Nuclear apoptotic changes: An overview

被引:130
作者
Martelli, AM
Zweyer, M
Ochs, RL
Tazzari, PL
Tabellini, G
Narducci, P
Bortul, R
机构
[1] Univ Trieste, Dipartimento Morfol Umana Normale, I-34138 Trieste, Italy
[2] Univ Bologna, Sch Pharm, Dipartimento Sci Anat Umane & Fisiopatol Apparato, Sezione Anat Umana, I-40126 Bologna, Italy
[3] CNR, Ist Citomorfol Normale & Patol, I-40137 Bologna, Italy
[4] Precis Therapeut, Pittsburgh, PA 15213 USA
[5] St Orsola Marcello Malpighi Hosp, Serv Immunoematol & Trasfus, I-40138 Bologna, Italy
关键词
apoptosis; chromatin condensation; proteolysis; autoantibodies;
D O I
10.1002/jcb.1186
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
Apoptosis is a form of active cell death essential for morphogenesis, development, differentiation, and homeostasis of multicellular organisms. The activation of genetically controlled specific pathways that are highly conserved during evolution results in the characteristic morphological features of apoptosis that are mainly evident in the nucleus. These include chromatin condensation, nuclear shrinkage, and the formation of apoptotic bodies. The morphological changes are the result of molecular alterations, such as DNA and RNA cleavage, post-translational modifications of nuclear proteins, and proteolysis of several polypeptides residing in the nucleus. During the last five years our understanding of the process of apoptosis has dramatically increased. However, the mechanisms that lead to apoptotic changes in the nucleus have been only partially clarified. Here, we shall review the most recent findings that may explain why the nucleus displays these striking modifications. Moreover, we shall take into consideration the emerging evidence about apoptotic events as a trigger for the generation of autoantibodies to nuclear components. (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:634 / 646
页数:13
相关论文
共 107 条
[41]   A potential role of nuclear matrix-associated protein kinase CK2 in protection against drug-induced apoptosis in cancer cells [J].
Guo, CH ;
Yu, SH ;
Davis, AT ;
Wang, HM ;
Green, JE ;
Ahmed, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (08) :5992-5999
[42]   Segregation of RNA and separate packaging of DNA and RNA in apoptotic bodies during apoptosis [J].
Halicka, HD ;
Bedner, E ;
Darzynkiewicz, Z .
EXPERIMENTAL CELL RESEARCH, 2000, 260 (02) :248-256
[43]   The biochemistry of apoptosis [J].
Hengartner, MO .
NATURE, 2000, 407 (6805) :770-776
[44]   Caspases are activated in a branched protease cascade and control distinct downstream processes in Fas-induced apoptosis [J].
Hirata, H ;
Takahashi, A ;
Kobayashi, S ;
Yonehara, S ;
Sawai, H ;
Okazaki, T ;
Yamamoto, K ;
Sasada, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (04) :587-600
[45]  
Hughes JH, 1999, AM J CLIN PATHOL, V111, P267
[46]   Activation of a nuclear sphingomyelinase in radiation-induced apoptosis [J].
Jafrézou, JP ;
Bruno, AP ;
Moisand, A ;
Levade, T ;
Laurent, G .
FASEB JOURNAL, 2001, 15 (01) :123-133
[47]  
Jahr S, 2001, CANCER RES, V61, P1659
[48]   Caspase-3 is required for DNA fragmentation and morphological changes associated with apoptosis [J].
Jänicke, RU ;
Sprengart, ML ;
Wati, MR ;
Porter, AG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (16) :9357-9360
[49]   Noncaspase proteases in apoptosis [J].
Johnson, DE .
LEUKEMIA, 2000, 14 (09) :1695-1703
[50]  
Johnson VL, 2000, J CELL SCI, V113, P2941