TY - JOUR
T1 - Multimodal imaging for DREADD-expressing neurons in living brain and their application to implantation of iPSC-derived neural progenitors
AU - Ji, Bin
AU - Kaneko, Hiroyuki
AU - Minamimoto, Takafumi
AU - Inoue, Haruhisa
AU - Takeuchi, Hiroki
AU - Kumata, Katsushi
AU - Zhang, Ming Rong
AU - Aoki, Ichio
AU - Seki, Chie
AU - Ono, Maiko
AU - Tokunaga, Masaki
AU - Tsukamoto, Satoshi
AU - Tanabe, Koji
AU - Shin, Ryong Moon
AU - Minamihisamatsu, Takeharu
AU - Kito, Seiji
AU - Richmond, Barry J.
AU - Suhara, Tetsuya
AU - Higuchi, Makoto
N1 - Publisher Copyright:
© 2016 the authors.
PY - 2016/11/9
Y1 - 2016/11/9
N2 - Chemogenetic manipulation of neuronal activities has been enabled by a designer receptor (designer receptor exclusively activated by designer drugs, DREADD) that is activated exclusively by clozapine-N-oxide (CNO). Here, we applied CNO as a functional reporter probe to positron emission tomography (PET) of DREADD in living brains. Mutant human M4 DREADD (hM4Di) expressed in transgenic (Tg) mouse neurons was visualized by PET with microdose [11C]CNO. Deactivation of DREADD-expressing neurons in these mice by nonradioactive CNO at a pharmacological dose could also be captured by arterial spin labeling MRI (ASL-MRI). Neural progenitors derived from hM4Di Tg-induced pluripotent stem cells were then implanted into WT mouse brains and neuronal differentiation of the grafts could be imaged by [11C]CNO-PET. Finally, ASL-MRI captured chemogenetic functional manipulation of the graft neurons. Our data provide the first demonstration of multimodal molecular/functional imaging of cells expressing a functional gene reporter in the brain, which would be translatable to humans for therapeutic gene transfers and cell replacements.
AB - Chemogenetic manipulation of neuronal activities has been enabled by a designer receptor (designer receptor exclusively activated by designer drugs, DREADD) that is activated exclusively by clozapine-N-oxide (CNO). Here, we applied CNO as a functional reporter probe to positron emission tomography (PET) of DREADD in living brains. Mutant human M4 DREADD (hM4Di) expressed in transgenic (Tg) mouse neurons was visualized by PET with microdose [11C]CNO. Deactivation of DREADD-expressing neurons in these mice by nonradioactive CNO at a pharmacological dose could also be captured by arterial spin labeling MRI (ASL-MRI). Neural progenitors derived from hM4Di Tg-induced pluripotent stem cells were then implanted into WT mouse brains and neuronal differentiation of the grafts could be imaged by [11C]CNO-PET. Finally, ASL-MRI captured chemogenetic functional manipulation of the graft neurons. Our data provide the first demonstration of multimodal molecular/functional imaging of cells expressing a functional gene reporter in the brain, which would be translatable to humans for therapeutic gene transfers and cell replacements.
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U2 - 10.1523/JNEUROSCI.1279-16.2016
DO - 10.1523/JNEUROSCI.1279-16.2016
M3 - Article
C2 - 27911758
AN - SCOPUS:84994715846
SN - 0270-6474
VL - 36
SP - 11544
EP - 11558
JO - Journal of Neuroscience
JF - Journal of Neuroscience
IS - 45
ER -