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Project Summary To further our understanding of the function of neural circuits, there is a need for new tools that can collect simultaneous measurements from large populations of neurons involved in a common neural computation and provide precise functional modulation. Optical imaging in awake animals expressing calcium indicators provides real-time functional and spatial information from individual neurons within local neural circuits. The limitations of current imaging technology include small fields of view encompassing single brain regions, and the requirement for head fixation, which prevents naturalistic behavior. In addition, most optical imaging systems do not allow for simultaneous high-resolution functional imaging in combination with spatially-localized optogenetic modulation. To meet this challenge, we propose to develop an optical device (`3D-FAST') that allows for rapid, real-time volumetric neural recording and precise optical stimulation. By pairing miniature arrays of micropatterned LED emitters with the axial focusing capabilities of electrowetting lens technologies, we will achieve duplex recording and stimulation of many thousands of neurons. Through utilization of novel 3D-printed scaffolding, we will be able to create modular, expandable, customizable lens arrays that allow for recording of large-scale bi-directional neural interfaces for closed-loop modulation of neural circuits. We will create the 3D-FAST device through assembly of modular optical elements in a 3D-printed scaffolding. The initial device will be tested in in the anesthetized mouse during the presentation of visual stimuli. Optogenetic stimulation will be used to bias circuit function. In sum, these experiments will demonstrate the unique capabilities of the 3D-FAST technology. Rapid, high- resolution imaging of calcium transients from a volume of tissue will be paired with spatially-restricted light delivery for optogenetic neural modulation. The optical imaging properties will be compared with ground-truth two-photon microscopy, and the functional consequence of neuromodulation will be dissected through circuit modulation. The 3D-FAST tool will bring novel capabilities to measuring and modulating large populations of neurons in animals, to better understand the neural computations that underlie behavior. In addition, this body of work will lay the ground for future development of fully implantable optical recording and modulating units for use in freely-moving, untethered naturalistic behavior experiments.
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MicroLED light source for optical sectioning structured illumination microscopy
用于光学切片结构照明显微镜的 MicroLED 光源
DOI: 10.1364/oe.486754
发表时间: 2023
期刊: Optics Express
影响因子: 3.8
作者: [Kumar, Vikrant, Behrman, Keith, Speed, Forest, Saladrigas, Catherine A., Supekar, Omkar, Huang, Zicong, Bright, Victor M., Welle, Cristin G., Restrepo, Diego, Gopinath, Juliet T.]
通讯作者: Gopinath, Juliet T.
DOI: 10.1364/oe.425800
发表时间: 2021-05-10
期刊: OPTICS EXPRESS
影响因子: 3.8
作者: [Behrman, Keith, Kymissis, Ioannis]
通讯作者: Kymissis, Ioannis
Development of 3D-FAST Optical Interface for Rapid Volumetric Neural Sensing and Modulation
  • 批准号:
    10294019
  • 项目类别:
  • 资助金额:
    $266.58万
  • 财政年份:
    2021
  • 负责人:
    Emily Gibson
  • 依托单位:
Shedding light on brain circuits mediating navigation of the odor plume in a natural environment
  • 批准号:
    10241846
  • 项目类别:
  • 资助金额:
    $8.95万
  • 财政年份:
    2020
  • 负责人:
    Emily Gibson
  • 依托单位:
Shedding light on brain circuits mediating navigation of the odor plume in a natural environment
  • 批准号:
    10216476
  • 项目类别:
  • 资助金额:
    $27.18万
  • 财政年份:
    2020
  • 负责人:
    Emily Gibson
  • 依托单位:
Controlled neuronal firing in vivo using two photon spatially shaped optogenetics
  • 批准号:
    9770567
  • 项目类别:
  • 资助金额:
    $80.09万
  • 财政年份:
    2017
  • 负责人:
    Emily Gibson
  • 依托单位:
海外基金