The sensitizer 2,4-dinitrofluorobenzene activates caspase-3 and induces cell death in a skin dendritic cell line

被引:10
作者
Cruz, MT
Duarte, CB
Gonçalo, M
Figueiredo, A
Carvalho, AP
Lopes, MC
机构
[1] Univ Coimbra, Fac Farm, P-3000295 Coimbra, Portugal
[2] Univ Coimbra, Ctr Neurociencias, Coimbra, Portugal
[3] Hosp Univ Coimbra, Fac Med, Dermatol Serv, Coimbra, Portugal
关键词
apoptosis; caspase-3; cell death; DCNB; dendritic cells; DNFB;
D O I
10.1080/10915810305069
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In this work, a dendritic cell line derived from mouse skin (FSDC) was used, as an in vitro experimental model, to evaluate the cytotoxic effect of two chemical sensitizers, a strong sensitizer (2,4-dinitrofluorobenzene, DNFB) and a weak sensitizer (2,4-dichloronitrobenzene, DCNB). The results indicated that DNFB reduces the cellular metabolism of FSDC, as evaluated by the reduction of the tetrazolium salt, 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT). All the DNFB concentrations tested, ranging from 5.2 muM to 26 muM, significantly inhibited the MTT reduction after 1 hour of cell exposure to the sensitizer. In contrast, incubation of FSDC with the weak sensitizer DCNB had no significant effect on the MTT reduction assay. When the cells were incubated with DNFB (13 muM), for 3 and 6 hours, morphological changes characteristics of cell death by apoptosis were observed, as assessed by propidium iodide (PI) DNA staining and annexin-V externalization analysis. These results correlate well with an increase of caspase-3-like activity after FSDC exposure to DNFB (13 muM) for 6 hours. Together, these results indicate that apoptotic death of skin dendritic cells occurs after exposure to the sensitizer DNFB, although necrotic cell death was also observed when the cells were incubated with high concentrations of DNFB (26 muM), or after long periods of cell exposure to the chemical DNFB (13 muM, for 6 hours).
引用
收藏
页码:43 / 48
页数:6
相关论文
共 25 条
[1]   Dendritic cells differently respond to haptens and irritants by their production of cytokines and expression of co-stimulatory molecules [J].
Aiba, S ;
Terunuma, A ;
Manome, H ;
Tagami, H .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1997, 27 (11) :3031-3038
[2]   Dendritic cells and the control of immunity [J].
Banchereau, J ;
Steinman, RM .
NATURE, 1998, 392 (6673) :245-252
[3]   Dichloronitrobenzene: A reappraisal of its skin sensitization potential [J].
Basketter, DA ;
Scholes, EW ;
Fielding, I ;
Dearman, RJ ;
Hilton, J ;
Kimber, I .
CONTACT DERMATITIS, 1996, 34 (01) :55-58
[4]   Targeted antigen delivery to antigen-presenting cells including dendritic cells by engineered Fas-mediated apoptosis [J].
Chattergoon, MA ;
Kim, JJ ;
Yang, JS ;
Robinson, TM ;
Lee, DJ ;
Dentchev, T ;
Wilson, DM ;
Ayyavoo, V ;
Weiner, DB .
NATURE BIOTECHNOLOGY, 2000, 18 (09) :974-979
[5]   Caspases: the executioners of apoptosis [J].
Cohen, GM .
BIOCHEMICAL JOURNAL, 1997, 326 :1-16
[6]  
De Smedt T, 1998, J IMMUNOL, V161, P4476
[7]   Allergic contact dermatitis: understanding the immune response and potential for targeted therapy using cytokines [J].
Enk, AH .
MOLECULAR MEDICINE TODAY, 1997, 3 (10) :423-428
[8]   The most unkindest cut of all*: on the multiple roles of mammalian caspases [J].
Fadeel, B ;
Orrenius, S ;
Zhivotovsky, B .
LEUKEMIA, 2000, 14 (08) :1514-1525
[9]   The role of phosphatidylserine in recognition of apoptotic cells by phagocytes [J].
Fadok, VA ;
Bratton, DL ;
Frasch, SC ;
Warner, ML ;
Henson, PM .
CELL DEATH AND DIFFERENTIATION, 1998, 5 (07) :551-562
[10]   ESTABLISHMENT OF A CELL-LINE WITH FEATURES OF EARLY DENDRITIC CELL PRECURSORS FROM FETAL MOUSE SKIN [J].
GIROLOMONI, G ;
LUTZ, MB ;
PASTORE, S ;
ABMANN, CU ;
CAVANI, A ;
RICCIARDICASTAGNOLI, P .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1995, 25 (08) :2163-2169