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Extended field-of-view ultrathin microendoscopes for high-resolution two-photon imaging with minimal invasiveness.
Antonini, Andrea; Sattin, Andrea; Moroni, Monica; Bovetti, Serena; Moretti, Claudio; Succol, Francesca; Forli, Angelo; Vecchia, Dania; Rajamanickam, Vijayakumar P; Bertoncini, Andrea; Panzeri, Stefano; Liberale, Carlo; Fellin, Tommaso.
Afiliação
  • Antonini A; Optical Approaches to Brain Function Laboratory, Istituto Italiano di Tecnologia, Genova, Italy.
  • Sattin A; Nanostructures Department, Istituto Italiano di Tecnologia, Genova, Italy.
  • Moroni M; Optical Approaches to Brain Function Laboratory, Istituto Italiano di Tecnologia, Genova, Italy.
  • Bovetti S; University of Genova, Genova, Italy.
  • Moretti C; Neural Coding Laboratory, Istituto Italiano di Tecnologia, Genova and Rovereto, Italy.
  • Succol F; Neural Coding Laboratory, Istituto Italiano di Tecnologia, Genova and Rovereto, Italy.
  • Forli A; Neural Computation Laboratory, Center for Neuroscience and Cognitive Systems @UniTn, Istituto Italiano di Tecnologia, Rovereto, Italy.
  • Vecchia D; Center for Mind and Brain Sciences (CIMeC), University of Trento, Rovereto, Italy.
  • Rajamanickam VP; Optical Approaches to Brain Function Laboratory, Istituto Italiano di Tecnologia, Genova, Italy.
  • Bertoncini A; Optical Approaches to Brain Function Laboratory, Istituto Italiano di Tecnologia, Genova, Italy.
  • Panzeri S; University of Genova, Genova, Italy.
  • Liberale C; Optical Approaches to Brain Function Laboratory, Istituto Italiano di Tecnologia, Genova, Italy.
  • Fellin T; Optical Approaches to Brain Function Laboratory, Istituto Italiano di Tecnologia, Genova, Italy.
Elife ; 92020 10 13.
Article em En | MEDLINE | ID: mdl-33048047
ABSTRACT
Imaging neuronal activity with high and homogeneous spatial resolution across the field-of-view (FOV) and limited invasiveness in deep brain regions is fundamental for the progress of neuroscience, yet is a major technical challenge. We achieved this goal by correcting optical aberrations in gradient index lens-based ultrathin (≤500 µm) microendoscopes using aspheric microlenses generated through 3D-microprinting. Corrected microendoscopes had extended FOV (eFOV) with homogeneous spatial resolution for two-photon fluorescence imaging and required no modification of the optical set-up. Synthetic calcium imaging data showed that, compared to uncorrected endoscopes, eFOV-microendoscopes led to improved signal-to-noise ratio and more precise evaluation of correlated neuronal activity. We experimentally validated these predictions in awake head-fixed mice. Moreover, using eFOV-microendoscopes we demonstrated cell-specific encoding of behavioral state-dependent information in distributed functional subnetworks in a primary somatosensory thalamic nucleus. eFOV-microendoscopes are, therefore, small-cross-section ready-to-use tools for deep two-photon functional imaging with unprecedentedly high and homogeneous spatial resolution.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tálamo / Microscopia de Fluorescência por Excitação Multifotônica Tipo de estudo: Evaluation_studies Limite: Animals Idioma: En Revista: Elife Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tálamo / Microscopia de Fluorescência por Excitação Multifotônica Tipo de estudo: Evaluation_studies Limite: Animals Idioma: En Revista: Elife Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Itália