REGULATION OF SODIUM CURRENTS AND ACETYLCHOLINE RESPONSES IN PC12 CELLS

被引:39
作者
IFUNE, CK [1 ]
STEINBACH, JH [1 ]
机构
[1] WASHINGTON UNIV,SCH MED,DEPT ANESTHESIOL,BOX 8054,660 S EUCLID AVE,ST LOUIS,MO 63110
关键词
Nerve growth factor; Neuronal differentiation; Pheochromocytoma PC12 cell; Sodium current;
D O I
10.1016/0006-8993(90)91257-H
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Voltage-gated sodium currents and acetylcholine-elicited currents in clonal rat pheochromocytoma cells (PC12) were studied using the whole-cell patch-clamp technique. After treatment of cultures with nerve growth factor (NGF, 2-4 nM) for 5 or more days, both Na currents and ACh responses increased by 5-7 fold. We tested the ability of a number of treatments reported to induce physiological differentiation in neuroblastoma or neuroblastoma-glioma hybrid cells. We found that no treatment was as effective as NGF, and mitotic inhibitors and 8-bromocyclic AMP reduced the efficacy of NGF at increasing both sodium currents and ACh responses. Some treatments were able to selectively reduce or enhance the ability of NGF to induced ACh responses or sodium currents. Dexamethasone, in particular, completely blocked the NGF-induced increase in ACh response, while leaving Na currents unaffected. Furthermore, in individual cells the Na current density and ACh current density are uncorrelated. These observations indicate that physiological differentiation in PC12 cells is regulated differently than in neuroblastoma cells and, further, in PC12 cells sodium currents and ACh responses are independently regulated. © 1990.
引用
收藏
页码:243 / 248
页数:6
相关论文
共 25 条
[1]  
AMY CM, 1983, J NEUROSCI, V3, P1547
[2]  
[Anonymous], 1956, NONPARAMETRIC STAT B
[3]   DEVELOPMENT OF SODIUM-CHANNEL PROTEIN DURING CHEMICALLY-INDUCED DIFFERENTIATION OF NEUROBLASTOMA-CELLS [J].
BAUMGOLD, J ;
SPECTOR, I .
JOURNAL OF NEUROCHEMISTRY, 1987, 48 (04) :1264-1269
[4]   3 TYPES OF ACETYLCHOLINE-INDUCED SINGLE CHANNEL CURRENTS IN CLONAL RAT PHEOCHROMOCYTOMA CELLS [J].
BORMANN, J ;
MATTHAEI, H .
NEUROSCIENCE LETTERS, 1983, 40 (02) :193-197
[5]   ISOLATION OF A CDNA CLONE CODING FOR A POSSIBLE NEURAL NICOTINIC ACETYLCHOLINE-RECEPTOR ALPHA-SUBUNIT [J].
BOULTER, J ;
EVANS, K ;
GOLDMAN, D ;
MARTIN, G ;
TRECO, D ;
HEINEMANN, S ;
PATRICK, J .
NATURE, 1986, 319 (6052) :368-374
[6]   2 DISTINCT KINETIC PHASES OF DESENSITIZATION OF ACETYLCHOLINE-RECEPTORS OF CLONAL RAT PC12-CELLS [J].
BOYD, ND .
JOURNAL OF PHYSIOLOGY-LONDON, 1987, 389 :45-67
[7]   ENHANCEMENT IN EXCITABILITY PROPERTIES OF MOUSE NEUROBLASTOMA-CELLS CULTURED IN PRESENCE OF DIBUTYRYL CYCLIC-AMP [J].
CHALAZONITIS, A ;
GREENE, LA .
BRAIN RESEARCH, 1974, 72 (02) :340-345
[8]   PRIMARY STRUCTURE AND EXPRESSION OF BETA-2 - A NOVEL SUBUNIT OF NEURONAL NICOTINIC ACETYLCHOLINE-RECEPTORS [J].
DENERIS, ES ;
CONNOLLY, J ;
BOULTER, J ;
WADA, E ;
WADA, K ;
SWANSON, LW ;
PATRICK, J ;
HEINEMANN, S .
NEURON, 1988, 1 (01) :45-54
[9]   NERVE GROWTH FACTOR-INDUCED INCREASE IN ELECTRICAL EXCITABILITY AND ACETYLCHOLINE SENSITIVITY OF A RAT PHEOCHROMOCYTOMA CELL LINE [J].
DICHTER, MA ;
TISCHLER, AS ;
GREENE, LA .
NATURE, 1977, 268 (5620) :501-504
[10]  
Greene L. A., 1982, ADV CELL NEUROBIOL, P373, DOI DOI 10.1016/B978-0-12-008303-9.50016-5