The modular systems biology approach to investigate the control of apoptosis in Alzheimer's disease neurodegeneration

被引:41
作者
Alberghina, Lilia [1 ]
Colangelo, Anna Maria [1 ]
机构
[1] Univ Milano Bicocca, Lab Neurosci R Levi Montalcini, Dept Biotechnol & Biosci, I-20126 Milan, Italy
关键词
Nerve Growth Factor; Mild Cognitive Impairment; Neuronal Apoptosis; Cell Cycle Event; Cell Cycle Reentry;
D O I
10.1186/1471-2202-7-S1-S2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Apoptosis is a programmed cell death that plays a critical role during the development of the nervous system and in many chronic neurodegenerative diseases, including Alzheimer's disease (AD). This pathology, characterized by a progressive degeneration of cholinergic function resulting in a remarkable cognitive decline, is the most common form of dementia with high social and economic impact. Current therapies of AD are only symptomatic, therefore the need to elucidate the mechanisms underlying the onset and progression of the disease is surely needed in order to develop effective pharmacological therapies. Because of its pivotal role in neuronal cell death, apoptosis has been considered one of the most appealing therapeutic targets, however, due to the complexity of the molecular mechanisms involving the various triggering events and the many signaling cascades leading to cell death, a comprehensive understanding of this process is still lacking. Modular systems biology is a very effective strategy in organizing information about complex biological processes and deriving modular and mathematical models that greatly simplify the identification of key steps of a given process. This review aims at describing the main steps underlying the strategy of modular systems biology and briefly summarizes how this approach has been successfully applied for cell cycle studies. Moreover, after giving an overview of the many molecular mechanisms underlying apoptosis in AD, we present both a modular and a molecular model of neuronal apoptosis that suggest new insights on neuroprotection for this disease.
引用
收藏
页数:26
相关论文
共 233 条
[11]   GLUTAMATE-INDUCED NEURONAL DEATH - A SUCCESSION OF NECROSIS OR APOPTOSIS DEPENDING ON MITOCHONDRIAL-FUNCTION [J].
ANKARCRONA, M ;
DYPBUKT, JM ;
BONFOCO, E ;
ZHIVOTOVSKY, B ;
ORRENIUS, S ;
LIPTON, SA ;
NICOTERA, P .
NEURON, 1995, 15 (04) :961-973
[12]   Neuronal expression of cycline dependent kinase inhibitors of the INK4 family in Alzheimer's disease [J].
Arendt, T ;
Holzer, M ;
Gärtner, U .
JOURNAL OF NEURAL TRANSMISSION, 1998, 105 (8-9) :949-960
[13]   Interleukin-10 prevents glutamate-mediated cerebellar granule cell death by blocking caspase-3-like activity [J].
Bachis, A ;
Colangelo, AM ;
Vicini, S ;
Doe, PP ;
De Bernardi, MA ;
Brooker, G ;
Mocchetti, I .
JOURNAL OF NEUROSCIENCE, 2001, 21 (09) :3104-3112
[14]   Interaction of Tau with Fe65 links tau to APP [J].
Barbato, C ;
Canu, N ;
Zambrano, N ;
Serafino, A ;
Minopoli, G ;
Ciotti, MT ;
Amadoro, G ;
Russo, T ;
Calissano, P .
NEUROBIOLOGY OF DISEASE, 2005, 18 (02) :399-408
[15]   CK2 regulates in vitro the activity of the yeast cyclin-dependent kinase inhibitor Sic1 [J].
Barberis, M ;
Pagano, MA ;
De Gioia, L ;
Marin, O ;
Vanoni, M ;
Pinna, LA ;
Alberghina, L .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 336 (04) :1040-1048
[16]   The yeast cyclin-dependent kinase inhibitor Sic1 and mammalian p27Kip1 are functional homologues with a structurally conserved inhibitory domain [J].
Barberis, M ;
De Gioia, L ;
Ruzzene, M ;
Sarno, S ;
Coccetti, P ;
Fantucci, P ;
Vanoni, M ;
Alberghina, L .
BIOCHEMICAL JOURNAL, 2005, 387 :639-647
[17]   ProNGF induces p75-mediated death of oligodendrocytes following spinal cord injury [J].
Beattie, MS ;
Harrington, AW ;
Lee, R ;
Kim, JY ;
Boyce, SL ;
Longo, FM ;
Bresnahan, JC ;
Hempstead, BL ;
Yoon, SO .
NEURON, 2002, 36 (03) :375-386
[18]   'The stress of ding': the role of heat shock proteins in the regulation of apoptosis [J].
Beere, HM .
JOURNAL OF CELL SCIENCE, 2004, 117 (13) :2641-2651
[19]   Mathematical modeling reveals threshold mechanism in CD95-induced apoptosis [J].
Bentele, M ;
Lavrik, I ;
Ulrich, M ;
Stösser, S ;
Heermann, DW ;
Kalthoff, H ;
Krammer, PH ;
Eils, R .
JOURNAL OF CELL BIOLOGY, 2004, 166 (06) :839-851
[20]   Interactions between GSK3β and caspase signalling pathways during NGF deprivation induced cell death [J].
Bhat, Ratan, V ;
Leonov, Sergey ;
Luthman, Johan ;
Scott, Clay W. ;
Lee, Chi-Ming .
JOURNAL OF ALZHEIMERS DISEASE, 2002, 4 (04) :291-301