Alterations of NURR1 and Cytokines in the Peripheral Blood Mononuclear Cells: Combined Biomarkers for Parkinson's Disease

Nuclear receptor related 1 protein ( ), a transcription factor as key player for maintaining dopamine neuron functions and regulating neuroinflammation in the central nerves system, is a potential susceptibility gene for Parkinson's disease (PD). To ascertain whether the expression levels of ge...

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Veröffentlicht in:Frontiers in aging neuroscience 2018-11, Vol.10, p.392-392
Hauptverfasser: Li, Tianbai, Yang, Zhaofei, Li, Song, Cheng, Cheng, Shen, Bairong, Le, Weidong
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Sprache:eng
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Zusammenfassung:Nuclear receptor related 1 protein ( ), a transcription factor as key player for maintaining dopamine neuron functions and regulating neuroinflammation in the central nerves system, is a potential susceptibility gene for Parkinson's disease (PD). To ascertain whether the expression levels of gene and inflammatory cytokines are altered in patients with PD, we measured their mRNA levels in the peripheral blood mononuclear cells (PBMCs) in 312 PD patients, 318 healthy controls (HC), and 332 non-PD neurological disease controls (NDCs) by quantitative real-time PCR. Our data showed that gene expression was significantly decreased in the PBMCs of PD as compared with that of HC and NDC ( < 0.01). Since was reported to have regulating effects on neuroinflammation, we assessed the expression levels of cytokines ( -α, β, , , and ) in the PBMCs of PD and controls (HC and NDC). Our results showed that the expression levels of those cytokines were significantly higher than those of controls. Statistical analysis revealed that expression presented a negative correlation with the expression of -α, β, , and , and collectively the measurements of plus those cytokines significantly improve the diagnostic accuracy. All these findings suggested that is likely to be involved in the process of PD by mediating the neuroinflammation, and the combination of and cytokines assessment in the PBMCs can be potential biomarkers for PD diagnosis.
ISSN:1663-4365
1663-4365
DOI:10.3389/fnagi.2018.00392