F281, synthetic agonist of the sigma-2 receptor, induces Ca2+ efflux from the endoplasmic reticulum and mitochondria in SK-N-SH cells

被引:44
作者
Cassano, Giuseppe [1 ]
Gasparre, Giuseppe [1 ]
Niso, Mauro [2 ]
Contino, Marialessandra [2 ]
Scalera, Vito [1 ]
Colabufo, Nicola Antonio [2 ]
机构
[1] Univ Bari, Dipartimento Fisiol Gen Ambientale, I-70126 Bari, Italy
[2] Univ Bari, Dipartimento Farmacochim, I-70125 Bari, Italy
关键词
Endoplasmic reticulum; Mitochondria; Neuromodulation; Receptor; Tumour; OPERATED CALCIUM-ENTRY; INTRACELLULAR CA2+; RELEASE; LIGANDS; STORE; EXPRESSION; TRANSPORT; CANCER; DRUGS; ACID;
D O I
10.1016/j.ceca.2008.12.005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We demonstrate that F281, a synthetic agonist of the sigma-2 receptor (s2R), induces a non transient increase in intracellular [Ca2+] ([Ca2+](i)) and cell death in SK-N-SH cells. Sigma receptors are classified into two subtypes, with different molecular weight and tissue distribution. While the sigma-1 receptor has been cloned, the s2r is less characterized and its physiological ligand and role need further investigation. In turnout cell lines, synthetic agonists of the s2R trigger apoptosis and modulate [Ca2+](i). In particular, CB-64D induces a Ca2+ response while PB28 supresses Ca2+ signalling. We have recently synthesized F281, by replacing the 5-methoxytetraline moiety of PB28 with a carbazole nucleus. Although this bioisosteric substitution should not affect the ligand affinity at the receptor, F281 (after 24 h incubation) was more cytotoxic than PB28 (EC50 values 65.4 nM and 8.13 mu M, respectively) in SK-N-SH cells. We used the fluorescent probes fura-2, rhod-2 and JC-1. F281 mobilizes Ca2+ from mitochondria and from the endoplasmic reticulum, by opening its inositol 1,4,5-trisphosphate receptor; Ca2+-entry through the channels activated by store depletion was also observed. After the increase in [Ca2+](i) and within 10 min, we observed a sudden drop in metabolic activity and intracellular [ATP] leading to cell death. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:340 / 345
页数:6
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