Author:
Okamoto Kazuki,Kamikubo Yuji,Yamauchi Kenta,Okamoto Shinichiro,Takahashi Megumu,Ishida Yoko,Koike Masato,Ikegaya Yuji,Sakurai Takashi,Hioki Hiroyuki
Abstract
AbstractGiven its limited accessibility, the CA2 area has been less investigated compared to other subregions of the hippocampus. While the development of transgenic mice expressing Cre recombinase in the CA2 has revealed unique features of this area, the use of mouse lines has several limitations, such as lack of specificity. Therefore, a specific gene delivery system is required. Here, we confirmed that the AAV-PHP.eB capsid preferably infected CA2 pyramidal cells following retro-orbital injection and demonstrated that the specificity was substantially higher after injection into the lateral ventricle. In addition, a tropism for the CA2 area was observed in organotypic slice cultures. Combined injection into the lateral ventricle and stereotaxic injection into the CA2 area specifically introduced the transgene into CA2 pyramidal cells, enabling us to perform targeted patch-clamp recordings and optogenetic manipulation. These results suggest that AAV-PHP.eB is a versatile tool for specific gene transduction in CA2 pyramidal cells.
Funder
Japan Society for the Promotion of Science
Research Institute for Diseases of Old Age, Juntendo University School of Medicine
Research Institute for Diseases of Old Age,Juntendo University School of Medicine
Japan Agency for Medical Research and Development
Japan Science and Technology Agency
Publisher
Springer Science and Business Media LLC