All

What are you looking for?

All
Projects
Results
Organizations

Quick search

  • Projects supported by TA ČR
  • Excellent projects
  • Projects with the highest public support
  • Current projects

Smart search

  • That is how I find a specific +word
  • That is how I leave the -word out of the results
  • “That is how I can find the whole phrase”

Subcellular spatial resolution achieved for deep-brain imaging in vivo using a minimally invasive multimode fiber

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68081731%3A_____%2F18%3A00499922" target="_blank" >RIV/68081731:_____/18:00499922 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1038/s41377-018-0111-0" target="_blank" >http://dx.doi.org/10.1038/s41377-018-0111-0</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1038/s41377-018-0111-0" target="_blank" >10.1038/s41377-018-0111-0</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Subcellular spatial resolution achieved for deep-brain imaging in vivo using a minimally invasive multimode fiber

  • Original language description

    Achieving intravital optical imaging with diffraction-limited spatial resolution of deep-brain structures represents an important step toward the goal of understanding the mammalian central nervous system(1-4). Advances in wavefront-shaping methods and computational power have recently allowed for a novel approach to high-resolution imaging, utilizing deterministic light propagation through optically complex media and, of particular importance for this work, multimode optical fibers (MMFs)(5-7). We report a compact and highly optimized approach for minimally invasive in vivo brain imaging applications. The volume of tissue lesion was reduced by more than 100-fold, while preserving diffraction-limited imaging performance utilizing wavefront control of light propagation through a single 50-mu m-core MMF. Here, we demonstrated high-resolution fluorescence imaging of subcellular neuronal structures, dendrites and synaptic specializations, in deep-brain regions of living mice, as well as monitored stimulus-driven functional Ca2+ responses. These results represent a major breakthrough in the compromise between high-resolution imaging and tissue damage, heralding new possibilities for deep-brain imaging in vivo.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10306 - Optics (including laser optics and quantum optics)

Result continuities

  • Project

    <a href="/en/project/EF15_003%2F0000476" target="_blank" >EF15_003/0000476: Holographic endoscopy for in vivo applications</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2018

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Light-Science & Applications

  • ISSN

    2047-7538

  • e-ISSN

  • Volume of the periodical

    7

  • Issue of the periodical within the volume

    DEC

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    6

  • Pages from-to

  • UT code for WoS article

    000453577600002

  • EID of the result in the Scopus database

    2-s2.0-85058859483