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  MRI-guided robotic arm drives optogenetic fMRI with concurrent Ca2+ recording

Chen, Y., Pais-Roldán, P., Chen, X., Frosz, M., & Yu, X. (2019). MRI-guided robotic arm drives optogenetic fMRI with concurrent Ca2+ recording. Nature Communications, 10(1): 2536, pp. 1-11. doi:10.1038/s41467-019-10450-3.

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Chen, Y1, Author
Pais-Roldán, P1, Author
Chen, X1, Author
Frosz, Michael2, 3, Author           
Yu, X1, Author
Affiliations:
1external, ou_persistent22              
2Russell Division, Max Planck Institute for the Science of Light, Max Planck Society, ou_2364721              
3Fibre Fabrication and Glass Studio, Technology Development and Service Units, Max Planck Institute for the Science of Light, Max Planck Society, Staudtstraße 2, 91058 Erlangen, DE, ou_2364724              

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 Abstract: Optical fiber-mediated optogenetic activation and neuronal Ca2+ recording in combination with fMRI provide a multi-modal fMRI platform. Here, we developed an MRI-guided robotic arm (MgRA) as a flexible positioning system with high precision to real-time assist optical fiber brain intervention for multi-modal animal fMRI. Besides the ex vivo precision evaluation, we present the highly reliable brain activity patterns in the projected basal forebrain regions upon MgRA-driven optogenetic stimulation in the lateral hypothalamus. Also, we show the step-wise optical fiber targeting thalamic nuclei and map the region-specific functional connectivity with whole-brain fMRI accompanied by simultaneous calcium recordings to specify its circuit-specificity. The MgRA also guides the real-time microinjection to specific deep brain nuclei, which is demonstrated by an Mn-enhanced MRI method. The MgRA represents a clear advantage over the standard stereotaxic-based fiber implantation and opens a broad avenue to investigate the circuit-specific functional brain mapping with the multi-modal fMRI platform.

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 Dates: 2019-06
 Publication Status: Published online
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 Identifiers: DOI: 10.1038/s41467-019-10450-3
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Title: Nature Communications
  Abbreviation : Nat. Commun.
Source Genre: Journal
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Publ. Info: London : Nature Publishing Group
Pages: - Volume / Issue: 10 (1) Sequence Number: 2536 Start / End Page: 1 - 11 Identifier: ISSN: 2041-1723
CoNE: https://pure.mpg.de/cone/journals/resource/2041-1723