Ayzenberg Ilya, Schlevogt Sibylle, Metzdorf Judith, Stahlke Sarah, Pedreitturia Xiomara, Hunfeld Anika, Couillard-Despres Sebastien, Kleiter Ingo
Department of Neurology, St. Josef-Hospital, Ruhr-University, Bochum, Germany.
Department of Animal Physiology, Ruhr-University, Bochum, Germany.
PLoS One. 2015 Mar 17;10(3):e0118550. doi: 10.1371/journal.pone.0118550. eCollection 2015.
Bioluminescence imaging is a sensitive approach for longitudinal neuroimaging. Transgenic mice expressing luciferase under the promoter of doublecortin (DCX-luc), a specific marker of neuronal progenitor cells (NPC), allow monitoring of neurogenesis in living mice. Since the extent and time course of neurogenesis during autoimmune brain inflammation are controversial, we investigated neurogenesis in MOG-peptide induced experimental allergic encephalomyelitis (EAE) using DCX-luc reporter mice. We observed a marked, 2- to 4-fold increase of the bioluminescence signal intensity 10 days after EAE induction and a gradual decline 1-2 weeks thereafter. In contrast, immunostaining for DCX revealed no differences between EAE and control mice 2 and 4 weeks after immunization in zones of adult murine neurogenesis such as the dentate gyrus. Ex vivo bioluminescence imaging showed similar luciferase expression in brain homogenates of EAE and control animals. Apart from complete immunization including MOG-peptide also incomplete immunization with complete Freund´s adjuvant and pertussis toxin resulted in a rapid increase of the in vivo bioluminescence signal. Blood-brain barrier (BBB) leakage was demonstrated 10 days after both complete and incomplete immunization and might explain the increased bioluminescence signal in vivo. We conclude, that acute autoimmune inflammation in EAE does not alter neurogenesis, at least at the stage of DCX-expressing NPC. Effects of immunization on the BBB integrity must be considered when luciferase is used as a reporter within the CNS during the active stage of EAE. Models with stable CNS-restricted luciferase expression could serve as technically convenient way to evaluate BBB integrity in a longitudinal manner.
生物发光成像技术是一种用于纵向神经成像的灵敏方法。在双皮质素(DCX-luc)启动子控制下表达荧光素酶的转基因小鼠,其中双皮质素是神经元祖细胞(NPC)的一种特异性标志物,可用于监测活体小鼠的神经发生情况。由于自身免疫性脑炎症期间神经发生的程度和时间进程存在争议,我们使用DCX-luc报告基因小鼠,研究了髓鞘少突胶质细胞糖蛋白(MOG)肽诱导的实验性自身免疫性脑脊髓炎(EAE)中的神经发生情况。我们观察到,在EAE诱导后10天,生物发光信号强度显著增加了2至4倍,此后1至2周逐渐下降。相比之下,在成年小鼠神经发生区域如齿状回,免疫组化显示在免疫后2周和4周,EAE小鼠与对照小鼠之间的双皮质素没有差异。离体生物发光成像显示,EAE小鼠和对照动物的脑匀浆中荧光素酶表达相似。除了使用MOG肽进行完全免疫外,使用完全弗氏佐剂和百日咳毒素进行不完全免疫也导致体内生物发光信号迅速增加。在完全免疫和不完全免疫后10天均证实存在血脑屏障(BBB)渗漏,这可能解释了体内生物发光信号增加的原因。我们得出结论,EAE中的急性自身免疫炎症至少在表达DCX的NPC阶段不会改变神经发生。在EAE活动期,当在中枢神经系统内使用荧光素酶作为报告基因时,必须考虑免疫对BBB完整性的影响。具有稳定的中枢神经系统限制性荧光素酶表达的模型可以作为一种技术上简便的方法,用于纵向评估BBB的完整性。