Extracellular calcium-sensing receptor (CaR) expression and its potential role in parathyroid hormone-related peptide (PTHrP) secretion in the H-500 rat leydig cell model of humoral hypercalcemia of malignancy

被引:36
作者
Sanders, JL
Chattopadhyay, N
Kifor, O
Yamaguchi, T
Brown, EM
机构
[1] Brigham & Womens Hosp, Div Endocrine Hypertens, Dept Med, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA 02115 USA
关键词
CaR; PTHrP secretion; humoral hypercalcemia of malignancy; leydig cell cancer; H-500 leydig cells;
D O I
10.1006/bbrc.2000.2157
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Humoral hypercalcemia of malignancy (HHM) occurs when secretion of parathyroid hormone-related peptide (PTHrP) by cancer cells causes hypercalcemia in the absence of skeletal metastases. High extracellular calcium (Ca-o(2+)) increases secretion of PTH-like bioactivity by rat H-500 leydig cells, a transplantable model of HHM, an action potentially mediated by the Ca-o(2+)-sensing receptor (CaR). In this study we investigated whether H-500 cells express the CaR and, if so, whether CaR agonists modulate PTHrP secretion. Northern blot analysis and RT-PCR revealed bona fide CaR transcript(s), and immunocytochemistry and Western analysis with a specific anti-CaR antiserum demonstrated CaR protein expression in H-500 cells. Furthermore, high Ca-o(2+) and neomycin stimulated PTHrP secretion dose-dependently with maximal 2.7- and 3.3-fold increases at 5 mM Ca-o(2+) and 300 mu M neomycin, respectively. Thus in HHM caused by H-500 cells, the CaR could participate in a vicious cycle whereby PTHrP-induced increases in Ca-o(2+) further stimulate PTHrP release and exacerbate hypercalcemia. (C) 2000 Academic Press.
引用
收藏
页码:427 / 432
页数:6
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