Hokkaido University · 신경과학
마사히코 와타나베 교수의 연구실은 신경전달물질 수용체와 신호전달 분자의 세포 및 세분적 분포를 분석함으로써 뇌 기능의 분자 기반을 규명하는 데 초점을 맞추고 있습니다. 특히 NMDA 수용체, 엔도칸나비노이드 수용체, 아세틸콜린 수용체 등 주요 신호전달 수용체의 발현 패tern과 그 기능적 의미를 유전자위치화 및 전자현미경 기법을 통해 탐색하고 있습니다. 연구는 뇌 발달 과정에서 수용체의 발현 변화와 시냅스 전후 신호전달 메커니즘의 기초를 규명하는 데 기여하고 있습니다.
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
In situ hybridization analyses have revealed drastic changes in expression and distribution of five subunit mRNAs of the mouse NMDA receptor channel during brain development. The epsilon 1 subunit mRNA is expressed postnatally and widely in the brain. On the other hand, the epsilon 2 subunit mRNA is found throughout the entire embryonic brain, but its expression becomes restricted to the forebrain at postnatal stages. The epsilon 3 subunit mRNA appears postnatally and predominantly in the cerebe
2-arachidonoyl-glycerol (2-AG) is an endocannabinoid that is released from postsynaptic neurons, acts retrogradely on presynaptic cannabinoid receptor CB1, and induces short- and long-term suppression of transmitter release. To understand the mechanisms of the 2-AG-mediated retrograde modulation, we investigated subcellular localization of a major 2-AG biosynthetic enzyme, diacylglycerol lipase-alpha (DAGLalpha), by using immunofluorescence and immunoelectron microscopy in the mouse brain. In th
Abstract The distributions of five NMDA receptor channel subunit mRNAs in the mouse forebrain at postnatal day 21 were semiquantitatively examined by in situ hybridization with subunit‐specific oligonucleotide probes. In contrast to ubiquitous distribution of the ζ1 subunit mRNA throughout the forebrain, distributions of four ϵ subunit mRNAs were highly variable from nucleus to nucleus. The telencephalon (except for the septum) expressed the ϵ1 and ϵ2 subunit mRNAs. Various combinations of the ϵ
Acetylcholine (ACh) plays important roles for higher brain functions, including arousal, attention, and cognition. These effects are mediated largely by muscarinic acetylcholine receptors (mAChRs). However, it remains inconclusive whether the mode of ACh-mAChR signaling is synaptic, so-called "wired," transmission mediated by ACh released into the synaptic cleft, or nonsynaptic, so-called "volume," transmission by ambient ACh. To address this issue, we examined cellular and subcellular distribut