January 2014 Fluorescent labeling of GABAergic neurons in the GAD67-GFP knock-in mouse

Fluorescent labeling of GABAergic neurons in the GAD67-GFP knock-in mouse

ICR.Cg-Gad1<tm1.1Tama>/Rbrc (RBRC03674)

Jan 2014 Fluorescent labeling of GABAergic neurons in the GAD67-GFP knock-in mouse

Courtesy of Yuchio Yanagawa, M.D.

Expression of EGFP in the GAD67-GFP knock-in mouse. (Left) Fluorescent photomicrograph of a sagittal section of the GAD67-GFP knock-in mouse brain (4 weeks old) shows scattered distribution of EGFP in the hippocampus and cerebral cortex. (Right) Fluorescent photomicrograph of a sagittal section of the GAD67-GFP knock-in mouse cerebellar cortex (4 weeks old). Arrowheads in the right panels show Golgi cells. Merged images include nuclear staining with DAPI (blue). CA1-3, CA1-3 fields of Ammon’s horn; DG, dentate gyrus; Gr, granule cell layer of cerebellar cortex; MO, molecular layer of cerebellar cortex; PC, Purkinje cell layer. Scale bars: left, 500 µm; right, 50 µm. Photographs were provided by Dr. Ryosuke Kaneko, Gunma University.

GABAergic neurons play an important role in the regulation and stabilization of network activities and are essential for a number of brain functions including cognition and emotion. Because GABAergic neurons are primarily scattered throughout the central nervous system, it is difficult to identify these cells in living brain preparations. A specific marker for GABAergic neurons is the enzyme glutamate decarboxylase 67 (GAD67). GAD67-GFP knock-in mice were generated using a gene targeting method via homologous recombination in embryonic stem cells [1, 2]. GFP fluorescence was observed specifically in the majority of GABAergic neurons in these knock-in mice, and these neurons could be detected easily by fluorescent microscopy without immunostaining. GAD67-GFP knock-in mice have facilitated the study of both the electrophysiological and anatomical profiles of GABAergic neurons [3-5].

Depositor	:	Yuchio Yanagawa, M.D. Department of Genetic and Behavioral Neuroscience Gunma University Graduate School of Medicine
References	:	[1]	Tamamaki N, Yanagawa Y, Tomioka R, Miyazaki J, Obata K, Kaneko T. Green fluorescent protein expression and colocalization with calretinin, parvalbumin, and somatostatin in the GAD67-GFP knock-in mouse. J Comp Neurol.; 467(1):60-79, 2003.
		[2]	Kaneko K, Tamamaki N, Owada H, Kakizaki T, Kume N, Totsuka M, Yamamoto T, Yawo H, Yagi T, Obata K, Yanagawa Y. Noradrenergic excitation of a subpopulation of GABAergic cells in the basolateral amygdala via both activation of nonselective cationic conductance and suppression of resting K⁺ conductance: A study using glutamate decarboxylase 67-green fluorescent protein knock-in mice. Neuroscience 157, 781-797, 2008.
		[3]	Brown RE, McKenna JT, Winston S, Basheer R, Yanagawa Y, Thakkar MM, McCarley RW. Characterization of GABAergic neurons in rapid-eye-movement sleep controlling regions of the brainstem reticular formation in GAD67-green fluorescent protein knock-in mice. Eur J Neurosci.; 27(2):352-63, 2008.
		[4]	Hirono M, Saitow F, Kudo M, Suzuki H, Yanagawa Y, Yamada M, Nagao S, Konishi S, Obata K. Cerebellar globular cells receive monoaminergic excitation and monosynaptic inhibition from Purkinje cells. PLoS One 7:e29663, 2012.
		[5]	Kawabata I, Kashiwagi Y, Obashi K, Ohkura M, Nakai J, Wynshaw-Boris A, Yanagawa Y, Okabe S. LIS1-dependent retrograde translocation of excitatory synapses in developing interneuron dendrites. Nat Commun. 3:722, 2012.

January 2014
Contact: Shinya Ayabe, Ph.D.
Experimental Animal Division, RIKEN BioResource Center
All materials contained on this site may not be reproduced, distributed, displayed, published or broadcast without the prior permission of the owner of that content.

コメントは受け付けていません。