Co-clustering of Golgi complex and other cytoplasmic organelles to crescentic region of half-moon nuclei during apoptosis

被引:9
作者
Nozawa, Kazuhisa [1 ,2 ]
Fritzler, Marvin J. [4 ]
Takasaki, Yoshinari [3 ,4 ]
Wood, Malcolm R. [5 ]
Chan, Edward K. L. [2 ]
机构
[1] Juntendo Univ, Grad Sch Med, Dept Rheumatol & Internal Med, Urayasu Hosp,Inst Environm & Gender Specif Med, Chiba, Japan
[2] Univ Florida, Dept Oral Biol, Gainesville, FL 32610 USA
[3] Juntendo Univ, Sch Med, Dept Rheumatol, Tokyo 113, Japan
[4] Univ Calgary, Dept Biochem & Mol Biol, Calgary, AB, Canada
[5] Scripps Res Inst, Core Microscopy Facil, La Jolla, CA 92037 USA
基金
美国国家卫生研究院;
关键词
Apoptosis; Golgi complex; Staurosporine; MITOCHONDRIAL PERMEABILITY TRANSITION; GD3; GANGLIOSIDE; MOLECULAR CHARACTERIZATION; CELL-DEATH; MEMBRANE; FRAGMENTATION; ACIDIFICATION; AUTOANTIGENS; CASPASE-2; APPARATUS;
D O I
10.1016/j.cellbi.2008.10.016
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Early apoptosis is defined by stereotypic morphological changes, especially evident in the nucleus, where chromatin condenses and compacts, and assumes a globular, half-moon or crescent-shaped morphology. Accumulating evidence suggests that cytoplasmic organelles such as mitochondria and the Golgi complex are major sites of integration of pro-apoptotic signaling. In this study, cytoplasmic organelles including Golgi complex, mitochondria, endosomes, lysosomes, and peroxisomes were shown to condense at the same unique region adjacent to the crescentic nucleus during a relatively early stage of apoptosis induced by staurosporine or other agents. The co-clustering phenomenon may be caused by shrinkage of cytoplasm during apoptosis although cytoskeletal markers actin and tubulin were not condensed and appeared excluded. These data suggest the co-clustering of cytoplasmic organelles plays an interesting role during the progression of the apoptotic process. It is possible that modification of pro-apoptotic proteins may arise as a result of the interplay of these cytoplasmic organelles. (C) 2008 International Federation for Cell Biology. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:148 / 157
页数:10
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