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Identification and characterization of parathyroid hormone receptors in rat renal cortical plasma membranes using radioligand binding
Author(s) -
Nickols G. Allen,
MetzNickols Maureen A.,
Roberts M. Scot,
Cooper Cary W.,
Pang Peter K.T.
Publication year - 1989
Publication title -
journal of bone and mineral research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.882
H-Index - 241
eISSN - 1523-4681
pISSN - 0884-0431
DOI - 10.1002/jbmr.5650040420
Subject(s) - parathyroid hormone , radioligand assay , kidney , radioligand , receptor , endocrinology , medicine , chemistry , membrane , parathyroid hormone receptor , biochemistry , biology , hormone receptor , calcium , cancer , breast cancer
Parathyroid hormone (PTH) receptors have been described in renal tissue from several species, but not in the rat. In this study, radioligand binding techniques were used to identify and characterize PTH receptors in rat kidney cortical membranes. The sulfur‐free PTH analog [Nle 8,18 Tyr 34 ]bovine PTH‐(1–34)amide was iodinated using the iodogen method. This ligand was suitable for use in identifying PTH receptors in canine renal membranes, but not rat renal membranes. Synthetic, unsubstituted rat PTH‐(1–34) was iodinated using the milder, lactoperoxidase technique and was purified by HPLC on a C 8 column. [ 125 I]rat PTH‐(1–34) bound rapidly to both rat and dog renal membranes. At 22°C the reaction reached steady state within 20 minutes, and this level was maintained for at least 3 h. Specific binding was routinely >90% for rat kidney and >95% for dog kidney. Similar results were obtained at 4°C with a longer time required to attain steady state (approximately 45 minutes). Binding was reversible as demonstrated by dissociation of bound ligand after either infinite dilution or displacement with excess nonradioactive PTH. Binding was saturable and of high affinity (rat kidney: B max = 2.3 pmol/mg protein, K d = 3.1 nM, dog kidney: B max = 2.1 pmol/mg protein, K d = 3.7 nM). Rat renal cortical adenylate cyclase activity was stimulated by rat PTH in a dose‐dependent manner with an EC 50 of 4 nM, a value in good agreement with the binding data. This study demonstrates the feasibility of identifying and characterizing parathyroid hormone receptors in rat renal cortical plasma membranes using radioligand binding techniques.