Transverse sinus injections drive robust whole-brain expression of transgenes
Convenient, efficient and fast whole-brain delivery of transgenes presents a persistent experimental challenge in neuroscience. Recent advances demonstrate whole-brain gene delivery by retro-orbital injection of virus, but slow and sparse expression and the large injection volumes required make this...
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doaj-d45d828452294e4ea5d747710a78cf482021-05-05T21:06:38ZengeLife Sciences Publications LtdeLife2050-084X2020-05-01910.7554/eLife.53639Transverse sinus injections drive robust whole-brain expression of transgenesAli S Hamodi0https://orcid.org/0000-0002-8398-170XAude Martinez Sabino1N Dalton Fitzgerald2https://orcid.org/0000-0001-7794-6898Dionysia Moschou3Michael C Crair4Department of Neuroscience, Yale School of Medicine, New Haven, United StatesDepartment of Neuroscience, Yale School of Medicine, New Haven, United States; University of Technology of Compiègne, Compiègne, FranceDepartment of Neuroscience, Yale School of Medicine, New Haven, United StatesDepartment of Neuroscience, Yale School of Medicine, New Haven, United StatesDepartment of Neuroscience, Yale School of Medicine, New Haven, United States; Department of Ophthalmology and Visual Science, Yale School of Medicine, New Haven, United States; Kavli Institute for Neuroscience, Yale School of Medicine, New Haven, United StatesConvenient, efficient and fast whole-brain delivery of transgenes presents a persistent experimental challenge in neuroscience. Recent advances demonstrate whole-brain gene delivery by retro-orbital injection of virus, but slow and sparse expression and the large injection volumes required make this approach cumbersome, especially for developmental studies. We developed a novel method for efficient gene delivery across the central nervous system in neonatal mice and rats starting as early as P1 and persisting into adulthood. The method employs transverse sinus injections of 2–4 μL of AAV9 at P0. Here, we describe how to use this method to label and/or genetically manipulate cells in the neonatal rat and mouse brain. The protocol is fast, simple, can be readily adopted by any laboratory, and utilizes the widely available AAV9 capsid. The procedure is adaptable for diverse experimental applications ranging from biochemistry, anatomical and functional mapping, gene expression, silencing, and editing.https://elifesciences.org/articles/53639transverse sinus injectionwhole-brain expressionneonatemouseratviral vector |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ali S Hamodi Aude Martinez Sabino N Dalton Fitzgerald Dionysia Moschou Michael C Crair |
spellingShingle |
Ali S Hamodi Aude Martinez Sabino N Dalton Fitzgerald Dionysia Moschou Michael C Crair Transverse sinus injections drive robust whole-brain expression of transgenes eLife transverse sinus injection whole-brain expression neonate mouse rat viral vector |
author_facet |
Ali S Hamodi Aude Martinez Sabino N Dalton Fitzgerald Dionysia Moschou Michael C Crair |
author_sort |
Ali S Hamodi |
title |
Transverse sinus injections drive robust whole-brain expression of transgenes |
title_short |
Transverse sinus injections drive robust whole-brain expression of transgenes |
title_full |
Transverse sinus injections drive robust whole-brain expression of transgenes |
title_fullStr |
Transverse sinus injections drive robust whole-brain expression of transgenes |
title_full_unstemmed |
Transverse sinus injections drive robust whole-brain expression of transgenes |
title_sort |
transverse sinus injections drive robust whole-brain expression of transgenes |
publisher |
eLife Sciences Publications Ltd |
series |
eLife |
issn |
2050-084X |
publishDate |
2020-05-01 |
description |
Convenient, efficient and fast whole-brain delivery of transgenes presents a persistent experimental challenge in neuroscience. Recent advances demonstrate whole-brain gene delivery by retro-orbital injection of virus, but slow and sparse expression and the large injection volumes required make this approach cumbersome, especially for developmental studies. We developed a novel method for efficient gene delivery across the central nervous system in neonatal mice and rats starting as early as P1 and persisting into adulthood. The method employs transverse sinus injections of 2–4 μL of AAV9 at P0. Here, we describe how to use this method to label and/or genetically manipulate cells in the neonatal rat and mouse brain. The protocol is fast, simple, can be readily adopted by any laboratory, and utilizes the widely available AAV9 capsid. The procedure is adaptable for diverse experimental applications ranging from biochemistry, anatomical and functional mapping, gene expression, silencing, and editing. |
topic |
transverse sinus injection whole-brain expression neonate mouse rat viral vector |
url |
https://elifesciences.org/articles/53639 |
work_keys_str_mv |
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