Expression of μ-, κ- and δ-opioid receptors in P19 mouse embryonal carcinoma cells

被引:31
作者
Chen, HC [1 ]
Wei, LN [1 ]
Loh, HH [1 ]
机构
[1] Univ Minnesota, Dept Pharmacol, Minneapolis, MN 55455 USA
关键词
opioid receptors; P19; embryonal carcinoma cells; retinoic acid; neuronal differentiation; GABA;
D O I
10.1016/S0306-4522(99)00030-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
P19 embryonal carcinoma cells are pluripotential and able to differentiate into a variety of cell types, including neurons, glia and fibroblast-like cells, upon retinoic acid treatment and cellular aggregation. Using reverse transcription-polymerase chain reaction, Ligand binding and immunocytochemical methods, kappa- and delta-opioid receptors were detected in undifferentiated P19 cells. The FL-opioid receptor was not observed until one day after plating, following one essential step of differentiation, but increased in number in the four days after plating. Several different expression patterns were detected in these differentiated cells. Some cells exhibited mu- and delta-opioid receptors co-expressed, with or without K-opioid receptor; whereas some of the cells expressed only K-opioid receptor. All three opioid receptors are detected on aggregated cells which are postmitotic and also expressing neurofilaments, indicating neuronal characteristics. Furthermore, those cells expressing mu- and delta-opioid receptors also expressed glutamate decarboxylase, characteristic of the GABAergic phenotype. Based on these findings, we propose that P19 cells may serve as a model system to study the developmental regulation of opioid receptors, and in particular their relationship with GABA. (C) 1999 IBRO. Published by Elsevier Science Ltd.
引用
收藏
页码:1143 / 1155
页数:13
相关论文
共 41 条
[1]  
AMMER H, 1994, J NEUROCHEM, V62, P1310
[2]   EXPRESSION OF THE GENES-CODING FOR GLUTAMIC-ACID DECARBOXYLASE IN PLURIPOTENT CELL-LINES [J].
BAIN, G ;
RAMKUMAR, TP ;
CHENG, JM ;
GOTTLIEB, DI .
MOLECULAR BRAIN RESEARCH, 1993, 17 (1-2) :23-30
[3]   FROM EMBRYONAL CARCINOMA-CELLS TO NEURONS - THE P19 PATHWAY [J].
BAIN, G ;
RAY, WJ ;
YAO, M ;
GOTTLIEB, DI .
BIOESSAYS, 1994, 16 (05) :343-348
[4]   CHARACTERIZATION OF A TRIPLE OPIOID SYSTEM IN THE HUMAN NEUROBLASTOMA NMB CELL-LINE [J].
BAUMHAKER, Y ;
BENDOR, T ;
BARHAMBURGER, R ;
SARNE, Y .
BRAIN RESEARCH, 1994, 665 (01) :94-100
[5]  
BELKOWSKI SM, 1995, ADV EXP MED BIOL, V373, P11
[6]   A METHOD FOR ISOLATION OF INTACT, TRANSLATIONALLY ACTIVE RIBONUCLEIC-ACID [J].
CATHALA, G ;
SAVOURET, JF ;
MENDEZ, B ;
WEST, BL ;
KARIN, M ;
MARTIAL, JA ;
BAXTER, JD .
DNA-A JOURNAL OF MOLECULAR & CELLULAR BIOLOGY, 1983, 2 (04) :329-335
[7]   NUMBER AND EVOLUTIONARY CONSERVATION OF ALPHA-TUBULIN AND BETA-TUBULIN AND CYTOPLASMIC BETA-ACTIN AND GAMMA-ACTIN GENES USING SPECIFIC CLONED CDNA PROBES [J].
CLEVELAND, DW ;
LOPATA, MA ;
MACDONALD, RJ ;
COWAN, NJ ;
RUTTER, WJ ;
KIRSCHNER, MW .
CELL, 1980, 20 (01) :95-105
[8]   MU-,DELTA-,KAPPA-OPIOID RECEPTORS AND THEIR SUBTYPES - A CRITICAL-REVIEW WITH EMPHASIS ON RADIOLIGAND BINDING EXPERIMENTS [J].
FOWLER, CJ ;
FRASER, GL .
NEUROCHEMISTRY INTERNATIONAL, 1994, 24 (05) :401-426
[9]  
FOWLER CJ, 1994, J COMP NEUROL, V350, P412
[10]   GABAergic synapses on mu-opioid receptor-expressing neurons in the superficial dorsal horn: An electron microscope study in the cat spinal cord [J].
Gong, LW ;
Ding, YQ ;
Wang, D ;
Zheng, HX ;
Qin, BZ ;
Li, JS ;
Kaneko, T ;
Mizuno, N .
NEUROSCIENCE LETTERS, 1997, 227 (01) :33-36