Cyclophosphamide enhances TNF-α-induced apoptotic cell death in murine vascular endothelial cell

被引:39
|
作者
Ohtani, T
Nakamura, T
Toda, K
Furukawa, F
机构
[1] Wakayama Med Coll, Dept Dermatol, Wakayama, Japan
[2] Kitano Hosp, Dept Dermatol, Osaka, Japan
来源
FEBS LETTERS | 2006年 / 580卷 / 06期
关键词
cyclophosphamide; TNF alpha; endothelial cell; caspase; bax;
D O I
10.1016/j.febslet.2006.01.092
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
Cyclophosphamide (CPA) is one of the therapeutic agents for systemic inflammatory disorders. In murine dermal endothelial cells (F-2), 4-hydroxycyclophosphamide (4-HC), which is active metabolite of CPA, enhanced TNF-alpha-induced DNA fragmentation. In addition, 4-HC was shown to elevate TNF-alpha-induced caspase-3 activation. Caspase-8 activation was identified by the treatment of TNF-alpha, whereas 4-HC was no effect. In contrast, only when treated with 4-HC, caspase-9 activation and the increase in the intracellular expression of Bax were detected. These results suggest that CPA may sensitize endothelial cells to TNF-alpha-induced apoptosis through a mitochondria-dependent pathway and clinically may contribute to the limitation of inflammatory process. (c) 2006 Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:1597 / 1600
页数:4
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