A monocyte gene expression signature in the early clinical course of Parkinson's disease

被引:41
作者
Schlachetzki, Johannes C. M. [1 ,2 ]
Prots, Iryna [3 ]
Tao, Jenhan [2 ]
Chun, Hyun B. [2 ]
Saijo, Kaoru [4 ]
Gosselin, David [2 ,5 ]
Winner, Beate [3 ]
Glass, Christopher K. [2 ]
Winkler, Juergen [1 ]
机构
[1] Friedrich Alexander Univ FAU Erlangen Nurnberg, Univ Hosp Erlangen, Dept Mol Neurol, D-91054 Erlangen, Germany
[2] Univ Calif San Diego, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
[3] FAU Erlangen Nurnberg, Dept Stem Cell Biol, D-91054 Erlangen, Germany
[4] Univ Calif Berkeley, Helen Wills Neurosci Inst, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[5] Univ Laval, CHU Quebec, Ctr Rech, Dept Mol Med, Quebec City, PQ G1V 4G2, Canada
关键词
ALPHA-SYNUCLEIN; MYELOID CELLS; BLOOD MONOCYTES; RISK LOCI; RNA-SEQ; MICROGLIA; REVEALS; MACROPHAGES; HETEROGENEITY; VARIABILITY;
D O I
10.1038/s41598-018-28986-7
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
Microglia are the main immune cells of the brain and express a large genetic pattern of genes linked to Parkinson's disease risk alleles. Monocytes like microglia are myeloid-lineage cells, raising the questions of the extent to which they share gene expression with microglia and whether they are already altered early in the clinical course of the disease. To decipher a monocytic gene expression signature in Parkinson's disease, we performed RNA-seq and applied the two-sample Kolmogorov-Smirnov test to identify differentially expressed genes between controls and patients with Parkinson's disease and changes in gene expression variability and dysregulation. The gene expression profiles of normal human monocytes and microglia showed a plethora of differentially expressed genes. Additionally, we identified a distinct gene expression pattern of monocytes isolated from Parkinson's disease patients at an early disease stage compared to controls using the Kolmogorov-Smirnov test. Differentially expressed genes included genes involved in immune activation such as HLA-DQB1, MYD88, REL, and TNF-alpha. Our data suggest that future studies of distinct leukocyte subsets are warranted to identify possible surrogate biomarkers and may lead to the identification of novel interventions early in the disease course.
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页数:13
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