Normal and c-Myc-promoted human keratinocyte differentiation both occur via a novel cell cycle involving cellular growth and endoreplication

被引:70
作者
Gandarillas, A [1 ]
Davies, D
Blanchard, JM
机构
[1] CNRS, Inst Genet Mol, F-34293 Montpellier 5, France
[2] Imperial Canc Res Fund, FACS Lab, London WC2A 3PX, England
关键词
epidermis; mitosis; cell size; flow cytometry; cell fate; endoreduplication;
D O I
10.1038/sj.onc.1203630
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
The relationship between cell cycle and differentiation in human keratinocytes is poorly understood, It is believed that keratinocytes suppress DNA replication and cell cycle arrest in G0 before they initiate terminal differentiation, However, a temporal separation between both events has not been established. Moreover, c-Myc promotes keratinocyte differentiation without causing cell cycle arrest. To address these paradoxes we have analysed cell cycle control during normal and c-Myc-promoted differentiation. Continuous activation of c-Myc or initiation of terminal differentiation results in a block of G2/M, cellular growth, endoreplication and polyploidy. Keratinocytes abandon G1, continue replicating DNA as they differentiate terminally and become polyploid. In fact, simply blocking mitosis with nocodazole resulted in increased cell size, terminal differentiation and endoreplication. This indicates that terminal differentiation associates with defective cell cycle progression and provides a novel insight into c-Myc biology.
引用
收藏
页码:3278 / 3289
页数:12
相关论文
共 67 条
[1]   FIBRONECTIN INHIBITS THE TERMINAL DIFFERENTIATION OF HUMAN KERATINOCYTES [J].
ADAMS, JC ;
WATT, FM .
NATURE, 1989, 340 (6231) :307-309
[2]  
Amati Bruno, 1998, Frontiers in Bioscience, V3, pD250
[3]   INVOLUCRIN SYNTHESIS AND TISSUE ASSEMBLY BY KERATINOCYTES IN NATURAL AND CULTURED HUMAN EPITHELIA [J].
BANKSSCHLEGEL, S ;
GREEN, H .
JOURNAL OF CELL BIOLOGY, 1981, 90 (03) :732-737
[4]   FLOW CYTOMETRIC IDENTIFICATION OF PROLIFERATIVE SUBPOPULATIONS WITHIN NORMAL HUMAN EPIDERMIS AND THE LOCALIZATION OF THE PRIMARY HYPERPROLIFERATIVE POPULATION IN PSORIASIS [J].
BATACSORGO, Z ;
HAMMERBERG, C ;
VOORHEES, JJ ;
COOPER, KD .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (04) :1271-1281
[5]  
BenBassat H, 1997, CANCER RES, V57, P3741
[6]   Cellular control lies in the balance of forces [J].
Chicurel, ME ;
Chen, CS ;
Ingber, DE .
CURRENT OPINION IN CELL BIOLOGY, 1998, 10 (02) :232-239
[7]   Size control in animal development [J].
Conlon, I ;
Raff, M .
CELL, 1999, 96 (02) :235-244
[8]  
Dang CV, 1999, MOL CELL BIOL, V19, P1
[9]   Inhibitory function of p21Cip1/WAF1 in differentiation of primary mouse keratinocytes independent of cell cycle control [J].
Di Cunto, F ;
Topley, G ;
Calautti, E ;
Hsiao, J ;
Ong, L ;
Seth, PK ;
Dotto, GP .
SCIENCE, 1998, 280 (5366) :1069-1072
[10]   MEASUREMENT OF THE RATE OF EPIDERMAL TERMINAL DIFFERENTIATION - EXPRESSION OF INVOLUCRIN BY S-PHASE KERATINOCYTES IN CULTURE AND IN PSORIATIC PLAQUES [J].
DOVER, R ;
WATT, FM .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1987, 89 (04) :349-352