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
[51]  
Paramio JM, 1999, MOL CELL BIOL, V19, P3086
[52]   Reversible activation of c-Myc in skin: Induction of a complex neoplastic phenotype by a single oncogenic lesion [J].
Pelengaris, S ;
Littlewood, T ;
Khan, M ;
Elia, G ;
Evan, G .
MOLECULAR CELL, 1999, 3 (05) :565-577
[53]   LOCATION OF PROLIFERATING CELLS IN HUMAN EPIDERMIS [J].
PENNEYS, NS ;
FULTON, JE ;
WEINSTEI.GD ;
FROST, P .
ARCHIVES OF DERMATOLOGY, 1970, 101 (03) :323-+
[54]   TGF-BETA-1 INHIBITION OF C-MYC TRANSCRIPTION AND GROWTH IN KERATINOCYTES IS ABROGATED BY VIRAL TRANSFORMING PROTEINS WITH PRB BINDING DOMAINS [J].
PIETENPOL, JA ;
STEIN, RW ;
MORAN, E ;
YACIUK, P ;
SCHLEGEL, R ;
LYONS, RM ;
PITTELKOW, MR ;
MUNGER, K ;
HOWLEY, PM ;
MOSES, HL .
CELL, 1990, 61 (05) :777-785
[55]   DIRECTION OF MITOTIC AXIS IN HUMAN EPIDERMIS [J].
PINKUS, H ;
HUNTER, R .
ARCHIVES OF DERMATOLOGY, 1966, 94 (03) :351-&
[56]   ONSET OF EPIDERMAL DIFFERENTIATION IN RAPIDLY PROLIFERATING BASAL KERATINOCYTES [J].
REGNIER, M ;
VAIGOT, P ;
DARMON, M ;
PRUNIERAS, M .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1986, 87 (04) :472-476
[57]  
REISS M, 1987, CANCER RES, V47, P6705
[58]  
Rheinwald JG, 1989, Cell Growth and Division, P81
[59]   Control of cell growth by c-Myc in the absence of cell division [J].
Schuhmacher, M ;
Staege, MS ;
Pajic, A ;
Polack, A ;
Weidle, UH ;
Bornkamm, GW ;
Eick, D ;
Kohlhuber, F .
CURRENT BIOLOGY, 1999, 9 (21) :1255-1258
[60]  
Solari F, 1996, J CELL SCI, V109, P1203