Magnoliae flos induces apoptosis of RBL-2H3 cells via mitochondria and caspase

被引:21
|
作者
Kim, GC
Lee, SG
Park, BS
Kim, JY
Song, YS
Kim, JM
Yoo, KS
Huh, GY
Jeong, MH
Lim, YJ
Kim, HM
Yoo, YH
机构
[1] Dong A Univ, Coll Med, Dept Cell Biol & Anat, Program BK21, Pusan 602714, South Korea
[2] Busan Natl Univ, Coll Dent, Dept Oral Anat & Cell Biol, Pusan, South Korea
[3] Dong A Univ, Coll Med, Dept Pathol, Pusan 602714, South Korea
[4] Dong A Univ, Coll Med, Dept Microbiol & Immunol, Pusan 602714, South Korea
[5] Dong A Univ, Coll Med, Dept Parasitol, Pusan 602714, South Korea
[6] Inst Med Sci, Pusan, South Korea
[7] Kyung Hee Univ, Dept Pharmacol, Coll Oriental Med, Seoul, South Korea
关键词
magnoliae flos; apoptosis; mast cell; mitochondria; caspase;
D O I
10.1159/000070925
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Magnoliae flores (MF), the buds of Magnolia denudata Desrousseaux, have been successfully used for the management of allergic diseases in Korea. The purpose of the present study was to determine their causal role in inducing apoptosis of mast cells and to verify the underlying mechanism. Methods: The viability of mast cells was assessed by the trypan blue exclusion test. Induction of apoptosis was confirmed by DNA fragmentation, nuclear staining and DNA hypoploidy. Western blotting and immunofluorescent staining were performed to study the alterations in expression level and translocation of apoptosis-related proteins. Mitochondrial membrane potential (MMP) change and cytochrome C release were assayed. Results: We present several lines of evidence indicating that MF induce apoptosis. Changes in cell morphology, generation of DNA fragmentation, cell cycle arrest, activation of caspase-3, and PARP and DFF degradations were demonstrated. The reduction of MMP and the release of cytochrome C to cytosol were also shown. Either PTP blockers, bongkrekic acid and cyclosporin A, or pancaspase inhibitors, Boc.D-fmk and zVAD-fmk, did not prevent the release of cytochrome C. Bax protein content was increased, and Bax was translocated from cytosol into mitochondria at early time points after MF treatment. Conclusions: We have demonstrated that MF induce mitochondria- and caspase-dependent mast cell apoptosis. Our observations contribute new insights to the role of MF and support the view that the clinical effect of MF may depend on their pharmacological efficacy in regulating mast cell apoptosis. Copyright (C) 2003 S. Karger AG, Basel.
引用
收藏
页码:101 / 110
页数:10
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