Selenite-induced apoptosis of osteoclasts mediated by the mitochondrial pathway

被引:52
作者
Chung, YW
Kim, TS
Lee, SY
Lee, SH
Choi, Y
Kim, N
Min, BM
Jeong, DW
Kim, IY [1 ]
机构
[1] Korea Univ, Sdch Life Sci & Biotechnol, Lab Cellular & Mol Biochem, Seoul 136701, South Korea
[2] Ewha Womans Univ, Div Mol Life Sci, Seoul 120750, South Korea
[3] Ewha Womans Univ, Ctr Cell Signaling Res, Seoul 120750, South Korea
[4] Univ Penn, Abramson Canc Res Inst, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[5] Chonnam Natl Univ, Sch Med, Med Res Ctr Gene Regulat, Kwangju, South Korea
[6] Seoul Natl Univ, Coll Dent, Inst Dent Res, Dept Oral Biochem, Seoul, South Korea
[7] Seoul Natl Univ, Coll Dent, Inst Dent Res, Sect Craniofacial Reconstruct, Seoul, South Korea
[8] Seoul Natl Univ, Human Life Sci BK21, Seoul, South Korea
关键词
selenium; apoptosis; osteoclast; mitochondria;
D O I
10.1016/j.toxlet.2005.06.019
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 [卫生毒理学];
摘要
The possible effects of sodium selenite on mature osteoclasts were investigated. Incubation of osteoclast-like cells differentiated from RAW 264.7 cells with sodium selenite induced apoptosis as revealed by morphological changes, internucleosomal DNA fragmentation, and activation of caspase-3. Selenite also induced generation of the superoxide anion and reduced the number of free thiol groups in the osteoclast-like cells, suggestive of a shift to a more oxidizing intracellular environment. In addition, selenite induced protein aggregation by thiol cross-linking, loss of the mitochondrial membrane potential, and cytochrome c release in mitochondria isolated from the osteoclast-like cells. Finally, selenite-induced DNA fragmentation in osteoclasts was inhibited both by cyclosporin A, a blocker of the mitochondrial permeability transition pore, and by DEVD-CHO, a cell-permeable inhibitor of caspase-3. These results thus suggest that selenite induces apoprosis mediated by the mitochondrial pathway in mature osteoclasts. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:143 / 150
页数:8
相关论文
共 49 条
[1]
Selective toxic effects of tamoxifen on osteoclasts: Comparison with the effects of oestrogen [J].
Arnett, TR ;
Lindsay, R ;
Kilb, JM ;
Moonga, BS ;
Spowage, M ;
Dempster, DW .
JOURNAL OF ENDOCRINOLOGY, 1996, 149 (03) :503-508
[2]
Osteoclast differentiation and activation [J].
Boyle, WJ ;
Simonet, WS ;
Lacey, DL .
NATURE, 2003, 423 (6937) :337-342
[3]
Selenium compounds prevent the induction of drug resistance by cisplatin in human ovarian tumor xenografts in vivo [J].
Caffrey, PB ;
Frenkel, GD .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2000, 46 (01) :74-78
[4]
Evaluation of nutritional status and pathophysiology of growth retardation in patients with phenylketonuria [J].
Dobbelaere, D ;
Michaud, L ;
Debrabander, A ;
Vanderbecken, S ;
Gottrand, F ;
Turck, D ;
Farriaux, JP .
JOURNAL OF INHERITED METABOLIC DISEASE, 2003, 26 (01) :1-11
[5]
THE REFINED STRUCTURE OF THE SELENOENZYME GLUTATHIONE-PEROXIDASE AT 0.2-NM RESOLUTION [J].
EPP, O ;
LADENSTEIN, R ;
WENDEL, A .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1983, 133 (01) :51-69
[6]
FAGIAN MM, 1990, J BIOL CHEM, V265, P19955
[7]
Bisphosphonates: Preclinical aspects and use in osteoporosis [J].
Fleisch, HA .
ANNALS OF MEDICINE, 1997, 29 (01) :55-62
[8]
Selenium metabolism, selenoproteins and mechanisms of cancer prevention: complexities with thioredoxin reductase [J].
Ganther, HE .
CARCINOGENESIS, 1999, 20 (09) :1657-1666
[9]
Mitochondria and apoptosis [J].
Green, DR ;
Reed, JC .
SCIENCE, 1998, 281 (5381) :1309-1312
[10]
Caspases:: key players in programmed cell death [J].
Grütter, MG .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 2000, 10 (06) :649-655