-
Je něco špatně v tomto záznamu ?
Advancing the path to in-vivo imaging in freely moving mice via multimode-multicore fiber based holographic endoscopy
Y. Du, E. Dylda, M. Stibůrek, AD. Gomes, S. Turtaev, JMP. Pakan, T. Čižmár
Status neindexováno Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články
NLK
Directory of Open Access Journals
od 2019
PubMed Central
od 2014
ProQuest Central
od 2019-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2014
- Publikační typ
- časopisecké články MeSH
SIGNIFICANCE: Hair-thin multimode optical fiber-based holographic endoscopes have gained considerable interest in modern neuroscience for their ability to achieve cellular and even subcellular resolution during in-vivo deep brain imaging. However, the application of multimode fibers in freely moving animals presents a persistent challenge as it is difficult to maintain optimal imaging performance while the fiber undergoes deformations. AIM: We propose a fiber solution for challenging in-vivo applications with the capability of deep brain high spatial resolution imaging and neuronal activity monitoring in anesthetized as well as awake behaving mice. APPROACH: We used our previously developed M3CF multimode-multicore fiber to record fluorescently labeled neurons in anesthetized mice. Our M3CF exhibits a cascaded refractive index structure, enabling two distinct regimes of light transport that imitate either a multimode or a multicore fiber. The M3CF has been specifically designed for use in the initial phase of an in-vivo experiment, allowing for the navigation of the endoscope's distal end toward the targeted brain structure. The multicore regime enables the transfer of light to and from each individual neuron within the field of view. For chronic experiments in awake behaving mice, it is crucial to allow for disconnecting the fiber and the animal between experiments. Therefore, we provide here an effective solution and establish a protocol for reconnection of two segments of M3CF with hexagonally arranged corelets. RESULTS: We successfully utilized the M3CF to image neurons in anaesthetized transgenic mice expressing enhanced green fluorescent protein. Additionally, we compared imaging results obtained with the M3CF with larger numerical aperture (NA) fibers in fixed whole-brain tissue. CONCLUSIONS: This study focuses on addressing challenges and providing insights into the use of multimode-multicore fibers as imaging solutions for in-vivo applications. We suggest that the upcoming version of the M3CF increases the overall NA between the two cladding layers to allow for access to high resolution spatial imaging. As the NA increases in the multimode regime, the fiber diameter and ring structure must be reduced to minimize the computational burden and invasiveness.
Center for Behavioral Brain Sciences Magdeburg Germany
Friedrich Schiller University Jena Institute of Applied Optics Jena Germany
German Centre for Neurodegenerative Diseases Magdeburg Germany
Institute of Scientific Instruments of CAS Brno Czechia
Leibniz Institute for Neurobiology Magdeburg Germany
Leibniz Institute of Photonic Technology Jena Germany
University of Chinese Academy of Sciences Hangzhou Institute for Advanced Study Hangzhou China
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc24005497
- 003
- CZ-PrNML
- 005
- 20240412130934.0
- 007
- ta
- 008
- 240405s2024 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1117/1.NPh.11.S1.S11506 $2 doi
- 035 __
- $a (PubMed)38352728
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Du, Yang $u University of Chinese Academy of Sciences, Hangzhou Institute for Advanced Study, Hangzhou, China $u Leibniz Institute of Photonic Technology, Jena, Germany
- 245 10
- $a Advancing the path to in-vivo imaging in freely moving mice via multimode-multicore fiber based holographic endoscopy / $c Y. Du, E. Dylda, M. Stibůrek, AD. Gomes, S. Turtaev, JMP. Pakan, T. Čižmár
- 520 9_
