| Literature DB >> 10026179 |
J Hilpert1, A Nykjaer, C Jacobsen, G Wallukat, R Nielsen, S K Moestrup, H Haller, F C Luft, E I Christensen, T E Willnow.
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.Entities:
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Year: 1999 PMID: 10026179 DOI: 10.1074/jbc.274.9.5620
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157