Department of Neurosurgery, Emory University School of Medicine, Atlanta, GA, United States.
Department of Neurosurgery, Emory University School of Medicine, Atlanta, GA, United States; Interdisciplinary Bioengineering Graduate Program, Georgia Institute of Technology, Atlanta, GA, United States; School of Chemical and Biomolecular Engineering, Georgia Institute of Technology, Atlanta, GA, United States.
Neuroscience. 2020 Aug 21;442:183-192. doi: 10.1016/j.neuroscience.2020.07.006. Epub 2020 Jul 9.
The bacterial exoenzyme C3 transferase (C3) irreversibly inhibits RhoA GTPase leading to stimulation of axonal outgrowth in injured neurons. C3 has been used successfully in models of neurotrauma and shows promise as an option to support cell survival and axonal growth of dopaminergic (DA) neurons in Parkinson's disease (PD) cell therapy. Whether the continuous expression of C3 in DA neurons is well-tolerated is unknown. To assess the potential neurotoxicity of sustained expression of C3 in DA neurons, we generated Cre recombinase-dependent adeno-associated viral vectors (AAV) for targeted C3 delivery to DA neurons of the mouse substantia nigra pars compacta (SNc). The effect of continuous expression of C3 on DA neurons was assessed by immunohistochemistry and compared to that of Enhanced Yellow Fluorescent Protein (EYFP) as negative controls. We did not find significant reduction of tyrosine hydroxylase (TH) expression levels nor the presence of cleaved activated caspase 3. Astrocytic activation as determined by GFAP expression was comparable to EYFP controls. To evaluate the impact of C3 expression on striatal terminals of the nigrostriatal pathway, we compared the rotational behavior of wildtype mice injected unilaterally with either C3 or 6-hydroxydopamine (6-OHDA). Mice injected with C3 exhibited similar ipsiversive rotations to the site of injection in comparison to control mice injected with EYFP and significantly fewer ipsiversive rotations compared to 6-OHDA lesioned mice. Non-significant difference between C3 and EYFP controls in behavioral and histological analyses demonstrate that transduced DA neurons express C3 continuously without apparent adverse effects, supporting the use of C3 in efficacy studies targeting DA neurons.
细菌外切酶 C3 转移酶 (C3) 不可逆地抑制 RhoA GTP 酶,导致损伤神经元中的轴突生长刺激。C3 已成功应用于神经创伤模型,并有望成为支持帕金森病 (PD) 细胞治疗中多巴胺能 (DA) 神经元存活和轴突生长的选择。持续表达 C3 在 DA 神经元中是否耐受良好尚不清楚。为了评估持续表达 C3 在 DA 神经元中的潜在神经毒性,我们生成了 Cre 重组酶依赖性腺相关病毒载体 (AAV),用于将 C3 靶向递送到小鼠黑质致密部 (SNc) 的 DA 神经元。通过免疫组织化学评估持续表达 C3 对 DA 神经元的影响,并与增强型黄色荧光蛋白 (EYFP) 作为阴性对照进行比较。我们没有发现酪氨酸羟化酶 (TH) 表达水平的显著降低,也没有发现激活的半胱天冬酶 3 的存在。胶质细胞激活程度通过 GFAP 表达与 EYFP 对照相当。为了评估 C3 表达对黑质纹状体通路纹状体末端的影响,我们比较了单侧注射 C3 或 6-羟多巴胺 (6-OHDA) 的野生型小鼠的旋转行为。与注射 EYFP 的对照小鼠相比,注射 C3 的小鼠在注射部位表现出相似的向侧旋转,与 6-OHDA 损伤的小鼠相比,向侧旋转明显减少。C3 和 EYFP 对照在行为和组织学分析中的非显著性差异表明,转导的 DA 神经元持续表达 C3 而没有明显的不良反应,支持 C3 在针对 DA 神经元的疗效研究中的使用。