- $a SIGNIFICANCE: Hair-thin multimode optical fiber-based holographic endoscopes have gained considerable interest in modern neuroscience for their ability to achieve cellular and even subcellular resolution during in-vivo deep brain imaging. However, the application of multimode fibers in freely moving animals presents a persistent challenge as it is difficult to maintain optimal imaging performance while the fiber undergoes deformations. AIM: We propose a fiber solution for challenging in-vivo applications with the capability of deep brain high spatial resolution imaging and neuronal activity monitoring in anesthetized as well as awake behaving mice. APPROACH: We used our previously developed M3CF multimode-multicore fiber to record fluorescently labeled neurons in anesthetized mice. Our M3CF exhibits a cascaded refractive index structure, enabling two distinct regimes of light transport that imitate either a multimode or a multicore fiber. The M3CF has been specifically designed for use in the initial phase of an in-vivo experiment, allowing for the navigation of the endoscope's distal end toward the targeted brain structure. The multicore regime enables the transfer of light to and from each individual neuron within the field of view. For chronic experiments in awake behaving mice, it is crucial to allow for disconnecting the fiber and the animal between experiments. Therefore, we provide here an effective solution and establish a protocol for reconnection of two segments of M3CF with hexagonally arranged corelets. RESULTS: We successfully utilized the M3CF to image neurons in anaesthetized transgenic mice expressing enhanced green fluorescent protein. Additionally, we compared imaging results obtained with the M3CF with larger numerical aperture (NA) fibers in fixed whole-brain tissue. CONCLUSIONS: This study focuses on addressing challenges and providing insights into the use of multimode-multicore fibers as imaging solutions for in-vivo applications. We suggest that the upcoming version of the M3CF increases the overall NA between the two cladding layers to allow for access to high resolution spatial imaging. As the NA increases in the multimode regime, the fiber diameter and ring structure must be reduced to minimize the computational burden and invasiveness.
- 590 __
- $a NEINDEXOVÁNO
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Dylda, Evelyn $u Otto-von-Guericke-University Magdeburg, Institute of Cognitive Neurology and Dementia Research, Magdeburg, Germany $u Center for Behavioral Brain Sciences, Magdeburg, Germany $1 https://orcid.org/0000000218834498
- 700 1_
- $a Stibůrek, Miroslav $u Institute of Scientific Instruments of CAS, Brno, Czechia $1 https://orcid.org/0000000240746080
- 700 1_
- $a Gomes, André D $u Leibniz Institute of Photonic Technology, Jena, Germany $1 https://orcid.org/0000000335123687
- 700 1_
- $a Turtaev, Sergey $u Leibniz Institute of Photonic Technology, Jena, Germany
- 700 1_
- $a Pakan, Janelle M P $u Otto-von-Guericke-University Magdeburg, Institute of Cognitive Neurology and Dementia Research, Magdeburg, Germany $u Center for Behavioral Brain Sciences, Magdeburg, Germany $u German Centre for Neurodegenerative Diseases, Magdeburg, Germany $u Leibniz Institute for Neurobiology, Magdeburg, Germany $1 https://orcid.org/0000000193848067
- 700 1_
- $a Čižmár, Tomáš $u Leibniz Institute of Photonic Technology, Jena, Germany $u Institute of Scientific Instruments of CAS, Brno, Czechia $u Friedrich Schiller University Jena, Institute of Applied Optics, Jena, Germany $1 https://orcid.org/0000000258133602
- 773 0_
- $w MED00209363 $t Neurophotonics $x 2329-423X $g Roč. 11, Suppl 1 (2024), s. S11506
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/38352728 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y - $z 0
- 990 __
- $a 20240405 $b ABA008
- 991 __
- $a 20240412130927 $b ABA008
- 999 __
- $a ok $b bmc $g 2075932 $s 1215259
- BAS __
- $a 3
- BAS __
- $a PreBMC-PubMed-not-MEDLINE
- BMC __
- $a 2024 $b 11 $c Suppl 1 $d S11506 $e 20240213 $i 2329-423X $m Neurophotonics $n Neurophotonics $x MED00209363
- LZP __
- $a Pubmed-20240405