CELL-CYCLE ARREST OF PROLIFERATING NEURONAL CELLS BY SERUM DEPRIVATION CAN RESULT IN EITHER APOPTOSIS OR DIFFERENTIATION

被引:101
作者
HOWARD, MK
BURKE, LC
MAILHOS, C
PIZZEY, A
GILBERT, CS
LAWSON, WD
COLLINS, MKL
THOMAS, NSB
LATCHMAN, DS
机构
[1] UNIV COLL & MIDDLESEX SCH MED,DEPT BIOCHEM,DIV MOLEC PATHOL,MED MOLEC BIOL UNIT,LONDON W1P 6DP,ENGLAND
[2] INST CANC RES,CHESTER BEATTY LABS,LONDON,ENGLAND
[3] UNIV COLL & MIDDLESEX SCH MED,DEPT HAEMATOL,LONDON,ENGLAND
[4] UNIV LONDON UNIV COLL,IMPERIAL CANC RES FUND LABS,LONDON WC1E 6BT,ENGLAND
[5] UNIV LONDON UNIV COLL,DEPT BIOL,LONDON WC1E 6BT,ENGLAND
关键词
CELL DEATH; NEURONAL CELLS; APOPTOSIS; DIFFERENTIATION; SERUM DEPRIVATION; CELL CYCLE ARREST;
D O I
10.1111/j.1471-4159.1993.tb13404.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Apoptotic cell death plays a critical role in the development of the nervous system. The death of mature nondividing neurons that fail to receive appropriate input from the target field has been extensively studied. However, the mechanisms mediating the extensive cell death occurring in areas of the developing brain where proliferating neuroblasts differentiate into mature nondividing neurons have not been analyzed. We show here that the cell cycle arrest of a proliferating cell of neuronal origin by removal of serum results in either apoptotic cell death or differentiation to a mature nondividing neuronal cell. The proportion of cells undergoing death or differentiation is influenced in opposite directions by treatment of the cells with cyclic AMP and retinoic acid. This suggests that following the withdrawal of signals stimulating neuroblast cell division, neuronal cells either can cease to suppress a constitutive suicide pathway and hence die by apoptosis or, alternatively, can differentiate into a mature neuronal cell. Regulation of the balance between apoptosis and neuronal differentiation could therefore play a critical role in controlling the numbers of mature neurons that form.
引用
收藏
页码:1783 / 1791
页数:9
相关论文
共 31 条
[1]   RETINOIC-ACID-INDUCED LIMB-REDUCTION DEFECTS - PERTURBATION OF ZONES OF PROGRAMMED CELL-DEATH AS A PATHOGENETIC MECHANISM [J].
ALLES, AJ ;
SULIK, KK .
TERATOLOGY, 1989, 40 (02) :163-171
[2]   TROPHIC FACTORS AND NEURONAL SURVIVAL [J].
BARDE, YA .
NEURON, 1989, 2 (06) :1525-1534
[3]  
BURKE LC, 1992, ONCOGENE, V7, P783
[4]   CELL-CYCLE REGULATION [J].
BYBEE, A ;
THOMAS, NSB .
BLOOD REVIEWS, 1991, 5 (03) :177-192
[5]  
CARR VM, 1982, DEV BRAIN RES, V2, P157
[6]   PROLIFERATION AND DIFFERENTIATION OF NEURONAL STEM-CELLS REGULATED BY NERVE GROWTH-FACTOR [J].
CATTANEO, E ;
MCKAY, R .
NATURE, 1990, 347 (6295) :762-765
[7]   CELL HETEROGENEITY DURING THE CELL-CYCLE [J].
DARZYNKIEWICZ, Z ;
CRISSMAN, H ;
TRAGANOS, F ;
STEINKAMP, J .
JOURNAL OF CELLULAR PHYSIOLOGY, 1982, 113 (03) :465-474
[8]   GENETIC-CONTROL OF PROGRAMMED CELL-DEATH IN THE NEMATODE C-ELEGANS [J].
ELLIS, HM ;
HORVITZ, HR .
CELL, 1986, 44 (06) :817-829
[9]  
GOLSTEIN P, 1991, IMMUNOL REV, V121, P30
[10]   QUANTITATIVE INVITRO STUDIES ON NERVE GROWTH-FACTOR (NGF) REQUIREMENT OF NEURONS .1. SYMPATHETIC NEURONS [J].
GREENE, LA .
DEVELOPMENTAL BIOLOGY, 1977, 58 (01) :96-105