A new factor derived from 1321N1 human astrocytoma cells causes differentiation of PC-12 cells mediated through mitogen-activated protein kinase cascade

被引:22
作者
Obara, Y [1 ]
Nakahata, N [1 ]
Ohizumi, Y [1 ]
机构
[1] Tohoku Univ, Fac Pharmaceut Sci, Dept Pharmaceut Mol Biol, Aoba Ku, Sendai, Miyagi 9808578, Japan
关键词
1321N1 human astrocytoma cells; PC-12; cells; neurotrophic factor; neurite outgrowth; mitogen-activated protein kinase;
D O I
10.1016/S0006-8993(98)00731-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Glial cells play an important role in maintaining neural function. In the present study, we examined the effects of a factor derived from human astrocytoma cells (1321N1) on differentiation of rat pheochromocytoma cells (PC-12). The conditioned medium which had been used for culture of 1321N1 cells caused the differentiation of PC-12 cells, suggesting that 1321N1 cells release a neurotrophic factor. The factor was apparently distinct from well-known neurotrophic factors, such as nerve growth factor (NGF), since it was resistant to boiling and trypsin treatment. The molecular size of the factor was assumed to be below 1000 through dialysis and ultrafiltration experiments. Furthermore, PC-12 cells were differentiated synergistically by the combined addition of NGF and the conditioned medium of 1321N1 cells. Partially purified fraction of the factor by Sephadex G-15 gel filtration column caused the prolonged activation of mitogen-activated protein kinase (MAPK). The differentiation of PC-12 cells induced by the fraction or NGF disappeared after the treatment with PD98059, a specific inhibitor of MAPK kinase (MEK), suggesting the involvement of MAPK in the differentiation. These results suggest that the new low-molecular factor derived from glial cells causes differentiation of PC-12 cells mediated through an activation of MAPK. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:79 / 88
页数:10
相关论文
共 47 条
[11]   NEURONS AND ASTROCYTES INFLUENCE THE DEVELOPMENT OF PURIFIED O-2A PROGENITOR CELLS [J].
DUTLY, F ;
SCHWAB, ME .
GLIA, 1991, 4 (06) :559-571
[12]   LONG-TERM INCREASES IN NEUROTRANSMITTER RELEASE FROM NEURONAL CELLS EXPRESSING A CONSTITUTIVELY ACTIVE ADENYLATE-CYCLASE FROM A HERPES-SIMPLEX VIRUS TYPE-1 VECTOR [J].
GELLER, AI ;
DURING, MJ ;
HAYCOCK, JW ;
FREESE, A ;
NEVE, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (16) :7603-7607
[13]   CATECHOLAMINE-INDUCED ALTERATION IN SEDIMENTATION BEHAVIOR OF MEMBRANE-BOUND BETA-ADRENERGIC RECEPTORS [J].
HARDEN, TK ;
COTTON, CU ;
WALDO, GL ;
LUTTON, JK ;
PERKINS, JP .
SCIENCE, 1980, 210 (4468) :441-443
[14]   EVIDENCE THAT MUSCARINIC CHOLINERGIC RECEPTORS SELECTIVELY INTERACT WITH EITHER THE CYCLIC-AMP OR THE INOSITOL PHOSPHATE 2ND-MESSENGER RESPONSE SYSTEMS [J].
HEPLER, JR ;
HUGHES, AR ;
HARDEN, TK .
BIOCHEMICAL JOURNAL, 1987, 247 (03) :793-796
[15]   NEUROFILAMENT GENE-EXPRESSION - A MAJOR DETERMINANT OF AXONAL CALIBER [J].
HOFFMAN, PN ;
CLEVELAND, DW ;
GRIFFIN, JW ;
LANDES, PW ;
COWAN, NJ ;
PRICE, DL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (10) :3472-3476
[16]   A novel differentiation factor for PC12 cells from culture supernatant of mouse hepatocyte cell line MLE-15A2 [J].
Ihara, S ;
Nishikawa, T ;
Kimura, K ;
Fujiyoshi, T ;
Shirai, T ;
Komi, A ;
Kanda, H ;
Yamori, T ;
Fukui, Y .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 1996, 60 (08) :1339-1345
[17]   A comparative study of arachidonic acid metabolism in rabbit cultured astrocytes and human astrocytoma cells (1321N1) [J].
Ishimoto, H ;
Matsuoka, I ;
Nakanishi, H ;
Nakahata, N .
GENERAL PHARMACOLOGY-THE VASCULAR SYSTEM, 1996, 27 (02) :313-317
[18]  
ITO E, 1989, ONCOGENE, V4, P1193
[19]   EXPRESSION AND STRUCTURE OF THE HUMAN NGF RECEPTOR [J].
JOHNSON, D ;
LANAHAN, A ;
BUCK, CR ;
SEHGAL, A ;
MORGAN, C ;
MERCER, E ;
BOTHWELL, M ;
CHAO, M .
CELL, 1986, 47 (04) :545-554
[20]  
Jonakait G M, 1997, Adv Pharmacol, V37, P35