Cargando…
Multiphoton imaging of neural structure and activity in Drosophila through the intact cuticle
We developed a multiphoton imaging method to capture neural structure and activity in behaving flies through the intact cuticle. Our measurements showed that the fly head cuticle has surprisingly high transmission at wavelengths >900nm, and the difficulty of through-cuticle imaging is due to the...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8846588/ https://www.ncbi.nlm.nih.gov/pubmed/35073257 http://dx.doi.org/10.7554/eLife.69094 |
_version_ | 1784651874546221056 |
---|---|
author | Aragon, Max Jameson Mok, Aaron T Shea, Jamien Wang, Mengran Kim, Haein Barkdull, Nathan Xu, Chris Yapici, Nilay |
author_facet | Aragon, Max Jameson Mok, Aaron T Shea, Jamien Wang, Mengran Kim, Haein Barkdull, Nathan Xu, Chris Yapici, Nilay |
author_sort | Aragon, Max Jameson |
collection | PubMed |
description | We developed a multiphoton imaging method to capture neural structure and activity in behaving flies through the intact cuticle. Our measurements showed that the fly head cuticle has surprisingly high transmission at wavelengths >900nm, and the difficulty of through-cuticle imaging is due to the air sacs and/or fat tissue underneath the head cuticle. By compressing or removing the air sacs, we performed multiphoton imaging of the fly brain through the intact cuticle. Our anatomical and functional imaging results show that 2- and 3-photon imaging are comparable in superficial regions such as the mushroom body, but 3-photon imaging is superior in deeper regions such as the central complex and beyond. We further demonstrated 2-photon through-cuticle functional imaging of odor-evoked calcium responses from the mushroom body γ-lobes in behaving flies short term and long term. The through-cuticle imaging method developed here extends the time limits of in vivo imaging in flies and opens new ways to capture neural structure and activity from the fly brain. |
format | Online Article Text |
id | pubmed-8846588 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-88465882022-02-16 Multiphoton imaging of neural structure and activity in Drosophila through the intact cuticle Aragon, Max Jameson Mok, Aaron T Shea, Jamien Wang, Mengran Kim, Haein Barkdull, Nathan Xu, Chris Yapici, Nilay eLife Neuroscience We developed a multiphoton imaging method to capture neural structure and activity in behaving flies through the intact cuticle. Our measurements showed that the fly head cuticle has surprisingly high transmission at wavelengths >900nm, and the difficulty of through-cuticle imaging is due to the air sacs and/or fat tissue underneath the head cuticle. By compressing or removing the air sacs, we performed multiphoton imaging of the fly brain through the intact cuticle. Our anatomical and functional imaging results show that 2- and 3-photon imaging are comparable in superficial regions such as the mushroom body, but 3-photon imaging is superior in deeper regions such as the central complex and beyond. We further demonstrated 2-photon through-cuticle functional imaging of odor-evoked calcium responses from the mushroom body γ-lobes in behaving flies short term and long term. The through-cuticle imaging method developed here extends the time limits of in vivo imaging in flies and opens new ways to capture neural structure and activity from the fly brain. eLife Sciences Publications, Ltd 2022-01-24 /pmc/articles/PMC8846588/ /pubmed/35073257 http://dx.doi.org/10.7554/eLife.69094 Text en © 2022, Aragon et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Aragon, Max Jameson Mok, Aaron T Shea, Jamien Wang, Mengran Kim, Haein Barkdull, Nathan Xu, Chris Yapici, Nilay Multiphoton imaging of neural structure and activity in Drosophila through the intact cuticle |
title | Multiphoton imaging of neural structure and activity in Drosophila through the intact cuticle |
title_full | Multiphoton imaging of neural structure and activity in Drosophila through the intact cuticle |
title_fullStr | Multiphoton imaging of neural structure and activity in Drosophila through the intact cuticle |
title_full_unstemmed | Multiphoton imaging of neural structure and activity in Drosophila through the intact cuticle |
title_short | Multiphoton imaging of neural structure and activity in Drosophila through the intact cuticle |
title_sort | multiphoton imaging of neural structure and activity in drosophila through the intact cuticle |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8846588/ https://www.ncbi.nlm.nih.gov/pubmed/35073257 http://dx.doi.org/10.7554/eLife.69094 |
work_keys_str_mv | AT aragonmaxjameson multiphotonimagingofneuralstructureandactivityindrosophilathroughtheintactcuticle AT mokaaront multiphotonimagingofneuralstructureandactivityindrosophilathroughtheintactcuticle AT sheajamien multiphotonimagingofneuralstructureandactivityindrosophilathroughtheintactcuticle AT wangmengran multiphotonimagingofneuralstructureandactivityindrosophilathroughtheintactcuticle AT kimhaein multiphotonimagingofneuralstructureandactivityindrosophilathroughtheintactcuticle AT barkdullnathan multiphotonimagingofneuralstructureandactivityindrosophilathroughtheintactcuticle AT xuchris multiphotonimagingofneuralstructureandactivityindrosophilathroughtheintactcuticle AT yapicinilay multiphotonimagingofneuralstructureandactivityindrosophilathroughtheintactcuticle |