GABA-shunt enzymes activity in GH3 cells with reduced level of PMCA2 or PMCA3 isoform

被引:8
作者
Kowalski, Antoni [1 ]
Zylinska, Ludmila [1 ]
Boczek, Tomasz [1 ]
Rebas, Elzbieta [1 ]
机构
[1] Med Univ Lodz, Dept Mol Neurochem, PL-92215 Lodz, Poland
关键词
GABA; Glutamate decarboxylase; gamma-Aminobutyrate aminotransferase; Succinate semialdehyde dehydrogenase; GH3 cell line; Plasma membrane calcium ATPase; GLUTAMIC-ACID DECARBOXYLASE; SUCCINIC SEMIALDEHYDE DEHYDROGENASE; MESSENGER-RNA EXPRESSION; GAMMA-AMINOBUTYRIC-ACID; CRYSTAL-STRUCTURE; PC12; CELLS; BRAIN; DEFICIENCY; RECEPTORS; CALCIUM;
D O I
10.1016/j.bbrc.2011.07.043
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
GABA (gamma-aminobutyric acid) is important neurotransmitter and regulator of endocrine functions. Its metabolism involves three enzymes: glutamate decarboxylase (GAD65 and GAD67). GABA aminotransferase (GABA-T) and succinic semialdehyde dehydrogenase (SSADH). As many cellular processes GABA turnover can depend on calcium homeostasis, which is maintained by plasma membrane calcium ATPases (PMCAs). In excitable cells PMCA2 and PMCA3 isoforms are particularly important. In this study we focused on GABA-metabolizing enzymes expression and activity in rat anterior pituitary GH3 cells with suppressed expression of PMCA2 or PMCA3. We observed that PMCA3-reduced cells have increased GAD65 expression. Suppression of PMCA2 caused a decrease in total GAD and GABA-T activity. These results indicate that PMCA2 and PMCA3 presence may be an important regulatory factor in GABA metabolism. Results suggest that PMCA2 and PMCA3 function is rather related to regulation of GABA synthesis and degradation than supplying cells with metabolites, which can be potentially energetic source. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:815 / 820
页数:6
相关论文
共 30 条
[1]
Kinetic differences between the isoforms of glutamate decarboxylase: implications for the regulation of GABA synthesis [J].
Battaglioli, G ;
Liu, HC ;
Martin, DL .
JOURNAL OF NEUROCHEMISTRY, 2003, 86 (04) :879-887
[2]
Bowers G, 1998, J NEUROSCI, V18, P5938
[3]
A novel mechanism for GABA synthesis and packaging into synaptic vesicles [J].
Buddhala, Chandana ;
Hsu, Che-Chang ;
Wu, Jang-Yen .
NEUROCHEMISTRY INTERNATIONAL, 2009, 55 (1-3) :9-12
[4]
Succinic semialdehyde dehydrogenase deficiency:: GABAB receptor-mediated function [J].
Buzzi, Andrea ;
Wu, Ying ;
Frantseva, Marina V. ;
Velazquez, Jose L. Perez ;
Cortez, Miguel A. ;
Liu, Chun C. ;
Shen, Li Q. ;
Gibson, K. Michael ;
Snead, O. Carter, III .
BRAIN RESEARCH, 2006, 1090 :15-22
[5]
DEBOER T, 1977, J NEUROCHEM, V28, P471
[6]
Paracrinicity: The story of 30 years of cellular pituitary crosstalk [J].
Denef, C. .
JOURNAL OF NEUROENDOCRINOLOGY, 2008, 20 (01) :1-70
[7]
Dingledine R, 1999, PHARMACOL REV, V51, P7
[8]
Molecular and physiological evidence for functional γ-aminobutyric acid (GABA)-C receptors in growth hormone-secreting cells [J].
Gamel-Didelon, K ;
Kunz, L ;
Föhr, KJ ;
Gratzl, M ;
Mayerhofer, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (22) :20192-20195
[9]
Plasma membrane calcium ATPase plays a role in reducing Ca2+-mediated cytotoxicity in PC12 cells [J].
Garcia, ML ;
Usachev, YM ;
Thayer, SA ;
Strehler, EE ;
Windebank, AJ .
JOURNAL OF NEUROSCIENCE RESEARCH, 2001, 64 (06) :661-669
[10]
DISTRIBUTION OF SOME ENZYMES ASSOCIATED WITH METABOLISM OF GLUTAMATE ASPARTATE GAMMA-AMINOBUTYRATE AND GLUTAMINE IN CAT SPINAL CORD [J].
GRAHAM, LT ;
APRISON, MH .
JOURNAL OF NEUROCHEMISTRY, 1969, 16 (04) :559-&