UV-induced apoptosis in resistant HeLa cells

被引:19
作者
Kamarajan, P [1 ]
Chao, CCK [1 ]
机构
[1] Chang Gung Univ, Dept Biochem, Tumor Biol Lab, Tao Yuan 33332, Taiwan
关键词
apoptosis; DNA repair; UV-resistance; HeLa;
D O I
10.1023/A:1005515400285
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
Recently, apoptosis (genetically programmed cell death) induced by UV has been documented in some cell culture models. However, the significance of apoptosis in W-induced cytotoxicity and resistance is uncertain. In this study, we investigated the induction of apoptosis in HeLa cells and its role in acquired UV-resistance. The membrane receptor Fas was induced to assembly, and its immediate downstream target, caspase-8, was induced by UV in a dose- and time-dependent manner. Caspase-10, another possible candidate for forming the death-inducing signaling complex with Fas, was also activated in a dose- and time-dependent manner. There was significant activation of caspase 9, 3 and 2 by UV. The apoptotic pathways appeared to be normal in acquired UV-resistant HeLa cells. In addition,. there was a UV dose-dependent induction of chromatin condensation in both parental and UV-resistant cells. However, resistant cells displayed significant reduction in chromatin condensation at lower doses. Inhibition of caspase-3 activation by specific inhibitor significantly reduced the chromatin condensation in both cell types, and unexpectedly, the difference between the two cell lines was completely eradicated, suggesting that the caspase-3 pathway plays a significant role in reducing apoptosis in resistant cells. The results indicate that UV induces apoptosis by direct activation of apoptotic proteins in HeLa and resistant cells. Although resistant cells displayed partial inhibition of W-induced apoptosis through the caspase-3 pathway, there was no consistent difference in the activation of this and related caspase-9 caspases compared to parental HeLa cells.
引用
收藏
页码:99 / 108
页数:10
相关论文
共 33 条
[1]   Apaf1 (CED-4 homolog) regulates programmed cell death in mammalian development [J].
Cecconi, F ;
Alvarez-Bolado, G ;
Meyer, BI ;
Roth, KA ;
Gruss, P .
CELL, 1998, 94 (06) :727-737
[2]  
CHAO CCK, 1991, CANCER RES, V51, P601
[3]   APPARENT ALTERATIONS IN THE EARLY-STAGE OF EXCISION-REPAIR OF UV-INDUCED DNA DAMAGES IN A HELA MUTANT-CELL LINE THAT IS RESISTANT TO GENOTOXIC STRESSES [J].
CHAO, CCK ;
HUANG, SL .
MUTATION RESEARCH, 1993, 303 (01) :19-27
[4]   CROSS-RESISTANCE TO UV-RADIATION OF A CISPLATIN-RESISTANT HUMAN CELL-LINE - OVEREXPRESSION OF CELLULAR FACTORS THAT RECOGNIZE UV-MODIFIED DNA [J].
CHAO, CCK ;
HUANG, SL ;
HUANG, HM ;
LINCHAO, S .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (04) :2075-2080
[5]   Caspases: the executioners of apoptosis [J].
Cohen, GM .
BIOCHEMICAL JOURNAL, 1997, 326 :1-16
[6]   A caspase-activated DNase that degrades DNA during apoptosis, and its inhibitor ICAD [J].
Enari, M ;
Sakahira, H ;
Yokoyama, H ;
Okawa, K ;
Iwamatsu, A ;
Nagata, S .
NATURE, 1998, 391 (6662) :43-50
[7]   Sequential activation of ICE-like and CPP32-like proteases during Fas-mediated apoptosis [J].
Enari, M ;
Talanian, RV ;
Wong, WW ;
Nagata, S .
NATURE, 1996, 380 (6576) :723-726
[8]   Differential requirement for Caspase 9 in apoptotic pathways in vivo [J].
Hakem, R ;
Hakem, A ;
Duncan, GS ;
Henderson, JT ;
Woo, M ;
Soengas, MS ;
Elia, A ;
de la Pompa, JL ;
Kagi, D ;
Khoo, W ;
Potter, J ;
Yoshida, R ;
Kaufman, SA ;
Lowe, SW ;
Penninger, JM ;
Mak, TW .
CELL, 1998, 94 (03) :339-352
[9]   CYTOTOXICITY-DEPENDENT APO-1 (FAS/CD95)-ASSOCIATED PROTEINS FORM A DEATH-INDUCING SIGNALING COMPLEX (DISC) WITH THE RECEPTOR [J].
KISCHKEL, FC ;
HELLBARDT, S ;
BEHRMANN, I ;
GERMER, M ;
PAWLITA, M ;
KRAMMER, PH ;
PETER, ME .
EMBO JOURNAL, 1995, 14 (22) :5579-5588
[10]   Reduced apoptosis and cytochrome c-mediated caspase activation in mice lacking Caspase 9 [J].
Kuida, K ;
Haydar, TF ;
Kuan, CY ;
Gu, Y ;
Taya, C ;
Karasuyama, H ;
Su, MSS ;
Rakic, P ;
Flavell, RA .
CELL, 1998, 94 (03) :325-337