Mechanisms underlying neural cell death in neurodegenerative diseases: alterations of a developmentally-mediated cellular rheostat

被引:49
作者
Mehler, MF
Gokhan, S
机构
[1] Yeshiva Univ Albert Einstein Coll Med, Einstein Comprehens Canc Ctr, Rose F Kennedy Ctr Res Mental Retardat & Dev Disa, Dept Neurol, Bronx, NY 10461 USA
[2] Yeshiva Univ Albert Einstein Coll Med, Einstein Comprehens Canc Ctr, Rose F Kennedy Ctr Res Mental Retardat & Dev Disa, Dept Neurosci & Psychiat, Bronx, NY 10461 USA
关键词
D O I
10.1016/S0166-2236(00)01705-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Genes associated with neurodegenerative diseases are normally expressed throughout neural development and are essential for the elaboration and maintenance of neuronal subpopulations, Disease-causing mutations can compromise defined subsets of these neural specification events in subtle ways that initially lead to impairments in the cellular homeostasis of evolving regional neuronal subpopulations, and adult-onset cell death from normally non-lethal environmental stressors, Neurodegenerative diseases may, therefore, represent an emerging class of developmental disorders characterized by novel biological responses to subthreshold neurodevelopmental abnormalities that impair targeted neuronal biosynthetic pathways without causing obvious developmental deficits. This developmental model of pathogenesis predicts that it will soon be possible to identify these dysfunctional pathways prior to the occurrence of irreversible cellular injury, and to successfully intervene using innovative neuroprotective and neural regenerative strategies.
引用
收藏
页码:599 / 605
页数:9
相关论文
共 69 条
[1]   Presenilin 1 protein directly interacts with Bcl-2 [J].
Alberici, A ;
Moratto, D ;
Benussi, L ;
Gasparini, L ;
Ghidoni, R ;
Gatta, LB ;
Finazzi, D ;
Frison, GB ;
Trabucchi, M ;
Growdon, JH ;
Nitsch, RM ;
Binetti, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (43) :30764-30769
[2]  
Arnold J, 1998, PROG BRAIN RES, V117, P23
[3]   Notch signaling: Cell fate control and signal integration in development [J].
Artavanis-Tsakonas, S ;
Rand, MD ;
Lake, RJ .
SCIENCE, 1999, 284 (5415) :770-776
[4]  
Bhide PG, 1996, J NEUROSCI, V16, P5523
[5]   Severe deficiencies in dopamine signaling in presymptomatic Huntington's disease mice [J].
Bibb, JA ;
Yan, Z ;
Svenningsson, P ;
Snyder, GL ;
Pieribone, VA ;
Horiuchi, A ;
Nairn, AC ;
Messer, A ;
Greengard, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (12) :6809-6814
[6]   Aberrant interactions of transcriptional repressor proteins with the Huntington's disease gene product, huntingtin [J].
Boutell, JM ;
Thomas, P ;
Neal, JW ;
Weston, VJ ;
Duce, J ;
Harper, PS ;
Jones, AL .
HUMAN MOLECULAR GENETICS, 1999, 8 (09) :1647-1655
[7]  
Buttini M, 1999, J NEUROSCI, V19, P4867
[8]  
Capell A, 1997, J NEUROCHEM, V69, P2432
[9]   A one-hit model of cell death in inherited neuronal degenerations [J].
Clarke, G ;
Collins, RA ;
Leavitt, BR ;
Andrews, DF ;
Hayden, MR ;
Lumsden, CJ ;
McInnes, RR .
NATURE, 2000, 406 (6792) :195-199
[10]   The synucleins: a family of proteins involved in synaptic function, plasticity, neurodegeneration and disease [J].
Clayton, DF ;
George, JM .
TRENDS IN NEUROSCIENCES, 1998, 21 (06) :249-254