Immunochemical and immunohistochemical localization of Bcl-x protein in the rat central nervous system

被引:32
作者
Mizuguchi, M
Sohma, O
Takashima, S
Ikeda, K
Yamada, M
Shiraiwa, N
Ohta, S
机构
[1] TOKYO INST PSYCHIAT,DEPT ULTRASTRUCT & HISTOCHEM,TOKYO,JAPAN
[2] NIIGATA UNIV,BRAIN RES INST,DEPT PATHOL,NIIGATA,JAPAN
[3] JICHI MED SCH,DEPT BIOCHEM,MINAMI KAWACHI,TOCHIGI,JAPAN
[4] NIPPON MED COLL,INST GERONTOL,DIV BIOCHEM,KAWASAKI,KANAGAWA,JAPAN
关键词
apoptosis; neuron; glial cell; development; immunohistochemistry; western blotting;
D O I
10.1016/0006-8993(95)01453-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
To explore the role of bcl-x in the regulation of cell death in the nervous system, we produced monoclonal antibodies against rat Bcl-x(L) protein, the major product of the rat bcl-x gene that inhibits apoptosis, and defined its distribution in rat neural tissues by immunochemical and immunohistochemical means. Western blotting of tissue homogenates identified the Bcl-x protein as two bands with molecular weights of about 29 and 31 kDa. The level of Bcl-x expression in the nervous system was high, being comparable to that in the hematolymphoid system, and higher in the fetal than in the adult brain. Subcellular fractionation studies localized Bcl-x to various subcellular compartments. In tissue culture, Bcl-x was produced by all the cell types examined, including neurons, astrocytes, oligodendrocytes and microglial cells. Immunohistochemistry revealed that Bcl-x immunoreactivity was more intense in the gray than in the white matter. In the fetal cerebral cortex, labeling was mostly confined to the neuronal perikarya, whereas in the more mature brain, the neuropil of the gray matter, as well as the glial cells in the white matter, was also stained.
引用
收藏
页码:281 / 286
页数:6
相关论文
共 31 条
[1]   BCL-2 GENE IS HIGHLY EXPRESSED DURING NEUROGENESIS IN THE CENTRAL-NERVOUS-SYSTEM [J].
ABEDOHMAE, S ;
HARADA, N ;
YAMADA, K ;
TANAKA, R .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 191 (03) :915-921
[2]   BCL-X, A BCL-2-RELATED GENE THAT FUNCTIONS AS A DOMINANT REGULATOR OF APOPTOTIC CELL-DEATH [J].
BOISE, LH ;
GONZALEZGARCIA, M ;
POSTEMA, CE ;
DING, LY ;
LINDSTEN, T ;
TURKA, LA ;
MAO, XH ;
NUNEZ, G ;
THOMPSON, CB .
CELL, 1993, 74 (04) :597-608
[3]   INDUCTION OF APOPTOSIS BY THE BCL-2 HOMOLOG BAK [J].
CHITTENDEN, T ;
HARRINGTON, EA ;
OCONNOR, R ;
FLEMINGTON, C ;
LUTZ, RJ ;
EVAN, GI ;
GUILD, BC .
NATURE, 1995, 374 (6524) :733-736
[4]  
FANG W, 1994, J IMMUNOL, V153, P4388
[5]   CLONING OF A BCL-2 HOMOLOG BY INTERACTION WITH ADENOVIRUS E1B 19K [J].
FARROW, SN ;
WHITE, JHM ;
MARTINOU, I ;
RAVEN, T ;
PUN, KT ;
GRINHAM, CJ ;
MARTINOU, JC ;
BROWN, R .
NATURE, 1995, 374 (6524) :731-733
[6]   INCREASED EXPRESSION OF BCL-2 IMMUNOREACTIVITY IN THE DEVELOPING CEREBRAL-CORTEX OF THE RAT [J].
FERRER, I ;
TORTOSA, A ;
CONDOM, E ;
BLANCO, R ;
MACAYA, A ;
PLANAS, A .
NEUROSCIENCE LETTERS, 1994, 179 (1-2) :13-16
[7]  
GONZALEZGARCIA M, 1994, DEVELOPMENT, V120, P3033
[8]  
GOTTSCHALK AR, 1994, P NATL ACAD SCI USA, V91, P7530
[9]   INACTIVATION OF BCL-2 BY PHOSPHORYLATION [J].
HALDAR, S ;
JENA, N ;
CROCE, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (10) :4507-4511
[10]   BCL2 PROTEIN IS TOPOGRAPHICALLY RESTRICTED IN TISSUES CHARACTERIZED BY APOPTOTIC CELL-DEATH [J].
HOCKENBERY, DM ;
ZUTTER, M ;
HICKEY, W ;
NAHM, M ;
KORSMEYER, SJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (16) :6961-6965