Chronic stress-induced disruption of the astrocyte network is driven by structural atrophy and not loss of astrocytes

被引:157
作者
Tynan, Ross J. [1 ,2 ,4 ]
Beynon, Sarah B. [1 ,2 ,4 ]
Hinwood, Madeleine [1 ,2 ,4 ]
Johnson, Sarah J. [3 ]
Nilsson, Michael [2 ,4 ]
Woods, Jason J. [1 ,2 ,4 ]
Walker, Frederick R. [1 ,2 ,4 ]
机构
[1] Univ Newcastle, Sch Biomed Sci & Pharm, Newcastle, NSW 2308, Australia
[2] Univ Newcastle, Ctr Brain & Mental Hlth Res, Newcastle, NSW 2308, Australia
[3] Univ Newcastle, Sch Elect Engn & Comp Sci, Newcastle, NSW 2308, Australia
[4] Hunter Med Res Inst, Newcastle, NSW, Australia
基金
英国医学研究理事会;
关键词
Astrocyte; Chronic stress; GFAP; S100; beta; Infralimbic prefrontal cortex; SUBGENUAL PREFRONTAL CORTEX; FIBRILLARY ACIDIC PROTEIN; GLIAL PATHOLOGY; RAT MODEL; BRAIN; MICROGLIA; HIPPOCAMPUS; MORPHOLOGY; ABNORMALITIES; DISEASE;
D O I
10.1007/s00401-013-1102-0
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Chronic stress is well recognized to decrease the number of GFAP(+) astrocytes within the prefrontal cortex (PFC). Recent research, however, has suggested that our understanding of how stress alters astrocytes may be incomplete. Specifically, chronic stress has been shown to induce a unique form of microglial remodelling, but it is not yet clear whether astrocytes also undergo similar structural modifications. Such alterations may be significant given the role of astrocytes in modulating synaptic function. Accordingly, in the current study we have examined changes in astrocyte morphology following exposure to chronic stress in adult rats, using three-dimensional digital reconstructions of astrocytes. Our analysis indicated that chronic stress produced profound atrophy of astrocyte process length, branching and volume. We additionally examined changes in astrocyte-specific S100 beta, which are both a putative astrocyte marker and a protein whose expression is associated with astrocyte distress. While we found that S100 beta levels were increased by stress, this increase was not correlated with atrophy. We further established that while chronic stress was associated with a decrease in astrocyte numbers when GFAP labelling was used as a marker, we could find no evidence of a decrease in the total number of cells, based on Nissl staining, or in the number of S100 beta(+) cells. This finding suggests that chronic stress may not actually reduce astrocyte numbers and may instead selectively decrease GFAP expression. The results of the current study are significant as they indicate stress-induced astrocyte-mediated disturbances may not be due to a loss of cells but rather due to significant remodeling of the astrocyte network.
引用
收藏
页码:75 / 91
页数:17
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