Age-related changes of astorocytes, oligodendrocytes and microglia in the mouse hippocampal CA1 sector

被引:90
作者
Hayakawa, Natsumi
Kato, Hiroyuki
Araki, Tsutomu
机构
[1] Univ Tokushima, Grad Sch, Dept Neurobiol & Therapeut, Tokushima 7708505, Japan
[2] Univ Tokushima, Fac Pharmaceut Sci, Tokushima 7708505, Japan
[3] Int Univ Hlth & Welf, Dept Neurol, Organized Ctr Clin Med, Tochigi, Japan
关键词
ageing; hippocampal CA1 sector; immunohistochemistry; astrocyte; oligodendrocyte; microglia; mice; FIBRILLARY ACIDIC PROTEIN; DEPENDENT ALTERATIONS; MPTP NEUROTOXICITY; GENE-EXPRESSION; DENTATE GYRUS; NITRIC-OXIDE; CELL-DEATH; MEMORY; ASTROCYTES; INCREASES;
D O I
10.1016/j.mad.2007.01.005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We investigated the age-related alterations of astorocyte, oligodendrocyte and rnicroglia in the mouse hippocampal CA I sector under the same conditions using immunohistochemistry. Glial fibrillary acidic protein (GFAP), 2', 3-cyclic nucleotide 3'-phosphodiesterase (CNPase) and isolectin 134 immunoreactivity was measured in 2-, 8-, 18-, 40-42- and 50-59-week -old mice. Total number of GFAP-positive cells was unchanged in the hippocampal CAI sector up to 40-42 weeks of birth. In 50-59-week-old mice, however, a significant increase in the number of GFAP-positive cells was observed in the hippocampal CA] sector, exhibiting the morphology of reactive astrocytes. In contrast, the fibers of CNPase immunoreactivity were unchanged in the hippocampal CA] sector up to 18 weeks of birth. In 40-42- and 50-59-week-old mice, however, a significant decrease in the densities of CNPase-positive fibers was observed in the hippocampal CAI sector. On the other hand, total number of isolectin B4-positive cells was unchanged in the hippocampal CA] sector up to 40-42 weeks of birth. In 50-59-week-old mice, however, a significant decrease in the number of isolectin B4-POSitive cells was observed in the hippocampal CAI sector. Our results show that astrocytes proliferate and are activated in the hippocampal CAI sector with advancing age. Furthermore, the present study demonstrates that the fibers of oligodendrocytes and total number of microglial cells in the hippocampal CAI sector are decreased during ageing processes. These results suggest that age-related changes of astorocytes, oligodendrocytes and microglia had Occurred in the mouse hippocampal CAI sector. (C) 2007 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:311 / 316
页数:6
相关论文
共 51 条
[1]   MEMORY DEFICITS ASSOCIATED WITH SENESCENCE - NEUROPHYSIOLOGICAL AND BEHAVIORAL-STUDY IN THE RAT [J].
BARNES, CA .
JOURNAL OF COMPARATIVE AND PHYSIOLOGICAL PSYCHOLOGY, 1979, 93 (01) :74-104
[2]   AGING AND THE PHYSIOLOGY OF SPATIAL MEMORY [J].
BARNES, CA .
NEUROBIOLOGY OF AGING, 1988, 9 (5-6) :563-568
[3]  
BJORKLUND H, 1985, EXP BRAIN RES, V58, P163
[4]   Hippocampal neuron and synaptophysin-positive bouton number in aging C57BL/6 mice [J].
Calhoun, ME ;
Kurth, D ;
Phinney, AL ;
Long, JM ;
Hengemihle, J ;
Mouton, PR ;
Ingram, DK ;
Jucker, M .
NEUROBIOLOGY OF AGING, 1998, 19 (06) :599-606
[5]   Glial reaction in the hippocampal formation is highly correlated with aging in human brain [J].
David, JP ;
Ghozali, F ;
FalletBianco, C ;
Wattez, A ;
Delaine, S ;
Boniface, B ;
DiMenza, C ;
Delacourte, A .
NEUROSCIENCE LETTERS, 1997, 235 (1-2) :53-56
[6]   AGE-DEPENDENT ALTERATIONS IN HIPPOCAMPAL SYNAPTIC PLASTICITY - RELATION TO MEMORY DISORDERS [J].
DETOLEDOMORRELL, L ;
GEINISMAN, Y ;
MORRELL, F .
NEUROBIOLOGY OF AGING, 1988, 9 (5-6) :581-590
[7]   The hippocampus and declarative memory: cognitive mechanisms and neural codes [J].
Eichenbaum, H .
BEHAVIOURAL BRAIN RESEARCH, 2001, 127 (1-2) :199-207
[8]   Increased chemokine gene expression during aging in the murine brain [J].
Felzien, LK ;
McDonald, JT ;
Gleason, SM ;
Berman, NEJ ;
Klein, RM .
BRAIN RESEARCH, 2001, 890 (01) :137-146
[9]  
Finch C E, 2002, Adv Gerontol, V10, P35
[10]   ANIMAL-MODELS OF NORMAL AGING - RELATIONSHIP BETWEEN COGNITIVE DECLINE AND MARKERS IN HIPPOCAMPAL CIRCUITRY [J].
GALLAGHER, M ;
NICOLLE, MM .
BEHAVIOURAL BRAIN RESEARCH, 1993, 57 (02) :155-162