Kim Hyun-Jin, Fan Xiaotang, Gabbi Chiara, Yakimchuk Konstantin, Parini Paolo, Warner Margaret, Gustafsson Jan-Ake
Department of Biosciences and Nutrition, Karolinska Institutet, Novum, SE-14186 Stockholm, Sweden.
Proc Natl Acad Sci U S A. 2008 Feb 12;105(6):2094-9. doi: 10.1073/pnas.0711599105. Epub 2008 Jan 31.
Administration of beta-sitosterol (42 mg/kg per day) for 3 weeks to 8-month-old male LXRbeta-/- mice resulted in the death of motor neurons in the lumbar region of the spinal cord and loss of tyrosine hydroxylase-positive dopaminergic neurons in the substantia nigra. In mice at 5 months of age, beta-sitosterol had no observed toxicity but at 16 months of age, it caused severe paralysis and symptoms typical of dopaminergic dysfunction in LXRbeta-/- mice. WT mice were not affected by these doses of beta-sitosterol. In 5-month-old mice, levels of the intestinal transporters, ABCG5/8 and Niemann-Pick C1 Like 1, were not affected by loss of liver X receptor (LXR) beta and/or treatment with beta-sitosterol nor were there changes in plasma levels of cholesterol or beta-sitosterol. In 8-month-old LXRbeta-/- mice there was activation of microglia in the substantia nigra pars reticulata and aggregates of ubiquitin and TDP-43 in the cytoplasm of large motor neurons in the lumbar spinal cord. Brain cholesterol concentrations were higher in LXRbeta-/- than in their WT counterparts, and treatment with beta-sitosterol reduced brain cholesterol in both WT and LXRbeta-/- mice. In LXRbeta-/- mice but not in WT mice levels of 24-hydrocholesterol were increased upon beta-sitosterol treatment. These data indicate that multiple mechanisms are involved in the sensitivity of LXRbeta-/- mice to beta-sitosterol. These include activation of microglia, accumulation of protein aggregates in the cytoplasm of large motor neurons, and depletion of brain cholesterol.
给8月龄雄性肝脏X受体β(LXRβ)基因敲除小鼠每天服用β-谷甾醇(42毫克/千克),持续3周,结果导致脊髓腰段运动神经元死亡,黑质中酪氨酸羟化酶阳性多巴胺能神经元丧失。在5月龄小鼠中,β-谷甾醇未观察到毒性,但在16月龄小鼠中,它导致LXRβ基因敲除小鼠出现严重麻痹和典型的多巴胺能功能障碍症状。野生型(WT)小鼠不受这些剂量β-谷甾醇的影响。在5月龄小鼠中,肠道转运蛋白ABCG5/8和尼曼-匹克C1样蛋白1的水平不受肝脏X受体(LXR)β缺失和/或β-谷甾醇处理的影响,血浆胆固醇或β-谷甾醇水平也没有变化。在8月龄LXRβ基因敲除小鼠中,黑质网状部小胶质细胞活化,腰髓大型运动神经元细胞质中出现泛素和TDP-43聚集物。LXRβ基因敲除小鼠的脑胆固醇浓度高于野生型同窝小鼠,β-谷甾醇处理可降低野生型和LXRβ基因敲除小鼠的脑胆固醇。在LXRβ基因敲除小鼠中,β-谷甾醇处理后24-羟胆固醇水平升高,而野生型小鼠则未出现这种情况。这些数据表明,多种机制参与了LXRβ基因敲除小鼠对β-谷甾醇的敏感性。这些机制包括小胶质细胞活化、大型运动神经元细胞质中蛋白质聚集体的积累以及脑胆固醇的消耗。