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Targeting microglia with lentivirus and AAV: Recent advances and remaining challenges

Microglia have emerged as a critical component of neurodegenerative diseases. Genetic manipulation of microglia can elucidate their functional impact in disease. In neuroscience, recombinant viruses such as lentiviruses and adeno-associated viruses (AAVs) have been successfully used to target variou...

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Detalles Bibliográficos
Autores principales: Maes, Margaret E., Colombo, Gloria, Schulz, Rouven, Siegert, Sandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Scientific Publishers Ireland 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6734419/
https://www.ncbi.nlm.nih.gov/pubmed/31158432
http://dx.doi.org/10.1016/j.neulet.2019.134310
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author Maes, Margaret E.
Colombo, Gloria
Schulz, Rouven
Siegert, Sandra
author_facet Maes, Margaret E.
Colombo, Gloria
Schulz, Rouven
Siegert, Sandra
author_sort Maes, Margaret E.
collection PubMed
description Microglia have emerged as a critical component of neurodegenerative diseases. Genetic manipulation of microglia can elucidate their functional impact in disease. In neuroscience, recombinant viruses such as lentiviruses and adeno-associated viruses (AAVs) have been successfully used to target various cell types in the brain, although effective transduction of microglia is rare. In this review, we provide a short background of lentiviruses and AAVs, and strategies for designing recombinant viral vectors. Then, we will summarize recent literature on successful microglial transductions in vitro and in vivo, and discuss the current challenges. Finally, we provide guidelines for reporting the efficiency and specificity of viral targeting in microglia, which will enable the microglial research community to assess and improve methodologies for future studies.
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spelling pubmed-67344192019-09-14 Targeting microglia with lentivirus and AAV: Recent advances and remaining challenges Maes, Margaret E. Colombo, Gloria Schulz, Rouven Siegert, Sandra Neurosci Lett Article Microglia have emerged as a critical component of neurodegenerative diseases. Genetic manipulation of microglia can elucidate their functional impact in disease. In neuroscience, recombinant viruses such as lentiviruses and adeno-associated viruses (AAVs) have been successfully used to target various cell types in the brain, although effective transduction of microglia is rare. In this review, we provide a short background of lentiviruses and AAVs, and strategies for designing recombinant viral vectors. Then, we will summarize recent literature on successful microglial transductions in vitro and in vivo, and discuss the current challenges. Finally, we provide guidelines for reporting the efficiency and specificity of viral targeting in microglia, which will enable the microglial research community to assess and improve methodologies for future studies. Elsevier Scientific Publishers Ireland 2019-08-10 /pmc/articles/PMC6734419/ /pubmed/31158432 http://dx.doi.org/10.1016/j.neulet.2019.134310 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Maes, Margaret E.
Colombo, Gloria
Schulz, Rouven
Siegert, Sandra
Targeting microglia with lentivirus and AAV: Recent advances and remaining challenges
title Targeting microglia with lentivirus and AAV: Recent advances and remaining challenges
title_full Targeting microglia with lentivirus and AAV: Recent advances and remaining challenges
title_fullStr Targeting microglia with lentivirus and AAV: Recent advances and remaining challenges
title_full_unstemmed Targeting microglia with lentivirus and AAV: Recent advances and remaining challenges
title_short Targeting microglia with lentivirus and AAV: Recent advances and remaining challenges
title_sort targeting microglia with lentivirus and aav: recent advances and remaining challenges
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6734419/
https://www.ncbi.nlm.nih.gov/pubmed/31158432
http://dx.doi.org/10.1016/j.neulet.2019.134310
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