The goal of the proposed research is to develop a novel method of noninvasive light delivery for optogenetics. Successful completion of this project will enable us to perform functional mapping of the brain in vivo which will illuminate our understanding of the brain in new and exciting ways. The central obstacle to focusing light within tissue is the opacity of tissue in the optical regime. This opacity is mainly due to the strong scattering nature of tissue in the optical regime, which dwarfs the effects of absorption by 2-3 orders of magnitude. In much the same way as fog diffuses car headlights, tissue deflects incident light in a multitude of directions. If this scattering effect of tissue could be turned of, the human body would effectively behave as if it were translucent like a jellyfish. While this scattering may seem to be random, it is in fact a deterministic process. As a consequence of this fact, if the amplitude and phase of a light field exiting a scattering sample can be recorded and its optical phase conjugated wave back-propagated into the sample, the optical phase conjugated (OPC) wave will retrace the path of the original wave and reproduce the original light field. Prof. Yang's group has been developing a technology to exploit this discovery called digital time- reversed, ultrasound encoded light delivery (TRUE). This approach records the scattered light field and back-propagates the wave into the sample using an ultrasound focus at a point within the tissue to target a specific voxel. This technique has been demonstrated at depths up to 4 mm. My proposed project will continue to develop this technology to improve its maximum working depth and efficiency so that it can be used to activate or inhibit neurons within the brain using optogenetics. This challenging goal will be accomplished through three specific aims: (1) Improve the response time of the system to adequately adapt to changes in live tissue, (2) Convert the system from the current transmission based system to a reflection geometry to enable noninvasive operation, and (3) Test and optimize the digital TRUE system first using embedded fluorescent microbeads in rodent brain slices and finally activating specific neurons in the brain to demonstrate the feasibility of this technology for optogenetics in vivo. Successful completion of these goals will serve as a powerful demonstration of the capabilities of the digital TRUE system and enable functional brain mapping in vivo in a way that has never before been possible.

Public Health Relevance

In the rapidly evolving field of optogenetics, one of the major challenges to stimulating neurons deep within the brain in vivo is the strong scattering nature of tissue. The proposed research project will develop a method to noninvasively focus light on specific neurons deep in the brain using a technology called digital TRUE. This will enable functional brain mapping in vivo and open doors to new exploration in the brain.

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
5F31EB021153-02
Application #
9124597
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Erim, Zeynep
Project Start
2015-09-16
Project End
2017-11-10
Budget Start
2016-11-11
Budget End
2017-11-10
Support Year
2
Fiscal Year
2017
Total Cost
Indirect Cost
Name
California Institute of Technology
Department
Engineering (All Types)
Type
Biomed Engr/Col Engr/Engr Sta
DUNS #
009584210
City
Pasadena
State
CA
Country
United States
Zip Code
91125
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Ruan, Haowen; Haber, Tom; Liu, Yan et al. (2017) Focusing light inside scattering media with magnetic-particle-guided wavefront shaping. Optica 4:1337-1343
Brake, Joshua; Jang, Mooseok; Yang, Changhuei (2016) Analyzing the relationship between decorrelation time and tissue thickness in acute rat brain slices using multispeckle diffusing wave spectroscopy. J Opt Soc Am A Opt Image Sci Vis 33:270-5
Zhou, Edward Haojiang; Shibukawa, Atsushi; Brake, Joshua et al. (2016) Glare suppression by coherence gated negation. Optica 3:1107-1113