Nomaru Hiroko, Sakumi Kunihiko, Katogi Atsuhisa, Ohnishi Yoshinori N, Kajitani Kosuke, Tsuchimoto Daisuke, Nestler Eric J, Nakabeppu Yusaku
Division of Neurofunctional Genomics, Department of Immunobiology and Neuroscience, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
Glia. 2014 Aug;62(8):1284-98. doi: 10.1002/glia.22680. Epub 2014 Apr 25.
The Fosb gene encodes subunits of the activator protein-1 transcription factor complex. Two mature mRNAs, Fosb and ΔFosb, encoding full-length FOSB and ΔFOSB proteins respectively, are formed by alternative splicing of Fosb mRNA. Fosb products are expressed in several brain regions. Moreover, Fosb-null mice exhibit depressive-like behaviors and adult-onset spontaneous epilepsy, demonstrating important roles in neurological and psychiatric disorders. Study of Fosb products has focused almost exclusively on neurons; their function in glial cells remains to be explored. In this study, we found that microglia express equivalent levels of Fosb and ΔFosb mRNAs to hippocampal neurons and, using microarray analysis, we identified six microglial genes whose expression is dependent on Fosb products. Of these genes, we focused on C5ar1 and C5ar2, which encode receptors for complement C5a. In isolated Fosb-null microglia, chemotactic responsiveness toward the truncated form of C5a was significantly lower than that in wild-type cells. Fosb-null mice were significantly resistant to kainate-induced seizures compared with wild-type mice. C5ar1 mRNA levels and C5aR1 immunoreactivity were increased in wild-type hippocampus 24 hours after kainate administration; however, such induction was significantly reduced in Fosb-null hippocampus. Furthermore, microglial activation after kainate administration was significantly diminished in Fosb-null hippocampus, as shown by significant reductions in CD68 immunoreactivity, morphological change and reduced levels of Il6 and Tnf mRNAs, although no change in the number of Iba-1-positive cells was observed. These findings demonstrate that, under excitotoxicity, Fosb products contribute to a neuroinflammatory response in the hippocampus through regulation of microglial C5ar1 and C5ar2 expression.
Fosb基因编码激活蛋白-1转录因子复合物的亚基。通过Fosb mRNA的可变剪接形成两种成熟的mRNA,即Fosb和ΔFosb,它们分别编码全长FOSB和ΔFOSB蛋白。Fosb产物在多个脑区表达。此外,Fosb基因敲除小鼠表现出抑郁样行为和成年期自发性癫痫,表明其在神经和精神疾病中起重要作用。对Fosb产物的研究几乎完全集中在神经元上;它们在胶质细胞中的功能仍有待探索。在本研究中,我们发现小胶质细胞表达的Fosb和ΔFosb mRNA水平与海马神经元相当,并且通过微阵列分析,我们鉴定出六个小胶质细胞基因,其表达依赖于Fosb产物。在这些基因中,我们重点研究了C5ar1和C5ar2,它们编码补体C5a的受体。在分离的Fosb基因敲除小胶质细胞中,对截短形式的C5a的趋化反应性明显低于野生型细胞。与野生型小鼠相比,Fosb基因敲除小鼠对海藻酸诱导的癫痫发作具有显著抗性。在给予海藻酸24小时后,野生型海马中C5ar1 mRNA水平和C5aR1免疫反应性增加;然而,在Fosb基因敲除海马中这种诱导明显减少。此外,Fosb基因敲除海马中海藻酸给药后小胶质细胞的激活明显减弱,表现为CD68免疫反应性显著降低、形态变化以及Il6和Tnf mRNA水平降低,尽管未观察到Iba-1阳性细胞数量的变化。这些发现表明,在兴奋性毒性作用下,Fosb产物通过调节小胶质细胞C5ar1和C5ar2的表达,促进海马中的神经炎症反应。