Texas Tech University Health Sciences Center El Paso, Department of Molecular and Translational Medicine, Center of Emphasis in Neurosciences, Graduate School of Biomedical Sciences, Paul L Foster School of Medicine, 5001 El Paso Dr, El Paso, TX 79905, United States of America.
Texas Tech University Health Sciences Center El Paso, Department of Molecular and Translational Medicine, Center of Emphasis in Neurosciences, Graduate School of Biomedical Sciences, Paul L Foster School of Medicine, 5001 El Paso Dr, El Paso, TX 79905, United States of America.
Exp Neurol. 2020 Mar;325:113120. doi: 10.1016/j.expneurol.2019.113120. Epub 2019 Nov 18.
Multiple system atrophy (MSA) is a fatal disorder with no effective treatment. MSA pathology is characterized by α-synuclein (aSyn) accumulation in oligodendrocytes, the myelinating glial cells of the central nervous system (CNS). aSyn accumulation in oligodendrocytes forms the pathognomonic glial cytoplasmic inclusions (GCIs) of MSA. MSA aSyn pathology is also associated with motor and autonomic dysfunction, including an impaired ability to sweat. MSA patients have abnormal CNS expression of glial-cell-line-derived neurotrophic factor (GDNF) and brain-derived neurotrophic factor (BDNF). Our prior studies using the parent compound FTY720, a food and drug administration (FDA) approved immunosuppressive for multiple sclerosis, reveal that FTY720 protects parkinsonian mice by increasing BDNF. Our FTY720-derivative, FTY720-Mitoxy, is known to increase expression of oligodendrocyte BDNF, GDNF, and nerve growth factor (NGF) but does not reduce levels of circulating lymphocytes as it is not phosphorylated so cannot modulate sphingosine 1 phosphate receptors (S1PRs). To preclinically assess FTY720-Mitoxy for MSA, we used mice expressing human aSyn in oligodendrocytes under a 2,' 3'-cyclic nucleotide 3'-phosphodiesterase (CNP) promoter. CNP-aSyn transgenic (Tg) mice develop motor dysfunction between 7 and 9 mo, and progressive GCI pathology. Using liquid chromatography-mass spectrometry (LC-MS/MS) and enzymatic assays, we confirmed that FTY720-Mitoxy was stable and active. Vehicle or FTY720-Mitoxy (1.1 mg/kg/day) was delivered to wild type (WT) or Tg littermates from 8.5-11.5 mo by osmotic pump. We behaviorally assessed their movement by rotarod and sweat production by starch‑iodine test. Postmortem tissues were evaluated by qPCR for BDNF, GDNF, NGF and GDNF-receptor RET mRNA and for aSyn, BDNF, GDNF, and Iba1 protein by immunoblot. MicroRNAs (miRNAs) were also assessed by qPCR. FTY720-Mitoxy normalized movement, sweat function and soleus muscle mass in 11.5 mo Tg MSA mice. FTY720-Mitoxy also increased levels of brain GDNF and reduced brain miR-96-5p, a miRNA that acts to decrease GDNF expression. Moreover, FTY720-Mitoxy blocked aSyn pathology measured by sequential protein extraction and immunoblot, and microglial activation assessed by immunohistochemistry and immunoblot. In the 3-nitropropionic acid (3NP) toxin model of MSA, FTY720-Mitoxy protected movement and mitochondria in WT and CNP-aSyn Tg littermates. Our data confirm potent in vivo protection by FTY720-Mitoxy, supporting its further evaluation as a potential therapy for MSA and related synucleinopathies.
多系统萎缩症(MSA)是一种致命的疾病,目前尚无有效的治疗方法。MSA 病理学的特征是中枢神经系统(CNS)中的少突胶质细胞中α-突触核蛋白(aSyn)的积累。少突胶质细胞中的 aSyn 积累形成 MSA 的特征性神经胶质细胞质包涵体(GCIs)。MSA 的 aSyn 病理学也与运动和自主功能障碍有关,包括出汗能力受损。MSA 患者的 CNS 中存在胶质细胞源性神经营养因子(GDNF)和脑源性神经营养因子(BDNF)的异常表达。我们之前使用母体化合物 FTY720 的研究表明,FTY720 是一种获得美国食品和药物管理局(FDA)批准的多发性硬化症的免疫抑制剂,它通过增加 BDNF 来保护帕金森病小鼠。我们的 FTY720 衍生物 FTY720-Mitoxy 已知可增加少突胶质细胞 BDNF、GDNF 和神经生长因子(NGF)的表达,但不会降低循环淋巴细胞的水平,因为它不会被磷酸化,因此不能调节鞘氨醇 1 磷酸受体(S1PRs)。为了在临床上评估 FTY720-Mitoxy 对 MSA 的作用,我们使用了在 2'、3'-环核苷酸 3'-磷酸二酯酶(CNP)启动子下在少突胶质细胞中表达人 aSyn 的小鼠。CNP-aSyn 转基因(Tg)小鼠在 7 至 9 月龄之间出现运动功能障碍,并逐渐出现 GCI 病理学。使用液相色谱-质谱联用(LC-MS/MS)和酶联测定法,我们证实 FTY720-Mitoxy 稳定且具有活性。从 8.5 至 11.5 月龄开始,通过渗透泵向野生型(WT)或 Tg 同窝仔鼠输送载体或 FTY720-Mitoxy(1.1mg/kg/天)。我们通过旋转棒评估它们的运动能力,通过淀粉-碘试验评估它们的出汗能力。通过 qPCR 评估死后组织中的 BDNF、GDNF、NGF 和 GDNF 受体 RET mRNA,通过免疫印迹评估 aSyn、BDNF、GDNF 和 Iba1 蛋白。还通过 qPCR 评估 microRNAs(miRNAs)。FTY720-Mitoxy 使 11.5 月龄 Tg MSA 小鼠的运动、汗液功能和比目鱼肌质量正常化。FTY720-Mitoxy 还增加了大脑 GDNF 的水平,并降低了大脑 miR-96-5p 的水平,miR-96-5p 是一种降低 GDNF 表达的 miRNA。此外,FTY720-Mitoxy 通过连续蛋白质提取和免疫印迹测量阻断了 aSyn 病理学,并通过免疫组织化学和免疫印迹测量阻断了小胶质细胞激活。在 MSA 的 3-硝基丙酸(3NP)毒素模型中,FTY720-Mitoxy 保护 WT 和 CNP-aSyn Tg 同窝仔鼠的运动和线粒体。我们的数据证实了 FTY720-Mitoxy 具有强大的体内保护作用,支持进一步将其评估为 MSA 和相关突触核蛋白病的潜在治疗方法。