Kongsui R, Johnson S J, Graham B A, Nilsson M, Walker F R
School of Biomedical Sciences and Pharmacy, University of Newcastle, Callaghan, NSW, Australia; Centre for Translational Neuroscience and Mental Health Research, University of Newcastle, Callaghan, NSW, Australia; Hunter Medical Research Institute, University of Newcastle, Callaghan, NSW, Australia.
School of Electrical Engineering and Computer Science, University of Newcastle, Callaghan, NSW, Australia; Hunter Medical Research Institute, University of Newcastle, Callaghan, NSW, Australia.
Neuroscience. 2015 Dec 3;310:629-40. doi: 10.1016/j.neuroscience.2015.09.061. Epub 2015 Oct 9.
Sickness behaviors have become the focus of great interest in recent years as they represent a clear case of how peripheral disturbances in immune signaling can disrupt quite complex behaviors. In the current study, we were interested in examining whether we could identify any significant morphological disturbances in microglia associated with these sickness-like behaviors in adult male Sprague-Dawley rats. We chose lipopolysaccharide (LPS 100 μg/kg/i.p.), to induce sickness-like behaviors as it is the most well-validated approach to do so in rodents and humans. We were particularly interested in examining changes in microglia within the prefrontal cortex (PFC) as several recent neuroimaging studies have highlighted significant functional changes in this region following peripheral LPS administration. Paraformaldehyde-fixed tissue was collected from animals 24h post LPS administration and labeled immunohistochemically with an antibody directed to bind to Iba-1, a protein known to be involved in the structural remodeling of microglia. To analyze changes, we have made use of two recently described image analysis procedures. The first is known as cumulative threshold spectra (CTS) analysis. The second involves the unsupervised digital reconstruction of microglia. We undertook these complementary analysis of microglial cells in the both the pre- and infralimbic divisions of the PFC. Our results indicated that microglial soma size was significantly enlarged, while cell processes had contracted slightly following LPS administration. To our knowledge this study is to first to definitely demonstrate substantial microglial disturbances within the PFC following LPS delivered at a dose that was sufficient to induce significant sickness-like behavior.
疾病行为近年来已成为人们极大关注的焦点,因为它们清楚地表明了免疫信号传导中的外周干扰是如何扰乱相当复杂的行为的。在当前的研究中,我们感兴趣的是,在成年雄性斯普拉格-道利大鼠中,能否识别出与这些疾病样行为相关的小胶质细胞的任何显著形态学干扰。我们选择脂多糖(LPS 100 μg/kg/i.p.)来诱导疾病样行为,因为这是在啮齿动物和人类中最经过充分验证的方法。我们特别感兴趣的是检查前额叶皮层(PFC)内小胶质细胞的变化,因为最近的几项神经影像学研究强调了外周给予LPS后该区域的显著功能变化。在给予LPS 24小时后从动物身上收集多聚甲醛固定的组织,并用一种针对Iba-1的抗体进行免疫组织化学标记,Iba-1是一种已知参与小胶质细胞结构重塑的蛋白质。为了分析变化,我们使用了最近描述的两种图像分析程序。第一种称为累积阈值光谱(CTS)分析。第二种涉及小胶质细胞的无监督数字重建。我们对PFC的前边缘和下边缘分区中的小胶质细胞进行了这些补充分析。我们的结果表明,给予LPS后,小胶质细胞的胞体大小显著增大,而细胞突起略有收缩。据我们所知,这项研究首次明确证明了在给予足以诱导显著疾病样行为的剂量的LPS后,PFC内存在实质性的小胶质细胞干扰。