HUMAN NEUTROPHIL PEPTIDE DEFENSINS INDUCE SINGLE-STRAND DNA BREAKS IN TARGET-CELLS

被引:56
|
作者
GERA, JF
LICHTENSTEIN, A
机构
[1] Department of Medicine, V. A. Wadsworth-UCLA Medical Center, Los Angeles
关键词
D O I
10.1016/0008-8749(91)90136-Y
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
To investigate whether target cell DNA injury participates in cytolysis by human neutrophil defensins (HNP), we analyzed HNP-treated cells for single strand breaks by the alkaline unwinding assay and the activation of ADPribose polymerase, a DNA repair enzyme. Strand breaks and ADP-ribosylation were first detected in K562 and Raji targets 6-8 hr after incubation with HNP and increased to maximal levels by 18 hr. DNA was not degraded into nucleosome-sized fragments. To assess the impact of DNA injury on cytolysis, we increased strand breakage by coincubating targets with HNP and two inhibitors of ADPribose polymerase, 3-aminobenzamide, or nicotin-amide. Concurrently with inhibiting polymerase activity and increasing DNA injury, these agents significantly enhanced HNP-mediated cytolysis. Enhancement occurred only at time points (over 6 hr) and in targets (only nucleated targets) where HNP-induced DNA injury could be occurring. These data indicate that neutrophil defensins can induce DNA injury in targets and suggest such injury may be involved in target cell death. © 1991.
引用
收藏
页码:108 / 120
页数:13
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