Chen Zhilong, Fan Guoqing, Li Anan, Yuan Jing, Xu Tonghui
Britton Chance Center for Biomedical Photonics, Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, Wuhan, China.
MoE Key Laboratory for Biomedical Photonics, Collaborative Innovation Center for Biomedical Engineering, School of Engineering Sciences, Huazhong University of Science and Technology, Wuhan, China.
Mol Ther Methods Clin Dev. 2019 Nov 21;17:21-33. doi: 10.1016/j.omtm.2019.11.006. eCollection 2020 Jun 12.
The motor system controls muscle movement through lower motor neurons in the spinal cord and brainstem. Lower motor neurons are efferent neurons in the central nervous system (CNS) characterized by axonal projections that reach specific targets in the periphery. Lower motor neuron lesions result in the denervation and dysfunction of peripheral skeletal muscle. Great progress has been made to develop therapeutic strategies to transduce lower motor neurons with genes. However, the widespread distribution of lower motor neurons makes their specific, extensive, and efficient transduction a challenge. In this study, we demonstrated that, compared to the other tested recombinant adeno-associated virus (rAAV) serotypes, rAAV2-retro mediated the most efficient retrograde transduction of lower motor neurons in the spinal cord following intramuscular injection in neonatal mice. A single injection of rAAV2-retro in a single muscle enabled the efficient and extensive transduction of lower motor neurons in the spinal cord and brainstem rather than transducing only the lower motor neurons connected to the injected muscle. rAAV2-retro achieved the extensive transduction of lower motor neurons by the cerebrospinal fluid pathway. Our work suggests that gene delivery via the intramuscular injection of rAAV2-retro represents a promising tool in the development of gene therapy strategies for motor neuron diseases.
运动系统通过脊髓和脑干中的下运动神经元控制肌肉运动。下运动神经元是中枢神经系统(CNS)中的传出神经元,其特征是轴突投射到达外周的特定靶点。下运动神经元损伤会导致外周骨骼肌去神经支配和功能障碍。在开发用基因转导下运动神经元的治疗策略方面已经取得了很大进展。然而,下运动神经元的广泛分布使得它们的特异性、广泛和高效转导成为一项挑战。在本研究中,我们证明,与其他测试的重组腺相关病毒(rAAV)血清型相比,rAAV2-retro在新生小鼠肌肉注射后介导脊髓中下运动神经元最有效的逆行转导。在一块肌肉中单次注射rAAV2-retro能够有效且广泛地转导脊髓和脑干中的下运动神经元,而不是仅转导与注射肌肉相连的下运动神经元。rAAV2-retro通过脑脊液途径实现了下运动神经元的广泛转导。我们的工作表明,通过肌肉注射rAAV2-retro进行基因递送是运动神经元疾病基因治疗策略开发中有前景的工具。