Age-changes in gene expression in primary mixed glia cultures from young vs. old rat cerebral cortex are modified by interactions with neurons

被引:5
作者
Kremsky, Isaac
Morgan, Todd E.
Hou, Xiaogang
Li, Lei
Finch, Caleb E. [1 ]
机构
[1] Univ So Calif, Dept Biol Sci, Los Angeles, CA 90089 USA
关键词
GFAP; Mixed glia; Aging; Affymetrix microarray; Glial-neuron interactions; FIBRILLARY ACIDIC PROTEIN; AGING BRAIN; IN-VITRO; ALZHEIMERS-DISEASE; NEURITE OUTGROWTH; ASTROCYTES; ACTIVATION; HIPPOCAMPAL; GROWTH; VIVO;
D O I
10.1016/j.bbi.2011.12.008
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Astrocytic GFAP expression increases during normal aging in many brain regions and in primary astrocyte cultures derived from aging rodent brains. As shown below, we unexpectedly found that the age-related increase of GFAP expression was suppressed in mixed glia (astrocytes + microglia). However, the age-related increase of GFAP was observed when E18 neurons were co-cultured with mixed glia. Thus, the presence of microglia can suppress the age-related increase of GFAP, in primary cultures of astrocytes. To more broadly characterize how aging and co-culture with neurons alters glial gene expression, we profiled gene expression in mixed glia from young (3 mo) and old (24 mo) male rat cerebral cortex by Affymetrix microarray (Rat230 2.0). The majority of age changes were independent of the presence of neurons. Overall, the expression of twofold more genes increased with age than decreased with age. The minority of age changes that were either suppressed or revealed by the presence of neurons may be useful to analyze glial-neuron interaction during aging. Some in vitro changes are shared with those of aging rat hippocampus in studies from the Landfield group (Rowe et al., 2007; Kadish et al., 2009). (c) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:797 / 802
页数:6
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