In vitro monitoring of HTR2A-positive neurons derived from human-induced pluripotent stem cells.

Autor: Nakai K; Department of Prosthodontics, School of Dentistry, Showa University, 2-1-1 Kitasenzoku, Ohta-ku, Tokyo, 145-8515, Japan., Shiga T; Center for Genomic and Regenerative Medicine, School of Medicine, Juntendo University, 2-1-1 Hongo, Bunkyo-ku, 113-8421, Japan., Yasuhara R; Division of Pathology, Department of Oral Diagnostic Sciences, School of Dentistry, Showa University, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo, 142-8555, Japan., Sarkar AK; Department of Prosthodontics, School of Dentistry, Showa University, 2-1-1 Kitasenzoku, Ohta-ku, Tokyo, 145-8515, Japan., Abe Y; Department of Prosthodontics, School of Dentistry, Showa University, 2-1-1 Kitasenzoku, Ohta-ku, Tokyo, 145-8515, Japan., Nakamura S; Department of Oral Physiology, School of Dentistry, Showa University, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo, 142-8555, Japan., Hoashi Y; Department of Prosthodontics, School of Dentistry, Showa University, 2-1-1 Kitasenzoku, Ohta-ku, Tokyo, 145-8515, Japan., Kotani K; Department of Prosthodontics, School of Dentistry, Showa University, 2-1-1 Kitasenzoku, Ohta-ku, Tokyo, 145-8515, Japan., Tatsumoto S; Exploratory Research Center on Life and Living Systems (ExCELLS), National Institutes of Natural Science, 38 Nishigonaka, Myodaiji, Okazaki-shi, Aichi, 444-8585, Japan., Ishikawa H; Exploratory Research Center on Life and Living Systems (ExCELLS), National Institutes of Natural Science, 38 Nishigonaka, Myodaiji, Okazaki-shi, Aichi, 444-8585, Japan., Go Y; Exploratory Research Center on Life and Living Systems (ExCELLS), National Institutes of Natural Science, 38 Nishigonaka, Myodaiji, Okazaki-shi, Aichi, 444-8585, Japan.; Department of System Neuroscience, National Institute for Physiological Science, 38 Nishigonaka, Myodaiji, Okazaki-shi, Aichi, 444-8585, Japan.; Department of Physiological Science, School of Life Science, SOKENDAI (The Graduate University for Advanced Studies), 38 Nishigonaka, Myodaiji, Okazaki-shi, Aichi, 444-8585, Japan., Inoue T; Department of Oral Physiology, School of Dentistry, Showa University, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo, 142-8555, Japan., Mishima K; Division of Pathology, Department of Oral Diagnostic Sciences, School of Dentistry, Showa University, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo, 142-8555, Japan., Akamatsu W; Center for Genomic and Regenerative Medicine, School of Medicine, Juntendo University, 2-1-1 Hongo, Bunkyo-ku, 113-8421, Japan., Baba K; Department of Prosthodontics, School of Dentistry, Showa University, 2-1-1 Kitasenzoku, Ohta-ku, Tokyo, 145-8515, Japan. kazuyoshi@dent.showa-u.ac.jp.
Jazyk: angličtina
Zdroj: Scientific reports [Sci Rep] 2021 Jul 29; Vol. 11 (1), pp. 15437. Date of Electronic Publication: 2021 Jul 29.
DOI: 10.1038/s41598-021-95041-3
Abstrakt: The serotonin 5-HT 2A receptor (5-HT 2A R) has been receiving increasing attention because its genetic variants have been associated with a variety of neurological diseases. To elucidate the pathogenesis of the neurological diseases associated with 5-HT 2A R gene (HTR2A) variants, we have previously established a protocol to induce HTR2A-expressing neurons from human-induced pluripotent stem cells (hiPSCs). Here, we investigated the maturation stages and electrophysiological properties of HTR2A-positive neurons induced from hiPSCs and constructed an HTR2A promoter-specific reporter lentivirus to label the neurons. We found that neuronal maturity increased over time and that HTR2A expression was induced at the late stage of neuronal maturation. Furthermore, we demonstrated successful labelling of the HTR2A-positive neurons, which had fluorescence and generated repetitive action potentials in response to depolarizing currents and an inward current during the application of TCB-2, a selective agonist of 5-HT 2A Rs, respectively. These results indicated that our in vitro model mimicked the in vivo dynamics of 5-HT 2A R. Therefore, in vitro monitoring of the function of HTR2A-positive neurons induced from hiPSCs could help elucidate the pathophysiological mechanisms of neurological diseases associated with genetic variations of the HTR2A gene.
(© 2021. The Author(s).)
Databáze: MEDLINE
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