Reduced hippocampal neurogenesis in R6/2 transgenic Huntington's disease mice

被引:132
作者
Gil, JMAC
Mohapel, P
Araújo, IM
Popovic, N
Li, JY
Brundin, P
Petersén, Å
机构
[1] Lund Univ, Dept Expt Med Sci, Wallenberg Neurosci Ctr, Neuronal Survival Unit, SE-22184 Lund, Sweden
[2] Univ Coimbra, Fac Med, Ctr Neurosci & Cell Biol, P-3004504 Coimbra, Portugal
[3] Univ Coimbra, Fac Med, Inst Biochem, P-3004504 Coimbra, Portugal
[4] Univ Coimbra, Ctr Neurosci & Cell Biol, P-300451 Coimbra, Portugal
[5] Univ Coimbra, Dept Zool, P-300451 Coimbra, Portugal
关键词
BrdU; cell proliferation; dentate gyrus; doublecortin; Huntington's disease; Ki-67; neurogenesis; R6/2; mice; PCNA; subventricular zone;
D O I
10.1016/j.nbd.2005.05.006
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We investigated whether cell proliferation and neurogenesis are altered in R6/2 transgenic Huntington's disease mice. Using bromodeoxyuridine (BrdU), we found a progressive decrease in the number of proliferating cells in the dentate gyros of R6/2 mice. This reduction was detected in pre-symptomatic mice, and by 11.5 weeks, R6/2 mice had 66% fewer newly born cells in the hippocampus. The results were confirmed by immunohistochemistry for the cell cycle markers Ki-67 and proliferating cell nuclear antigen (PCNA). We did not observe changes in cell proliferation in the R6/2 subventricular zone, indicating that the decrease in cell proliferation is specific for the hippocampus. This decrease corresponded to a reduction in actual hippocampal neurogenesis as assessed by double immunostaining for BrdU and the neuronal marker neuronal nuclei (NeuN) and by immunohistochemistry for the neuroblast marker doublecortin. Reduced hippocampal neurogenesis may be a novel neuropathological feature in R6/2 mice that could be assessed when evaluating potential therapies. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:744 / 751
页数:8
相关论文
共 59 条
[1]   Neurodegeneration: a failure of neuroregeneration? [J].
Armstrong, RJE ;
Barker, RA .
LANCET, 2001, 358 (9288) :1174-1176
[2]   Neuronal replacement from endogenous precursors in the adult brain after stroke [J].
Arvidsson, A ;
Collin, T ;
Kirik, D ;
Kokaia, Z ;
Lindvall, O .
NATURE MEDICINE, 2002, 8 (09) :963-970
[3]   Adenoviral brain-derived neurotrophic factor induces both neostriatal and olfactory neuronal recruitment from endogenous progenitor cells in the adult forebrain [J].
Benraiss, A ;
Chmielnicki, E ;
Lerner, K ;
Roh, D ;
Goldman, SA .
JOURNAL OF NEUROSCIENCE, 2001, 21 (17) :6718-6731
[4]   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
[5]   Production of new cells in the rat dentate gyrus over the lifespan: relation to cognitive decline [J].
Bizon, JL ;
Gallagher, M .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2003, 18 (01) :215-219
[6]   The R6/2 transgenic mouse model of Huntington's disease develops diabetes due to deficient β-cell mass and exocytosis [J].
Björkqvist, M ;
Fex, M ;
Renström, E ;
Wierup, N ;
Petersén, Å ;
Gil, J ;
Bacos, K ;
Popovic, N ;
Li, JY ;
Sundler, F ;
Brundin, P ;
Mulder, H .
HUMAN MOLECULAR GENETICS, 2005, 14 (05) :565-574
[7]   Transient expression of doublecortin during adult neurogenesis [J].
Brown, JP ;
Couillard-Després, S ;
Cooper-Kuhn, CM ;
Winkler, J ;
Aigner, L ;
Kuhn, HG .
JOURNAL OF COMPARATIVE NEUROLOGY, 2003, 467 (01) :1-10
[8]   Brain-derived neurotrophic factor regulates the onset and severity of motor dysfunction associated with enkephalinergic neuronal degeneration in Huntington's disease [J].
Canals, JM ;
Pineda, JR ;
Torres-Peraza, JF ;
Bosch, M ;
Martín-Ibañez, R ;
Muñoz, MT ;
Mengod, G ;
Ernfors, P ;
Alberch, J .
JOURNAL OF NEUROSCIENCE, 2004, 24 (35) :7727-7739
[9]  
Carter RJ, 1999, J NEUROSCI, V19, P3248
[10]   Altered brain neurotransmitter receptors in transgenic mice expressing a portion of an abnormal human Huntington disease gene [J].
Cha, JHJ ;
Kosinski, CM ;
Kerner, JA ;
Alsdorf, SA ;
Mangiarini, L ;
Davies, SW ;
Penney, JB ;
Bates, GP ;
Young, AB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (11) :6480-6485