Demonstration of functional coupling between γ-aminobutyric acid (GABA) synthesis and vesicular GABA transport into synaptic vesicles

被引:188
作者
Jin, H
Wu, H
Osterhaus, G
Wei, JN
Davis, K
Sha, D
Floor, E
Hsu, CC
Kopke, RD
Wu, JY [1 ]
机构
[1] Univ Kansas, Dept Mol Biosci, Lawrence, KS 66045 USA
[2] Univ Kansas, Dept Med Chem, Lawrence, KS 66045 USA
[3] Florida Atlantic Univ, Dept Biomed Sci, Boca Raton, FL 33431 USA
[4] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
[5] USN Med Ctr, Dept Otolaryngol, San Diego, CA 92134 USA
关键词
D O I
10.1073/pnas.0730698100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
L-Glutamic acid decarboxylase (GAD) exists as both membrane-associated and soluble forms in the mammalian brain. Here, we propose that there is a functional and structural coupling between the synthesis of gamma-aminobutyric acid (GABA) by membrane-associated GAD and its packaging into synaptic vesicles (SVs) by vesicular GABA transporter (VGAT): This notion is supported by the following observations. First, newly synthesized [H-3]GABA from [H-3]L-glutamate by membrane-associated GAD is taken up preferentially over preexisting GABA by using immunoaffinity-purified GABAergic SVs. Second, the activity of SV-associated GAD and VGAT seems to be coupled because inhibition of GAD also decreases VGAT activity. Third, VGAT and SV-associated Ca2+/ calmodulin-dependent kinase II have been found to form a protein complex with GAD. A model is also proposed to link the neuronal stimulation to enhanced synthesis and packaging of GABA into SVs.
引用
收藏
页码:4293 / 4298
页数:6
相关论文
共 33 条
[1]   SYNAPTIC VESICLES FROM HOG BRAIN THEIR ISOLATION AND THE COUPLING BETWEEN SYNTHESIS AND UPTAKE OF GAMMA-AMINOBUTYRATE BY GLUTAMATE-DECARBOXYLASE [J].
ANGEL, I ;
FLEISSNER, A ;
SEIFERT, R .
NEUROCHEMISTRY INTERNATIONAL, 1983, 5 (06) :697-712
[2]   Cleft palate and decreased brain gamma-aminobutyric acid in mice lacking the 67-kDa isoform of glutamic acid decarboxylase [J].
Asada, H ;
Kawamura, Y ;
Maruyama, K ;
Kume, H ;
Ding, RG ;
Kanbara, N ;
Kuzume, H ;
Sanbo, M ;
Yagi, T ;
Obata, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (12) :6496-6499
[3]   BRAIN L-GLUTAMATE DECARBOXYLASE - INHIBITION BY PHOSPHORYLATION AND ACTIVATION BY DEPHOSPHORYLATION [J].
BAO, J ;
CHEUNG, WY ;
WU, JY .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (12) :6464-6467
[4]  
CHANG YC, 1988, J NEUROSCI, V8, P2123
[5]  
Choi SY, 2002, J NEUROSCI, V22, P5271
[6]   MEMBRANE ANCHORING OF THE AUTOANTIGEN-GAD(65) TO MICROVESICLES IN PANCREATIC BETA-CELLS BY PALMITOYLATION IN THE NH2-TERMINAL DOMAIN [J].
CHRISTGAU, S ;
AANSTOOT, HJ ;
SCHIERBECK, H ;
BEGLEY, K ;
TULLIN, S ;
HEJNAES, K ;
BAEKKESKOV, S .
JOURNAL OF CELL BIOLOGY, 1992, 118 (02) :309-320
[7]   Cleft palate in mice with a targeted mutation in the gamma-aminobutyric acid-producing enzyme glutamic acid decarboxylase 67 [J].
Condie, BG ;
Bain, G ;
Gottlieb, DI ;
Capecchi, MR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (21) :11451-11455
[8]   A novel method for expression and large-scale production of human brain L-glutamate decarboxylase [J].
Davis, KM ;
Foos, T ;
Bates, CS ;
Tucker, E ;
Hsu, CC ;
Chen, WQ ;
Jin, H ;
Tyburski, JB ;
Schloss, JV ;
Tobin, AJ ;
Wu, JY .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 267 (03) :777-782
[9]   TARGETING OF THE 67-KDA ISOFORM OF GLUTAMIC-ACID DECARBOXYLASE TO INTRACELLULAR ORGANELLES IS MEDIATED BY ITS INTERACTION WITH THE NH2-TERMINAL REGION OF THE 65-KDA ISOFORM OF GLUTAMIC-ACID DECARBOXYLASE [J].
DIRKX, R ;
THOMAS, A ;
LI, LS ;
LERNMARK, A ;
SHERWIN, RS ;
DECAMILLI, P ;
SOLIMENA, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (05) :2241-2246
[10]   THE STRUCTURAL AND FUNCTIONAL-HETEROGENEITY OF GLUTAMIC-ACID DECARBOXYLASE - A REVIEW [J].
ERLANDER, MG ;
TOBIN, AJ .
NEUROCHEMICAL RESEARCH, 1991, 16 (03) :215-226