A measure of the mitotic index:: studies of the abundance and half-life of p34cdc2 in cultured cells and normal and neoplastic tissues

被引:16
作者
Gannon, JV
Nebreda, A
Goodger, NM
Morgan, PR
Hunt, T
机构
[1] ICRF Labs, S Mimms EN6 3LD, Herts, England
[2] UMDS, Dept Oral Med & Pathol, London SE1 9RT, England
关键词
D O I
10.1046/j.1365-2443.1998.00163.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background: The cdc2 gene encodes a protein kinase, p34(cdc2), that is essential for mitosis, and is present at high levels in dividing cells. Classical studies of the levels of this protein in dividing and resting cells used antibodies that cross-react with other members of the CDK family, in particular with CDK2. We have therefore re-examined the abundance of p34(cdc2) in a variety of tissues and cell lines, using a highly specific, epitope-mapped monoclonal antibody that does not react with CDK2. Results: We observed high levels of p34(cdc2) in proliferating cells, especially those in neoplastic tissues, Cells that have withdrawn from the cell cycle have low or undetectable levels, At the end of mitosis, che level of p34(cdc2) declines, with simple first-order kinetics, with a half-life which is never less than 6h and is more typically about 18h. The persistence of p34(cdc2) after the last cell division is comparable to that of PCNA, a commonly used marker of proliferation. Conclusions: The immunochemical detection of p34(cdc2) provides an accurate, reliable and meaningful measure of the proliferative activity of cells in tissues, We suggest that p34(cdc2) should be considered as the most authentic molecular marker of the mitotic index.
引用
收藏
页码:17 / 27
页数:11
相关论文
共 70 条
[1]   DETECTION OF NUCLEOTIDE EXCISION-REPAIR INCISIONS IN HUMAN FIBROBLASTS BY IMMUNOSTAINING FOR PCNA [J].
ABOUSSEKHRA, A ;
WOOD, RD .
EXPERIMENTAL CELL RESEARCH, 1995, 221 (02) :326-332
[2]   INVESTIGATION OF THE ROLE OF G(1)/S CELL-CYCLE MEDIATORS IN CELLULAR SENESCENCE [J].
AFSHARI, CA ;
VOJTA, PJ ;
ANNAB, LA ;
FUTREAL, PA ;
WILLARD, TB ;
BARRETT, JC .
EXPERIMENTAL CELL RESEARCH, 1993, 209 (02) :231-237
[3]   INTRACELLULAR-LOCALIZATION AND EXPRESSION OF MAMMALIAN CDC2 PROTEIN DURING MYOGENIC DIFFERENTIATION [J].
AKHURST, RJ ;
FLAVIN, NB ;
WORDEN, J ;
LEE, MG .
DIFFERENTIATION, 1989, 40 (01) :36-41
[4]  
[Anonymous], 1988, Antibodies: A Laboratory Manual
[5]  
BAILLY E, 1992, J CELL SCI, V101, P529
[6]  
BARTEK J, 1993, STEM CELLS DAYT, V1, P51
[7]   C-MYC COOPERATES WITH ACTIVATED RAS TO INDUCE THE CDC2 PROMOTER [J].
BORN, TL ;
FROST, JA ;
SCHONTHAL, A ;
PRENDERGAST, GC ;
FERAMISCO, JR .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (09) :5710-5718
[8]   EXISTENCE OF 2 POPULATIONS OF CYCLIN PROLIFERATING CELL NUCLEAR ANTIGEN DURING THE CELL-CYCLE - ASSOCIATION WITH DNA-REPLICATION SITES [J].
BRAVO, R ;
MACDONALDBRAVO, H .
JOURNAL OF CELL BIOLOGY, 1987, 105 (04) :1549-1554
[9]   INDUCTION OF A-TYPE AND D-TYPE CYCLINS AND CDC2 KINASE-ACTIVITY DURING RECOVERY FROM SHORT-TERM HYPEROXIC LUNG INJURY [J].
BUI, KC ;
BUCKLEY, S ;
WU, F ;
UHAL, B ;
JOSHI, I ;
LIU, JA ;
HUSSAIN, M ;
MAKHOUL, I ;
WARBURTON, D .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1995, 268 (04) :L625-L635
[10]   CELL-CYCLE DEPENDENT REGULATION OF CDC2 MESSENGER-RNA IN MOUSE FIBROBLASTS - REQUIREMENT OF PROTEIN-SYNTHESIS AND OF CONTINUED MITOGENIC STIMULATION [J].
BUQUETFAGOT, C ;
FAGOT, D ;
MESTER, J .
JOURNAL OF CELLULAR PHYSIOLOGY, 1993, 155 (01) :204-209