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老化雄性和雌性 Fischer 344 大鼠社会相关脑区小胶质细胞的体视学分析。

Stereological Analysis of Microglia in Aged Male and Female Fischer 344 Rats in Socially Relevant Brain Regions.

机构信息

Behavioral Neuroscience Program, Department of Psychology, Binghamton University-SUNY, Binghamton, NY 13902-6000, United States.

Behavioral Neuroscience Program, Department of Psychology, Binghamton University-SUNY, Binghamton, NY 13902-6000, United States.

出版信息

Neuroscience. 2018 May 1;377:40-52. doi: 10.1016/j.neuroscience.2018.02.028. Epub 2018 Feb 26.

Abstract

Aging is associated with a substantial decline in the expression of social behavior as well as increased neuroinflammation. Since immune activation and subsequent increased expression of cytokines can suppress social behavior in young rodents, we examined age and sex differences in microglia within brain regions critical to social behavior regulation (PVN, BNST, and MEA) as well as in the hippocampus. Adult (3-month) and aged (18-month) male and female F344 (N = 26, n = 5-8/group) rats were perfused and Iba-1 immunopositive microglia were assessed using unbiased stereology and optical density. For stereology, microglia were classified based on the following criteria: (1) thin ramified processes, (2) thick long processes, (3) stout processes, or (4) round/ameboid shape. Among the structures examined, the highest density of microglia was evident in the BNST and MEA. Aged rats of both sexes displayed increased total number of microglia number exclusively in the MEA. Sex differences also emerged, whereby aged females (but not males) displayed greater total number of microglia in the BNST relative to their young adult counterparts. When morphological features of microglia were assessed, aged rats exhibited increased soma size in the BNST, MEA, and CA3. Together, these findings provide a comprehensive characterization of microglia number and morphology under ambient conditions in CNS sites critical for the normal expression of social processes. To the extent that microglia morphology is predictive of reactivity and subsequent cytokine release, these data suggest that the expression of social behavior in late aging may be adversely influenced by heightened inflammation.

摘要

衰老是与社会行为表达的显著下降以及神经炎症的增加相关的。由于免疫激活和随后细胞因子表达的增加可以抑制年轻啮齿动物的社会行为,我们研究了对社会行为调节(PVN、BNST 和 MEA)以及海马体至关重要的大脑区域中与年龄和性别相关的小胶质细胞差异。成年(3 个月)和老年(18 个月)雄性和雌性 F344(N=26,n=5-8/组)大鼠进行灌注,使用无偏立体学和光密度评估 Iba-1 免疫阳性小胶质细胞。对于立体学,小胶质细胞根据以下标准进行分类:(1)薄分支突起,(2)厚长突起,(3)粗壮突起,或(4)圆形/阿米巴样形状。在所检查的结构中,BNST 和 MEA 中可见最高密度的小胶质细胞。两性老年大鼠仅在 MEA 中表现出小胶质细胞总数的增加。性别差异也出现了,即老年雌性(而非雄性)与年轻成年雌性相比,BNST 中的小胶质细胞总数更多。当评估小胶质细胞的形态特征时,老年大鼠在 BNST、MEA 和 CA3 中的体大小增大。总之,这些发现为中枢神经系统中对社会过程正常表达至关重要的关键部位的小胶质细胞数量和形态提供了全面的特征描述。在小胶质细胞形态可预测反应性和随后细胞因子释放的程度上,这些数据表明,晚期衰老中社会行为的表达可能会受到炎症加剧的不利影响。

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