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
相关论文
共 34 条
[11]   PARATHYROID HORMONE-RELATED PROTEIN - ELEVATED LEVELS IN BOTH HUMORAL HYPERCALCEMIA OF MALIGNANCY AND HYPERCALCEMIA COMPLICATING METASTATIC BREAST-CANCER [J].
GRILL, V ;
HO, P ;
BODY, JJ ;
JOHANSON, N ;
LEE, SC ;
KUKREJA, SC ;
MOSELEY, JM ;
MARTIN, TJ .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1991, 73 (06) :1309-1315
[12]   RE-EXAMINATION AND FURTHER DEVELOPMENT OF A PRECISE AND RAPID DYE METHOD FOR MEASURING CELL-GROWTH CELL KILL [J].
HANSEN, MB ;
NIELSEN, SE ;
BERG, K .
JOURNAL OF IMMUNOLOGICAL METHODS, 1989, 119 (02) :203-210
[13]   REGULATION OF PROLIFERATION IN JEG-3 CELLS BY A 500-KDA CA2+ SENSOR AND PARATHYROID HORMONE-RELATED PROTEIN [J].
HELLMAN, P ;
HELLMAN, B ;
JUHLIN, C ;
JUPPNER, H ;
RASTAD, J ;
RIDEFELT, P ;
AKERSTROM, G .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1993, 307 (02) :379-385
[14]  
HENDERSON J, 1991, CANCER RES, V51, P6521
[15]   Reduced immunostaining for the extracellular Ca sensing receptor in primary and uremic secondary hyperparathyroidism [J].
Kifor, O ;
Moore, FD ;
Wang, P ;
Goldstein, M ;
Vassilev, P ;
Kifor, I ;
Hebert, SC ;
Brown, EM .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1996, 81 (04) :1598-1606
[16]   The calcium-sensing receptor is localized in caveolin-rich plasma membrane domains of bovine parathyroid cells [J].
Kifor, O ;
Diaz, R ;
Butters, R ;
Kifor, I ;
Brown, EM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (34) :21708-21713
[17]   Parathyroid-hormone-related peptide in hematologic malignancies [J].
Kremer, R ;
Shustik, C ;
Tabak, T ;
Papavasiliou, V ;
Goltzman, D .
AMERICAN JOURNAL OF MEDICINE, 1996, 100 (04) :406-411
[18]   Elevated extracellular calcium can prevent apoptosis via the calcium-sensing receptor [J].
Lin, KI ;
Chattopadhyay, N ;
Bai, M ;
Alvarez, R ;
Dang, CV ;
Baraban, JM ;
Brown, EM ;
Ratan, RR .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 249 (02) :325-331
[19]   Mechanism of extracellular Ca2+ receptor-stimulated hormone release from sheep thyroid parafollicular cells [J].
McGehee, DS ;
Aldersberg, M ;
Liu, KP ;
Hsuing, SC ;
Heath, MJS ;
Tamir, H .
JOURNAL OF PHYSIOLOGY-LONDON, 1997, 502 (01) :31-44
[20]   Functional calcium-sensing receptor expression in ovarian surface epithelial cells [J].
McNeil, L ;
Hobson, S ;
Nipper, V ;
Rodland, KD .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1998, 178 (02) :305-313