Abstract: This proposal suggests a consilience of bold new concepts in genetics, stem cell biology, and functional magnetic resonance imaging (fMRI) to address a singular question that could never be tapped previously: can we directly map the functionality of stem cell-driven neural circuit regeneration in vivo? Despite the debilitating character of central nervous system (CNS) diseases, and the urgency for therapeutic development, the complex nature of the neural fabric underlying CNS diseases such as spinal cord injuries, Parkinson's disease, Alzheimer's disease, multiple sclerosis, and stroke, substantially negate their viable cure to date. Here, the fundamental ability of stem cells to regenerate non-dividing cells, as well as recent development of induced pluripotent stem cells (IPSC) gives fresh impetus for a whole new class of innovative treatments where damaged neural circuitry might be partially or fully restored by stem-cell induced neurogenesis. We seek to be instrumental in this pivotal endeavor by introducing a completely novel way of directly assessing the functionality of stem cell driven neural circuitry in vivo. This will be achieved by combining genetic techniques that will introduce modulatory and/or reporting capability to neural cells based on its cell type. We will strategically introduce viral vectors to both the underlying neural circuit as well as transplanted stem cells. For stem cell transfection, we expect our proposed technique to allow modulatory/reporting capability from only those developing into specific cell types. This cell-specific modulation/reporting capability will then combined with a novel distortion-free fMRI imaging technique, permitting non-invasive and high-resolution visualization of the regeneration processes. This project, upon its success, will provide direct functional assessment capabilities for the regenerated nerve tissue in vivo. This in turn will provide key guidance for developing novel stem cell therapies for CNS diseases. Public Health Relevance: The complexity and functional nature of neural circuitry makes central nervous systems (CNS) diseases such as spinal cord injuries, Parkinson's disease, Alzheimer's disease, multiple sclerosis, and stroke particularly challenging for therapeutic approaches. While recent development of induced pluripotent stem cells (IPSC) gives fresh impetus for a whole new class of innovative treatment landscapes for patients with debilitating CNS diseases, the ultimate functionality of stem cell induced CNS regeneration remains elusive. This project, upon its success, will provide direct and functional assessment capabilities for the regenerated nerve tissue in vivo. This in turn will provide key guidance for developing novel stem cell therapies for CNS diseases.

Agency
National Institute of Health (NIH)
Institute
Office of The Director, National Institutes of Health (OD)
Type
NIH Director’s New Innovator Awards (DP2)
Project #
1DP2OD007265-01
Application #
7981828
Study Section
Special Emphasis Panel (ZGM1-NDIA-O (01))
Program Officer
Basavappa, Ravi
Project Start
2010-09-30
Project End
2012-06-30
Budget Start
2010-09-30
Budget End
2012-06-30
Support Year
1
Fiscal Year
2010
Total Cost
$156,124
Indirect Cost
Name
University of California Los Angeles
Department
Type
Schools of Medicine
DUNS #
092530369
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Choy, ManKin; Duffy, Ben A; Lee, Jin Hyung (2017) Optogenetic study of networks in epilepsy. J Neurosci Res 95:2325-2335
Liu, Jia; Duffy, Ben A; Bernal-Casas, David et al. (2017) Comparison of fMRI analysis methods for heterogeneous BOLD responses in block design studies. Neuroimage 147:390-408
Bernal-Casas, David; Lee, Hyun Joo; Weitz, Andrew J et al. (2017) Studying Brain Circuit Function with Dynamic Causal Modeling for Optogenetic fMRI. Neuron 93:522-532.e5
Fang, Zhongnan; Van Le, Nguyen; Choy, ManKin et al. (2016) High spatial resolution compressed sensing (HSPARSE) functional MRI. Magn Reson Med 76:440-55
Lee, Hyun Joo; Weitz, Andrew J; Bernal-Casas, David et al. (2016) Activation of Direct and Indirect Pathway Medium Spiny Neurons Drives Distinct Brain-wide Responses. Neuron 91:412-24
Lin, Peter; Fang, Zhongnan; Liu, Jia et al. (2016) Optogenetic Functional MRI. J Vis Exp :
Byers, Blake; Lee, Hyun Joo; Liu, Jia et al. (2015) Direct in vivo assessment of human stem cell graft-host neural circuits. Neuroimage 114:328-37
Weitz, Andrew J; Fang, Zhongnan; Lee, Hyun Joo et al. (2015) Optogenetic fMRI reveals distinct, frequency-dependent networks recruited by dorsal and intermediate hippocampus stimulations. Neuroimage 107:229-41
Duffy, Ben A; Choy, ManKin; Chuapoco, Miguel R et al. (2015) MRI compatible optrodes for simultaneous LFP and optogenetic fMRI investigation of seizure-like afterdischarges. Neuroimage 123:173-84
Pashaie, Ramin; Anikeeva, Polina; Lee, Jin Hyung et al. (2014) Optogenetic brain interfaces. IEEE Rev Biomed Eng 7:3-30

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