Identification of nigral dopaminergic neuron-enriched genes in adult rats

被引:40
作者
Zhou, Qinbo [1 ,2 ]
Li, Juntao [1 ]
Wang, Hanzhi [1 ,2 ]
Yin, Yanqing [1 ]
Zhou, Jiawei [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Biol Sci, State Key Lab Neurobiol, Inst Neurosci, Shanghai 200031, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Biol Sci, Inst Biochem & Cell Biol, Mol Cell Biol Lab, Shanghai 200031, Peoples R China
关键词
Substantia nigra; Dopaminergic neurons; Microarray; Affymetrix; Gene expression; DIFFERENTIAL EXPRESSION; HEMIPARKINSONIAN RATS; PARKINSONS-DISEASE; SUBSTANTIA-NIGRA; GDNF-FAMILY; IN-VITRO; DEGENERATION; PROTEIN; 6-HYDROXYDOPAMINE; VULNERABILITY;
D O I
10.1016/j.neurobiolaging.2009.02.009
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Dopaminergic (DA) neurons in the substantia nigra play crucial roles in movement control and other physiological activities. Degeneration of these neurons is closely associated with Parkinson's disease. However, the molecular identity of nigral DA neurons is not fully understood. To identify nigral DA neuron-enriched genes, we used microarrays to compare the genome-wide gene expression profiles in 6-hydroxydopamine-lesioned, and control, substantia nigra. We identified a total of 88 unique differentially expressed gene transcripts. The spatial expression patterns of a set of these genes, including Slc10a4, Rit2, F2r, Snx10 and Slc24a3, were validated by in situ hybridization. It was revealed that their expression was highly specific in the substantia nigra. Thus we identified a set of genes that are highly expressed in nigral DA neurons, and may be involved in the maintenance and survival of nigral DA neurons in the adult rat brain. Our study also provides a general approach for profiling cell type-specific gene expression in the mature mammalian brain. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:313 / 326
页数:14
相关论文
共 33 条
[1]   The GDNF family: Signalling, biological functions and therapeutic value [J].
Airaksinen, MS ;
Saarma, M .
NATURE REVIEWS NEUROSCIENCE, 2002, 3 (05) :383-394
[2]   Gene Ontology: tool for the unification of biology [J].
Ashburner, M ;
Ball, CA ;
Blake, JA ;
Botstein, D ;
Butler, H ;
Cherry, JM ;
Davis, AP ;
Dolinski, K ;
Dwight, SS ;
Eppig, JT ;
Harris, MA ;
Hill, DP ;
Issel-Tarver, L ;
Kasarskis, A ;
Lewis, S ;
Matese, JC ;
Richardson, JE ;
Ringwald, M ;
Rubin, GM ;
Sherlock, G .
NATURE GENETICS, 2000, 25 (01) :25-29
[3]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[4]   Cell type-specific gene expression of midbrain dopaminergic neurons reveals molecules involved in their vulnerability and protection [J].
Chung, CY ;
Seo, H ;
Sonntag, KC ;
Brooks, A ;
Lin, L ;
Isacson, O .
HUMAN MOLECULAR GENETICS, 2005, 14 (13) :1709-1725
[5]   Molecular pathways of neurodegeneration in Parkinson's disease [J].
Dawson, TM ;
Dawson, VL .
SCIENCE, 2003, 302 (5646) :819-822
[6]   The solute carrier family SLC10: more than a family of bile acid transporters regarding function and phylogenetic relationships [J].
Geyer, J ;
Wilke, T ;
Petzinger, E .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 2006, 372 (06) :413-431
[7]   Differential expression of striatal synaptotagmin mRNA isoforms in hemiparkinsonian rats [J].
Glavan, G ;
Zivin, M .
NEUROSCIENCE, 2005, 135 (02) :545-554
[8]   Dopaminergic regulation of synaptotagmin I and IV mRNAs in hemiparkinsonian rats [J].
Glavan, G ;
Zorec, R ;
Babic, K ;
Sket, D ;
Zivin, M .
NEUROREPORT, 2000, 11 (18) :4043-4047
[9]   Gene expression profiles of brain dopamine neurons and relevance to neuropsychiatric disease [J].
Greene, James G. .
JOURNAL OF PHYSIOLOGY-LONDON, 2006, 575 (02) :411-416
[10]   Gene expression profiling of rat midbrain dopamine neurons: implications for selective vulnerability in parkinsonism [J].
Greene, JG ;
Dingledine, R ;
Greenamyre, JT .
NEUROBIOLOGY OF DISEASE, 2005, 18 (01) :19-31