Zijian Tan , Shangyao Qin , Hong Liu , Xiao Huang, Yingyan Pu, Cheng He, Yimin Yuan, Zhida Su
{"title":"小分子将受损成人脊髓中的反应性星形胶质细胞重新编程为神经细胞","authors":"Zijian Tan , Shangyao Qin , Hong Liu , Xiao Huang, Yingyan Pu, Cheng He, Yimin Yuan, Zhida Su","doi":"10.1016/j.jare.2023.06.013","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><p>Ectopic expression of transcription factor-mediated <em>in vivo</em> neuronal reprogramming provides promising strategy to compensate for neuronal loss, while its further clinical application may be hindered by delivery and safety concerns. As a novel and attractive alternative, small molecules may offer a non-viral and non-integrative chemical approach for reprogramming cell fates. Recent definitive evidences have shown that small molecules can convert non-neuronal cells into neurons <em>in vitro</em>. However, whether small molecules alone can induce neuronal reprogramming <em>in vivo</em> remains largely unknown.</p></div><div><h3>Objectives</h3><p>To identify chemical compounds that can induce <em>in vivo</em> neuronal reprogramming in the adult spinal cord.</p></div><div><h3>Methods</h3><p>Immunocytochemistry, immunohistochemistry, qRT-PCR and fate-mapping are performed to analyze the role of small molecules in reprogramming astrocytes into neuronal cells <em>in vitro</em> and <em>in vivo</em>.</p></div><div><h3>Results</h3><p>By screening, we identify a chemical cocktail with only two chemical compounds that can directly and rapidly reprogram cultured astrocytes into neuronal cells. Importantly, this chemical cocktail can also successfully trigger neuronal reprogramming in the injured adult spinal cord without introducing exogenous genetic factors. These chemically induced cells showed typical neuronal morphologies and neuron-specific marker expression and could become mature and survive for more than 12 months. Lineage tracing indicated that the chemical compound-converted neuronal cells mainly originated from post-injury spinal reactive astrocytes.</p></div><div><h3>Conclusion</h3><p>Our proof-of-principle study demonstrates that <em>in vivo</em> glia-to-neuron conversion can be manipulated in a chemical compound-based manner. Albeit our current chemical cocktail has a low<!--> <!-->reprogramming efficiency, it will bring <em>in vivo</em> cell fate reprogramming closer to clinical application in brain and spinal cord repair. Future studies should focus on further refining our chemical cocktail and reprogramming approach to boost the reprogramming efficiency.</p></div>","PeriodicalId":14952,"journal":{"name":"Journal of Advanced Research","volume":"59 ","pages":"Pages 111-127"},"PeriodicalIF":11.4000,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2090123223001765/pdfft?md5=f5bd92d2971078e63bc108daeff21cd7&pid=1-s2.0-S2090123223001765-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Small molecules reprogram reactive astrocytes into neuronal cells in the injured adult spinal cord\",\"authors\":\"Zijian Tan , Shangyao Qin , Hong Liu , Xiao Huang, Yingyan Pu, Cheng He, Yimin Yuan, Zhida Su\",\"doi\":\"10.1016/j.jare.2023.06.013\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Introduction</h3><p>Ectopic expression of transcription factor-mediated <em>in vivo</em> neuronal reprogramming provides promising strategy to compensate for neuronal loss, while its further clinical application may be hindered by delivery and safety concerns. As a novel and attractive alternative, small molecules may offer a non-viral and non-integrative chemical approach for reprogramming cell fates. Recent definitive evidences have shown that small molecules can convert non-neuronal cells into neurons <em>in vitro</em>. However, whether small molecules alone can induce neuronal reprogramming <em>in vivo</em> remains largely unknown.</p></div><div><h3>Objectives</h3><p>To identify chemical compounds that can induce <em>in vivo</em> neuronal reprogramming in the adult spinal cord.</p></div><div><h3>Methods</h3><p>Immunocytochemistry, immunohistochemistry, qRT-PCR and fate-mapping are performed to analyze the role of small molecules in reprogramming astrocytes into neuronal cells <em>in vitro</em> and <em>in vivo</em>.</p></div><div><h3>Results</h3><p>By screening, we identify a chemical cocktail with only two chemical compounds that can directly and rapidly reprogram cultured astrocytes into neuronal cells. Importantly, this chemical cocktail can also successfully trigger neuronal reprogramming in the injured adult spinal cord without introducing exogenous genetic factors. These chemically induced cells showed typical neuronal morphologies and neuron-specific marker expression and could become mature and survive for more than 12 months. Lineage tracing indicated that the chemical compound-converted neuronal cells mainly originated from post-injury spinal reactive astrocytes.</p></div><div><h3>Conclusion</h3><p>Our proof-of-principle study demonstrates that <em>in vivo</em> glia-to-neuron conversion can be manipulated in a chemical compound-based manner. Albeit our current chemical cocktail has a low<!--> <!-->reprogramming efficiency, it will bring <em>in vivo</em> cell fate reprogramming closer to clinical application in brain and spinal cord repair. 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Small molecules reprogram reactive astrocytes into neuronal cells in the injured adult spinal cord
Introduction
Ectopic expression of transcription factor-mediated in vivo neuronal reprogramming provides promising strategy to compensate for neuronal loss, while its further clinical application may be hindered by delivery and safety concerns. As a novel and attractive alternative, small molecules may offer a non-viral and non-integrative chemical approach for reprogramming cell fates. Recent definitive evidences have shown that small molecules can convert non-neuronal cells into neurons in vitro. However, whether small molecules alone can induce neuronal reprogramming in vivo remains largely unknown.
Objectives
To identify chemical compounds that can induce in vivo neuronal reprogramming in the adult spinal cord.
Methods
Immunocytochemistry, immunohistochemistry, qRT-PCR and fate-mapping are performed to analyze the role of small molecules in reprogramming astrocytes into neuronal cells in vitro and in vivo.
Results
By screening, we identify a chemical cocktail with only two chemical compounds that can directly and rapidly reprogram cultured astrocytes into neuronal cells. Importantly, this chemical cocktail can also successfully trigger neuronal reprogramming in the injured adult spinal cord without introducing exogenous genetic factors. These chemically induced cells showed typical neuronal morphologies and neuron-specific marker expression and could become mature and survive for more than 12 months. Lineage tracing indicated that the chemical compound-converted neuronal cells mainly originated from post-injury spinal reactive astrocytes.
Conclusion
Our proof-of-principle study demonstrates that in vivo glia-to-neuron conversion can be manipulated in a chemical compound-based manner. Albeit our current chemical cocktail has a low reprogramming efficiency, it will bring in vivo cell fate reprogramming closer to clinical application in brain and spinal cord repair. Future studies should focus on further refining our chemical cocktail and reprogramming approach to boost the reprogramming efficiency.
期刊介绍:
Journal of Advanced Research (J. Adv. Res.) is an applied/natural sciences, peer-reviewed journal that focuses on interdisciplinary research. The journal aims to contribute to applied research and knowledge worldwide through the publication of original and high-quality research articles in the fields of Medicine, Pharmaceutical Sciences, Dentistry, Physical Therapy, Veterinary Medicine, and Basic and Biological Sciences.
The following abstracting and indexing services cover the Journal of Advanced Research: PubMed/Medline, Essential Science Indicators, Web of Science, Scopus, PubMed Central, PubMed, Science Citation Index Expanded, Directory of Open Access Journals (DOAJ), and INSPEC.