Genomic profiles for human peripheral blood T cells, B cells, natural killer cells, monocytes, and polymorphonuclear cells: Comparisons to ischemic stroke, migraine, and Tourette syndrome
被引:72
作者:
Du, XinLi
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机构:Univ Calif Davis, MIND Inst, Sacramento, CA 95817 USA
Du, XinLi
Tang, Yang
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机构:Univ Calif Davis, MIND Inst, Sacramento, CA 95817 USA
Tang, Yang
Xu, Huichun
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机构:Univ Calif Davis, MIND Inst, Sacramento, CA 95817 USA
Xu, Huichun
Lit, Lisa
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机构:Univ Calif Davis, MIND Inst, Sacramento, CA 95817 USA
Lit, Lisa
Walker, Wynn
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机构:Univ Calif Davis, MIND Inst, Sacramento, CA 95817 USA
Walker, Wynn
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机构:
Ashwood, Paul
Gregg, Jeffrey P.
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机构:Univ Calif Davis, MIND Inst, Sacramento, CA 95817 USA
Gregg, Jeffrey P.
Sharp, Frank R.
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机构:Univ Calif Davis, MIND Inst, Sacramento, CA 95817 USA
Sharp, Frank R.
机构:
[1] Univ Calif Davis, MIND Inst, Sacramento, CA 95817 USA
[2] Univ Calif Davis, Dept Neurol, Sacramento, CA 95817 USA
[3] Univ Calif Davis, Dept Pathol, Sacramento, CA 95817 USA
[4] Univ Calif Davis, Dept Med, Sacramento, CA 95817 USA
blood;
humans;
gene expression;
microarrays;
genome;
T cells;
B cells;
NK cells;
neutrophils;
migraine;
stroke;
Tourette;
D O I:
10.1016/j.ygeno.2006.02.003
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
Blood genomic profiling has been applied to disorders of the blood and various organ systems including brain to elucidate disease mechanisms and identify surrogate disease markers. Since most studies have not examined specific cell types, we performed a preliminary genomic survey of major blood cell types from normal individuals using microarrays. CD4(+) T cells, CD8(+) T cells, CD19(+) B cells, CD56(+) natural killer cells, and CD14(+) monocytes were negatively selected using the RosetteSep antibody cocktail, while polymorphonuclear leukocytes were separated with density gradient media. Genes differentially expressed by each cell type were identified. To demonstrate the potential use of such cell subtype-specific genomic expression data, a number of the major genes previously reported to be regulated in ischemic stroke, migraine, and Tourette syndrome are shown to be associated with distinct cell populations in blood. These specific gene expression, cell-type-related profiles will need to be confirmed in larger data sets and could be used to study these and many other neurological diseases. (c) 2006 Elsevier Inc. All rights reserved.