Multimodal Imaging for DREADD-Expressing Neurons in Living Brain and Their Application to Implantation of iPSC-Derived Neural Progenitors.
Bin JiHiroyuki KanekoTakafumi MinanimotoHaruhisa InoueHiroki TakeuchiKatsushi KumataMing-Rong ZhangIchio AokiChie SekiMaiko OnoMasaki TokunagaSatoshi TsukamotoKoji TanabeRyong-Moon ShinTakeharu MinamihisamatsuSeiji KitoBarry J RichmondTetsuya SuharaMakoto HiguchiPublished in: The Journal of neuroscience : the official journal of the Society for Neuroscience (2017)
The present work provides the first successful demonstration of in vivo positron emission tomographic (PET) visualization of a chemogenetic designer receptor (designer receptor exclusively activated by designer drugs, DREADD) expressed in living brains. This technology has been applied to longitudinal PET reporter imaging of neuronal grafts differentiated from induced pluripotent stem cells. Differentiated from currently used reporter genes for neuroimaging, DREADD has also been available for functional manipulation of target cells, which could be visualized by functional magnetic resonance imaging (fMRI) in a real-time manner. Multimodal imaging with PET/fMRI enables the visualization of the differentiation of iPSC-derived neural progenitors into mature neurons and DREADD-mediated functional manipulation along the time course of the graft and is accordingly capable of fortifying the utility of stem cells in cell replacement therapies.
Keyphrases
- induced pluripotent stem cells
- resting state
- stem cells
- high resolution
- magnetic resonance imaging
- computed tomography
- functional connectivity
- positron emission tomography
- pet ct
- spinal cord
- crispr cas
- induced apoptosis
- pet imaging
- single cell
- pain management
- white matter
- cell death
- spinal cord injury
- multiple sclerosis
- cell cycle arrest
- genome wide
- mass spectrometry
- oxidative stress
- chronic pain
- bone marrow
- magnetic resonance