1,25-(OH)2 VITAMIN-D-3 ENHANCES PAF-STIMULATED CALCIUM MOBILIZATION IN U937 CELLS BY EXPRESSION OF SPECIFIC PAF BINDING-SITES

被引:13
作者
AEPFELBACHER, M
KORTH, R
WEBER, PC
机构
[1] Institut für Prophylaxe und Epidemiologie der Kreislaufkrankheiten, Universität München, München
关键词
(Human cell); (U937 cell); 1,25-Dihydroxycholecalciferol; Calcium ion mobilization; Cell maturation; Leukotriene D[!sub]4[!/sub; PAF receptors; Vitamin D-3;
D O I
10.1016/0167-4889(90)90191-F
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
The effect of 1,25-(OH)2 vitamin D-3 (10 nM, 72 h) on cytosolic free Ca2+ concentration ([Ca2+]i) in U937 cells before and after stimulation with Paf, LTD4 and ADP was investigated. 1,25-(OH)2 vitamin D-3 increased basal [Ca2+]i from 98 ± 1 nM to 121 ± 5 nM (P < 0.01) and the Paf (10 nM) stimulated increase in [Ca2+]i from 143 ± 15 to 406 ± 44 nM (P < 0.01). These vitamin D-3 effects were time-related and occurred after 24 h (basal [Ca2+]i) and 12 h (Paf stimulated Ca2+-mobilization) but not after 3 h. In comparison, vitamin D-3 failed to modulate Ca2+-mobilization in response to ADP (1-40 μM) and increased it only in response to low leukotriene D4 concentrations (0.1-1 nM). The total binding of [3H]Paf (2.8 nM) was not significantly different in untreated vs. vitamin D-3-treated cells. However, the Paf receptor antagonist Web 2086 (1 μM) inhibited [3H]Paf binding only in vitamin D-3-treated cells. The specific binding reached a plateau of 28 ± 3 fmol per 2.5 · 106 cells between 1.4 and 2.8 nM [3H]Paf. The Paf receptor antagonist Web 2086 (1-1000 nM) also inhibited the Paf-mediated Ca2+-mobilization in vitamin D-3-treated cells (IC50 = 191 ± 55 M). These data suggest that the enhanced Ca2+-mobilization in vitamin D-3-treated U937 cells in response to Paf is mediated by an expression of putative Paf receptors. © 1990.
引用
收藏
页码:179 / 184
页数:6
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