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Transgenic Expression of Enhanced Green Fluorescent Protein Enables Direct Visualization for Physiological Studies of Vasopressin Neurons and Isolated Nerve Terminals of the Rat
Author(s) -
Yoichi Ueta,
Hiroaki Fujihara,
Ryota Serino,
Govindan Dayanithi,
Hitoshi Ozawa,
Kenichi Matsuda,
Mitsuhiro Kawata,
Junko Yamada,
Shinya Ueno,
Atsuo Fukuda,
David Murphy
Publication year - 2004
Publication title -
endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.674
H-Index - 257
eISSN - 1945-7170
pISSN - 0013-7227
DOI - 10.1210/en.2004-0830
Subject(s) - vasopressin , supraoptic nucleus , green fluorescent protein , suprachiasmatic nucleus , biology , medicine , axon , endocrinology , nucleus , transgene , microbiology and biotechnology , hypothalamus , neuropeptide , gene , receptor , biochemistry
We have generated transgenic rats expressing an arginine vasopressin (AVP)-enhanced green fluorescent protein (eGFP) fusion gene. The expression of the eGFP gene and strong fluorescence were observed in the supraoptic nucleus (SON), the paraventricular nucleus (PVN), and the suprachiasmatic nucleus (SCN) in transgenic rats. The hypothalamo-neurohypophyseal tract, isolated SON neurons, and isolated axon terminals in the neurohypophysis also showed robust eGFP fluorescence. Water deprivation for 2 d increased the fluorescence of the eGFP in the SON and the PVN but not the SCN. The whole-cell patch-clamp technique was then used to record the electrical activities specifically identifying eGFP-expressing SON, PVN, and SCN AVP neurons in in vitro brain slice preparations. The AVP-eGFP transgenic rats are a unique new tool with which to study the physiological role of AVP-secreting neurons in the central nervous system and the dynamics of the regulation of AVP secretion in the living neurons and their axon terminals.

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