Selective c-Jun overexpression is associated with ionizing radiation-induced apoptosis in the developing cerebellum of the rat

被引:46
作者
Ferrer, I
Olive, M
Blanco, R
Cinos, C
Planas, AM
机构
[1] HOSP DURAN & REYNALS, LHOSPITALET DE LLOBREGAT, SPAIN
[2] CSIC, CID, DEPT FARMACOL & TOXICOL, BARCELONA, SPAIN
来源
MOLECULAR BRAIN RESEARCH | 1996年 / 38卷 / 01期
关键词
Bcl-2; Bax; c-Myc; Fos; Jun; apoptosis; cell death; ionizing radiation; development; nervous system;
D O I
10.1016/0169-328X(95)00334-O
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Immunohistochemistry to Bcl-2, Bax, c-Myc, c-Fos, Fos-related, c-Jun, Jun B and Jun D was used to study the involvement of these factors in ionizing radiation-induced apoptosis in the cerebellum of the developing rat. Selective c-Jun overexpression was observed during the whole process of radiation-induced cell death. Furthermore, c-Jun overexpression was restricted to apoptotic cells, as shown by double labeling with the method of in situ labeling of nuclear DNA fragmentation and c-Jun immunohistochemistry. This is the first in vivo evidence that selective c-Jun overexpression is associated with apoptotic cell death in the developing nervous system following ionizing radiation.
引用
收藏
页码:91 / 100
页数:10
相关论文
共 69 条
  • [1] BCL-2 GENE IS HIGHLY EXPRESSED DURING NEUROGENESIS IN THE CENTRAL-NERVOUS-SYSTEM
    ABEDOHMAE, S
    HARADA, N
    YAMADA, K
    TANAKA, R
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 191 (03) : 915 - 921
  • [2] THE PROTOONCOGENE BCL-2 CAN SELECTIVELY RESCUE NEUROTROPHIC FACTOR-DEPENDENT NEURONS FROM APOPTOSIS
    ALLSOPP, TE
    WYATT, S
    PATERSON, HF
    DAVIES, AM
    [J]. CELL, 1993, 73 (02) : 295 - 307
  • [3] THE C-MYC PROTEIN INDUCES CELL-CYCLE PROGRESSION AND APOPTOSIS THROUGH DIMERIZATION WITH MAX
    AMATI, B
    LITTLEWOOD, TD
    EVAN, GI
    LAND, H
    [J]. EMBO JOURNAL, 1993, 12 (13) : 5083 - 5087
  • [4] EXPRESSION OF C-FOS AND C-JUN FAMILY GENES AFTER FOCAL CEREBRAL-ISCHEMIA
    AN, G
    LIN, TN
    LIU, JS
    XUE, JJ
    HE, YY
    HSU, CY
    [J]. ANNALS OF NEUROLOGY, 1993, 33 (05) : 457 - 464
  • [5] THE JUN PROTO-ONCOGENE IS POSITIVELY AUTOREGULATED BY ITS PRODUCT, JUN/AP-1
    ANGEL, P
    HATTORI, K
    SMEAL, T
    KARIN, M
    [J]. CELL, 1988, 55 (05) : 875 - 885
  • [6] THE ROLE OF JUN, FOS AND THE AP-1 COMPLEX IN CELL-PROLIFERATION AND TRANSFORMATION
    ANGEL, P
    KARIN, M
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1072 (2-3) : 129 - 157
  • [7] ONCOGENE JUN ENCODES A SEQUENCE-SPECIFIC TRANS-ACTIVATOR SIMILAR TO AP-1
    ANGEL, P
    ALLEGRETTO, EA
    OKINO, ST
    HATTORI, K
    BOYLE, WJ
    HUNTER, T
    KARIN, M
    [J]. NATURE, 1988, 332 (6160) : 166 - 171
  • [8] HUMAN PROTOONCOGENE C-JUN ENCODES A DNA-BINDING PROTEIN WITH STRUCTURAL AND FUNCTIONAL-PROPERTIES OF TRANSCRIPTION FACTOR AP-1
    BOHMANN, D
    BOS, TJ
    ADMON, A
    NISHIMURA, T
    VOGT, PK
    TJIAN, R
    [J]. SCIENCE, 1987, 238 (4832) : 1386 - 1392
  • [9] BCL-2 MESSENGER-RNA IS LOCALIZED IN NEURONS OF THE DEVELOPING AND ADULT-RAT BRAIN
    CASTREN, E
    OHGA, Y
    BERZAGHI, MP
    TZIMAGIORGIS, G
    THOENEN, H
    LINDHOLM, D
    [J]. NEUROSCIENCE, 1994, 61 (01) : 165 - 177
  • [10] JUN-B DIFFERS IN ITS BIOLOGICAL PROPERTIES FROM, AND IS A NEGATIVE REGULATOR OF, C-JUN
    CHIU, R
    ANGEL, P
    KARIN, M
    [J]. CELL, 1989, 59 (06) : 979 - 986