
Neurod1 and Ascl1 Convert Human Astrocytes into Neurons in Ex Vivo Culture of Human Brain Tissue
简介:
- 作者: Liang Xu, Qing-Song Wang, Jian-Cheng Liao, Jia-Jun Zheng, Bing Qin, Wen Li, Jia-Xuan Zhang, Wei Li, Xiang-Yu Wang, Mao-Ying Zhang, Gong Chen
- 杂志: Neurology eJournal
- Doi: https://www.doi.org/10.2139/ssrn.4378268
- 出版日期: 2023 Mar 21
论文中使用的产品/服务
Quotation shows PackGene:Adeno-associated virus (AAV): AAV9 GFAP::Cre, AAV9 CAG::Flex-GFP and AAV9 CAG::Flex-NeuroD1-GFP were produced by PackGene Biotech.
Research Field:CNS
AAV Serotype:AAV9
Targeted organ:human brain slices
摘要
Transcription factor-mediated cell conversion has been reported in the central nervous system (CNS) of both rodents and non-human primates (NHPs). In particular, astrocyte-to-neuron (AtN) conversion has been achieved in the brain and spinal cord of animal models of neurological disorders for neural regeneration and repair. However, whether AtN conversion can be ultimately used for human brain repair in patients is still unknown. To investigate the applicability of AtN conversion technology in human brain, we established a long-term ex vivo culture system using human brain tissue that is surgically removed from epileptic patients to directly test AtN conversion in human astrocytes. We demonstrate that both neural transcription factors NeuroD1 and Ascl1 can convert human astrocytes into neurons. Importantly, both immunostaining and electrophysiological recordings revealed that the astrocyte-converted neurons showed immature properties during initial 1-2 weeks of conversion, and then acquired more mature properties after 3-4 weeks of conversion. These studies in ex vivo human brain tissue pave a stepping stone toward future clinical trials using transcription factor-based AtN conversion approach to treat neurological disorders.
关于派真
作为一家专注于AAV 技术十余年,深耕基因治疗领域的CRO&CDMO,派真生物可提供从载体设计、构建到 AAV、慢病毒和 mRNA 服务的一站式解决方案。凭借深厚的技术实力、卓越的运营管理和高标准的服务交付,我们为全球客户提供一站式CMC解决方案,包括从早期概念验证、成药性评估到IIT、IND及BLA的各个阶段。
凭借我们独立知识产权的π-alphaTM 293 细胞AAV高产技术平台,我们能将AAV产量提高多至10倍,每批次产量可达1×10¹⁷vg,以满足多样化的商业化和临床项目需求。此外,我们定制化的mRNA和脂质纳米颗粒(LNP)产品及服务覆盖药物和疫苗开发的各个阶段,从研发到符合GMP的生产,提供端到端的一站式解决方案。
