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1000 Titel
  • Advancing the path to in-vivo imaging in freely moving mice via multimode-multicore fiber based holographic endoscopy
1000 Autor/in
  1. Du, Yang |
  2. Dylda, Evelyn |
  3. Stibůrek, Miroslav |
  4. Gomes, André |
  5. Turtaev, Sergey |
  6. Pakan, Janelle |
  7. Cizmar, Tomas |
1000 Erscheinungsjahr 2024
1000 LeibnizOpen
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2024-02-13
1000 Erschienen in
1000 Quellenangabe
  • 11(Suppl 1):S11506
1000 FRL-Sammlung
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1117/1.NPh.11.S1.S11506 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10863504/ |
1000 Ergänzendes Material
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10863504/# |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • 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 M3CFwith 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.
1000 Sacherschließung
lokal freely moving
lokal holographic endoscopy
lokal multicore fiber
lokal multimode fiber
lokal in-vivo imaging
lokal fiber connection
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/RHUsIFlhbmc=|https://frl.publisso.de/adhoc/uri/RHlsZGEsIEV2ZWx5bg==|https://orcid.org/0000-0002-4074-6080|https://orcid.org/0000-0003-3512-3687|https://frl.publisso.de/adhoc/uri/VHVydGFldiwgU2VyZ2V5|https://orcid.org/0000-0001-9384-8067|https://orcid.org/0000-0002-5813-3602
1000 Label
1000 Förderer
  1. HORIZON EUROPE European Research Council |
  2. Ministerstvo Školství, Mládeže a Tělovýchovy |
  3. Thüringer Ministerium für Wirtschaft, Wissenschaft und Digitale Gesellschaft |
  4. Bundesministerium für Bildung und Forschung |
  5. Thüringer Aufbaubank |
  6. European Regional Development Fund |
  7. Natural Science Foundation of Hangzhou |
  8. Hangzhou Institute for Advanced Study, UCAS |
1000 Fördernummer
  1. 724530; 101069245; 101082088
  2. CZ.02.1.01/0.0/15_003/0000476
  3. -
  4. -
  5. -
  6. ZS/2016/04/78113
  7. LHZY24F030002
  8. -
1000 Förderprogramm
  1. -
  2. -
  3. -
  4. -
  5. -
  6. Center for Behavioral Brain Sciences
  7. -
  8. -
1000 Dateien
1000 Förderung
  1. 1000 joinedFunding-child
    1000 Förderer HORIZON EUROPE European Research Council |
    1000 Förderprogramm -
    1000 Fördernummer 724530; 101069245; 101082088
  2. 1000 joinedFunding-child
    1000 Förderer Ministerstvo Školství, Mládeže a Tělovýchovy |
    1000 Förderprogramm -
    1000 Fördernummer CZ.02.1.01/0.0/15_003/0000476
  3. 1000 joinedFunding-child
    1000 Förderer Thüringer Ministerium für Wirtschaft, Wissenschaft und Digitale Gesellschaft |
    1000 Förderprogramm -
    1000 Fördernummer -
  4. 1000 joinedFunding-child
    1000 Förderer Bundesministerium für Bildung und Forschung |
    1000 Förderprogramm -
    1000 Fördernummer -
  5. 1000 joinedFunding-child
    1000 Förderer Thüringer Aufbaubank |
    1000 Förderprogramm -
    1000 Fördernummer -
  6. 1000 joinedFunding-child
    1000 Förderer European Regional Development Fund |
    1000 Förderprogramm Center for Behavioral Brain Sciences
    1000 Fördernummer ZS/2016/04/78113
  7. 1000 joinedFunding-child
    1000 Förderer Natural Science Foundation of Hangzhou |
    1000 Förderprogramm -
    1000 Fördernummer LHZY24F030002
  8. 1000 joinedFunding-child
    1000 Förderer Hangzhou Institute for Advanced Study, UCAS |
    1000 Förderprogramm -
    1000 Fördernummer -
1000 Objektart article
1000 Beschrieben durch
1000 @id frl:6473247.rdf
1000 Erstellt am 2024-02-22T10:42:16.715+0100
1000 Erstellt von 242
1000 beschreibt frl:6473247
1000 Bearbeitet von 317
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1000 Objekt bearb. Fri Apr 12 07:12:35 CEST 2024
1000 Vgl. frl:6473247
1000 Oai Id
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1000 Sichtbarkeit Metadaten public
1000 Sichtbarkeit Daten public
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