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Cell Surface Antigen Display for Neuronal Differentiation-Specific Tracking

Cell therapeutic agents for treating degenerative brain diseases using neural stem cells are actively being developed. However, few systems have been developed to monitor in real time whether the transplanted neural stem cells are actually differentiated into neurons. Therefore, it is necessary to d...

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Detalles Bibliográficos
Autores principales: Kim, Sang Chul, Lee, Eun-Hye, Yu, Ji Hea, Kim, Sang-Mi, Nam, Bae-Geun, Chung, Hee Yong, Kim, Yeon-Soo, Cho, Sung-Rae, Park, Chang-Hwan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Applied Pharmacology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6319552/
https://www.ncbi.nlm.nih.gov/pubmed/30458601
http://dx.doi.org/10.4062/biomolther.2018.110
Descripción
Sumario:Cell therapeutic agents for treating degenerative brain diseases using neural stem cells are actively being developed. However, few systems have been developed to monitor in real time whether the transplanted neural stem cells are actually differentiated into neurons. Therefore, it is necessary to develop a technology capable of specifically monitoring neuronal differentiation in vivo. In this study, we established a system that expresses cell membrane-targeting red fluorescent protein under control of the Synapsin promoter in order to specifically monitor differentiation from neural stem cells into neurons. In order to overcome the weak expression level of the tissue-specific promoter system, the partial 5′ UTR sequence of Creb was added for efficient expression of the cell surface-specific antigen. This system was able to track functional neuronal differentiation of neural stem cells transplanted in vivo, which will help improve stem cell therapies.