Kannan Geetha, Crawford Joshua A, Yang ChunXia, Gressitt Kristin L, Ihenatu Chinezimuzo, Krasnova Irina N, Cadet Jean Lud, Yolken Robert H, Severance Emily G, Pletnikov Mikhail V
Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, 600 North Wolfe Street, Baltimore, MD 21287, USA.
Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, 600 North Wolfe Street, Baltimore, MD 21287, USA.
Neurobiol Dis. 2016 Jul;91:307-14. doi: 10.1016/j.nbd.2016.03.005. Epub 2016 Mar 8.
Toxoplasma gondii is a pathogen implicated in psychiatric disorders. As elevated antibodies to T. gondii are also present in non-symptomatic individuals, we hypothesized that the age during first exposure to the pathogen may affect symptom manifestation. We tested this hypothesis by evaluating neurobehavioral abnormalities and the immune response in mice following adolescent or adult T. gondii infection.
Mice were infected with T. gondii at postnatal day 33 (adolescent/juvenile) or 61 (adult). At 8weeks post-infection (wpi), pre-pulse inhibition of the acoustic startle (PPI) in mice administered MK-801 (0.1 and 0.3mg/kg) and amphetamine (5 and 10mg/kg) was assessed. Peripheral (anti-T. gondii, C1q-associated IgG and anti-GLUN2 antibodies) and central (C1q and Iba1) markers of the immune response were also evaluated. In addition, regional brain expression of N-methyl-d-aspartate receptor (NMDAR) subunits (GLUN1 and GLUN2A), glutamatergic (vGLUT1, PSD95) and GABAergic (GAD67) markers, and monoamines (DA, NE, 5-HT) and their metabolites were measured.
Juvenile and adult infected mice exhibited opposite effects of MK-801 on PPI, with decreased PPI in juveniles and increased PPI in adults. There was a significantly greater elevation of GLUN2 autoantibodies in juvenile-compared to adult-infected mice. In addition, age-dependent differences were found in regional expression of NMDAR subunits and markers of glutamatergic, GABAergic, and monoaminergic systems. Activated microglia and C1q elevations were found in both juvenile- and adult-T. gondii infected mice.
Our study demonstrates that the age at first exposure to T. gondii is an important factor in shaping distinct behavioral and neurobiological abnormalities. Elevation in GLUN2 autoantibodies or complement protein C1q may be a potential underlying mechanism. A better understanding of these age-related differences may lead to more efficient treatments of behavioral disorders associated with T. gondii infection.
弓形虫是一种与精神疾病有关的病原体。由于无症状个体中也存在弓形虫抗体升高的情况,我们推测首次接触该病原体的年龄可能会影响症状表现。我们通过评估青春期或成年期感染弓形虫后小鼠的神经行为异常和免疫反应来验证这一假设。
在出生后第33天(青春期/幼年)或61天(成年期)给小鼠感染弓形虫。在感染后8周(wpi),评估给予MK-801(0.1和0.3mg/kg)和苯丙胺(5和10mg/kg)的小鼠的听觉惊吓前脉冲抑制(PPI)。还评估了免疫反应的外周标志物(抗弓形虫、C1q相关IgG和抗GLUN2抗体)和中枢标志物(C1q和Iba1)。此外,测量了N-甲基-D-天冬氨酸受体(NMDAR)亚基(GLUN1和GLUN2A)、谷氨酸能标志物(vGLUT1、PSD95)和γ-氨基丁酸能标志物(GAD67)的区域脑表达,以及单胺(多巴胺、去甲肾上腺素、5-羟色胺)及其代谢产物。
幼年和成年感染小鼠对MK-801的PPI反应相反,幼年小鼠的PPI降低,成年小鼠的PPI升高。与成年感染小鼠相比,幼年感染小鼠中GLUN2自身抗体的升高明显更大。此外,在NMDAR亚基以及谷氨酸能、γ-氨基丁酸能和单胺能系统标志物的区域表达中发现了年龄依赖性差异。在幼年和成年感染弓形虫的小鼠中均发现了活化的小胶质细胞和C1q升高。
我们的研究表明,首次接触弓形虫的年龄是形成不同行为和神经生物学异常的重要因素。GLUN2自身抗体或补体蛋白C1q的升高可能是潜在的机制。更好地理解这些与年龄相关的差异可能会导致更有效地治疗与弓形虫感染相关的行为障碍。