Item Type: | Article |
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Title: | Megalin antagonizes activation of the parathyroid hormone receptor |
Creators Name: | Hilpert, J., Nykjaer, A., Jacobsen, C., Wallukat, G., Nielsen, R., Moestrup, S.K., Haller, H., Luft, F.C., Christensen, E.I. and Willnow, T.E. |
Abstract: | Parathyroid hormone (PTH) is predominantly cleared from the circulation by glomerular filtration and degradation in the renal proximal tubules. Here, we demonstrate that megalin, a multifunctional endocytic receptor in the proximal tubular epithelium, mediates the uptake and degradation of PTH. Megalin was purified from kidney membranes as the major PTH-binding protein and shown in BIAcore analysis to specifically bind full-length PTH and amino-terminal PTH fragments (Kd 0.5 microM). Absence of the receptor in megalin knockout mice resulted in 4-fold increased levels of amino-terminal PTH fragments in the urine. In F9 cells expressing both megalin and the PTH/PTH-related peptide receptor (PTH/PTHrP receptor), uptake and lysosomal degradation of the hormone was mediated through megalin. Blocking megalin-mediated clearance of PTH resulted in 3-fold increased stimulation of the PTH/PTHrP receptor. These data provide evidence that megalin is involved in the renal catabolism of PTH and potentially antagonizes PTH/PTHrP receptor activity in the proximal tubular epithelium. |
Keywords: | Base Sequence, Cattle, Cultured Tumor Cells, DNA Primers, Heymann Nephritis Antigenic Complex, Immunohistochemistry, Kidney, Membrane Glycoproteins, Molecular Cloning, Parathyroid Hormone, Parathyroid Hormone Receptors, Animals, Mice, Rats |
Source: | Journal of Biological Chemistry |
ISSN: | 0021-9258 |
Publisher: | American Society for Biochemistry and Molecular Biology |
Volume: | 274 |
Number: | 9 |
Page Range: | 5620-5625 |
Date: | 26 February 1999 |
Official Publication: | https://doi.org/10.1074/jbc.274.9.5620 |
PubMed: | View item in PubMed |
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