Specific down-regulation of annexin II expression in human cells interferes with cell proliferation

被引:85
作者
Chiang, YP
Rizzino, A
Sibenaller, ZA
Wold, MS
Vishwanatha, JK
机构
[1] Univ Nebraska, Med Ctr, Dept Biochem & Mol Biol, Omaha, NE 68198 USA
[2] Univ Nebraska, Med Ctr, Eppley Inst Res Canc & Allied Dis, Omaha, NE 68198 USA
[3] Univ Iowa, Coll Med, Dept Biochem, Iowa City, IA 52242 USA
关键词
annexin II; DNA synthesis; antisense; Simian Virus 40; cell proliferation;
D O I
10.1023/A:1006942128672
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The protein-tyrosine kinase substrate annexin II is a growth regulated gene whose expression is increased in several human cancers. While the precise function of this protein is not understood, annexin II is proposed to be involved in multiple physiological activities, including DNA synthesis and cell proliferation. Targeted disruption of the annexin II gene affects calcium signaling, tyrosine phosphorylation and apoptosis, indicating the important physiological role of this protein. We used a transient co-transfection assay to regulate annexin II expression in human HeLa, 293 and 293T cells, and measured the effects of annexin II down regulation on DNA synthesis and proliferation. Transfection of cells with an antisense annexin II vector results in inhibition of cell division and proliferation, with concomitant reduction in annexin II message and protein levels. Cellular DNA synthesis is significantly reduced in antisense transfected cells. Replication extracts made from antisense transfected cells have significantly reduced efficiency to support SV40 in vitro DNA replication, while the extracts made from sense transfected cells are fully capable of replication. Our results indicate an important role of annexin II in cellular DNA synthesis and cell proliferation.
引用
收藏
页码:139 / 147
页数:9
相关论文
共 30 条
[1]  
CHIANG YP, 1993, CANCER RES, V53, P6017
[2]   ELEVATED EXPRESSION OF ANNEXIN-II (LIPOCORTIN-II, P36) IN A MULTIDRUG RESISTANT SMALL-CELL LUNG-CANCER CELL-LINE [J].
COLE, SPC ;
PINKOSKI, MJ ;
BHARDWAJ, G ;
DEELEY, RG .
BRITISH JOURNAL OF CANCER, 1992, 65 (04) :498-502
[3]   TRANSCRIPTIONAL AND POSTTRANSCRIPTIONAL REGULATION OF INTERFERON-INDUCED GENE-EXPRESSION IN HUMAN-CELLS [J].
FRIEDMAN, RL ;
MANLY, SP ;
MCMAHON, M ;
KERR, IM ;
STARK, GR .
CELL, 1984, 38 (03) :745-755
[4]   ENHANCED EXPRESSION OF THE PROTEIN-KINASE SUBSTRATE P36 IN HUMAN HEPATOCELLULAR-CARCINOMA [J].
FROHLICH, M ;
MOTTE, P ;
GALVIN, K ;
TAKAHASHI, H ;
WANDS, J ;
OZTURK, M .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (06) :3216-3223
[5]   INHIBITION OF CELL-PROLIFERATION BY C/EBP-ALPHA OCCURS IN MANY CELL-TYPES, DOES NOT REQUIRE THE PRESENCE OF P53 OR RB, AND IS NOT AFFECTED BY LARGE T-ANTIGEN [J].
HENDRICKSTAYLOR, LR ;
DARLINGTON, GJ .
NUCLEIC ACIDS RESEARCH, 1995, 23 (22) :4726-4733
[6]  
HENRICKSEN LA, 1994, J BIOL CHEM, V269, P11121
[7]  
JINDAL HK, 1991, J BIOL CHEM, V266, P5169
[8]   PURIFICATION AND CHARACTERIZATION OF PRIMER RECOGNITION PROTEINS FROM HELA-CELLS [J].
JINDAL, HK ;
VISHWANATHA, JK .
BIOCHEMISTRY, 1990, 29 (20) :4767-4773
[9]   THE GROWTH-REGULATED GENE 1B6 IS IDENTIFIED AS THE HEAVY-CHAIN OF CALPACTIN-I [J].
KEUTZER, JC ;
HIRSCHHORN, RR .
EXPERIMENTAL CELL RESEARCH, 1990, 188 (01) :153-159
[10]   CA-2+-DEPENDENT PHOSPHOLIPID-BINDING (AND MEMBRANE-BINDING) PROTEINS [J].
KLEE, CB .
BIOCHEMISTRY, 1988, 27 (18) :6645-6653