Author:
Hirata Yoshihiro,Enoki Ryosuke,Kuribayashi-Shigetomi Kaori,Oda Yoshiaki,Honma Sato,Honma Ken-ichi
Abstract
AbstractCircadian rhythms in Per1, PER2 expression and intracellular Ca2+ were measured from a solitary SCN neuron or glial cell which was physically isolated from other cells. Dispersed cells were cultured on a platform of microisland (100–200 μm in diameter) in a culture dish. Significant circadian rhythms were detected in 57.1% for Per1 and 70.0% for PER2 expression. When two neurons were located on the same island, the circadian rhythms showed desynchronization, indicating a lack of oscillatory coupling. Circadian rhythms were also detected in intracellular Ca2+ of solitary SCN neurons. The ratio of circadian positive neurons was significantly larger without co-habitant of glial cells (84.4%) than with it (25.0%). A relatively large fraction of SCN neurons generates the intrinsic circadian oscillation without neural or humoral networks. In addition, glial cells seem to interrupt the expression of the circadian rhythmicity of intracellular Ca2+ under these conditions.
Funder
MEXT | Japan Society for the Promotion of Science
Research Foundation for Opto-Science and Technology, The Ichiro Kanehara Foundation
MEXT | JST | Precursory Research for Embryonic Science and Technology
Takeda Science Foundation, The Mochida memorial foundation, The Ichiro Kanehara Foundation, The Suhara Memorial Foundation, Uehara Memorial Foundation
The Cooperative Research Project for Advanced Photonic Bioimaging
Publisher
Springer Science and Business Media LLC
Cited by
12 articles.
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