Role of cell cycle proteins in CNS injury

被引:120
作者
Byrnes, Kimberly R. [1 ]
Faden, Alan I. [1 ]
机构
[1] Georgetown Univ, Med Ctr, Dept Neurosci, Washington, DC 20057 USA
关键词
brain injury; flavopiridol; proliferation; review; spinal cord injury; stroke;
D O I
10.1007/s11064-007-9312-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Following trauma or ischemia to the central nervous system (CNS), there is a marked increase in the expression of cell cycle-related proteins. This up-regulation is associated with apoptosis of post-mitotic cells, including neurons and oligodendrocytes, both in vitro and in vivo. Cell cycle activation also induces proliferation of astrocytes and microglia, contributing to the glial scar and microglial activation with release of inflammatory factors. Treatment with cell cycle inhibitors in CNS injury models inhibits glial scar formation and neuronal cell death, resulting in substantially decreased lesion volumes and improved behavioral recovery. Here we critically review the role of cell cycle pathways in the pathophysiology of experimental stroke, traumatic brain injury and spinal cord injury, and discuss the potential of cell cycle inhibitors as neuroprotective agents.
引用
收藏
页码:1799 / 1807
页数:9
相关论文
共 79 条
[31]
Microglial cell cycle-associated proteins control microglial proliferation in vivo and in vitro and are regulated by GM-CSF and density-dependent inhibition [J].
Koguchi, K ;
Nakatsuji, Y ;
Okuno, T ;
Sawada, M ;
Sakoda, S .
JOURNAL OF NEUROSCIENCE RESEARCH, 2003, 74 (06) :898-905
[32]
Cyclin D1 is an essential mediator of apoptotic neuronal cell death [J].
Kranenburg, O ;
vanderEb, A ;
Zantema, A .
EMBO JOURNAL, 1996, 15 (01) :46-54
[33]
Cell cycle activation linked to neuronal cell death initiated by DNA damage [J].
Kruman, II ;
Wersto, RP ;
Cardozo-Pelaez, F ;
Smilenov, L ;
Chan, SL ;
Chrest, FJ ;
Emokpae, R ;
Gorospe, M ;
Mattson, MP .
NEURON, 2004, 41 (04) :549-561
[34]
Hypoxia-ischemia induces DNA synthesis without cell proliferation in dying neurons in adult rodent brain [J].
Kuan, CY ;
Schloemer, AJ ;
Lu, AG ;
Burns, KA ;
Weng, WL ;
Williams, MT ;
Strauss, KI ;
Vorhees, CV ;
Flavell, RA ;
Davis, RJ ;
Sharp, FR ;
Rakic, P .
JOURNAL OF NEUROSCIENCE, 2004, 24 (47) :10763-10772
[35]
The brain-specific activator p35 allows Cdk5 to escape inhibition by p27(Kip1) in neurons [J].
Lee, MH ;
Nikolic, M ;
Baptista, CA ;
Lai, E ;
Tsai, LH ;
Massague, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (08) :3259-3263
[36]
TEMPORAL REGULATION OF CYCLIN A-P107 AND P33(CDK2) COMPLEXES BINDING TO A HUMAN THYMIDINE KINASE PROMOTER ELEMENT IMPORTANT FOR G1-S PHASE TRANSCRIPTIONAL REGULATION [J].
LI, LJ ;
NAEVE, GS ;
LEE, AS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (08) :3554-3558
[37]
B-myb and C-myb play required roles in neuronal apoptosis evoked by nerve growth factor deprivation and DNA damage [J].
Liu, DX ;
Biswas, SC ;
Greene, LA .
JOURNAL OF NEUROSCIENCE, 2004, 24 (40) :8720-8725
[38]
Regulation of neuronal survival and death by E2F-dependent gene repression and derepression [J].
Liu, DX ;
Greene, LA .
NEURON, 2001, 32 (03) :425-438
[39]
Apoptosis and brain ischaemia [J].
Love, S .
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2003, 27 (02) :267-282
[40]
McGraw J, 2001, J NEUROSCI RES, V63, P109, DOI 10.1002/1097-4547(20010115)63:2<109::AID-JNR1002>3.0.CO