Dokumentdetails
ID

doi:10.1186/s12888-023-04634-x...

Autor
Huang, Jiewen Song, Zhen Wei, Beiwen Li, Qingtian Lin, Ping Li, Hui Dong, Ke
Langue
en
Editor

BioMed Central

Kategorie

Medicine & Public Health

Jahr

2023

Auflistungsdatum

15.03.2023

Schlüsselwörter
alzheimer's disease mitogen peripheral blood mononuclear cell pha lps cell-free levels secretion stimulated pbmcs alzheimer disease mitochondrial dna
Metrisch

Zusammenfassung

Background Based on its objective characteristics, laboratory markers have always been the research direction of clinical diagnosis and assessment of mental disorders including Alzheimer's disease.

Methods MTT Colorimetric Assay, ELISA, and quantitative PCR were used to investigate the responsiveness of peripheral blood mononuclear cells (PBMCs) to mitogen Lipopolysaccharides (LPS) and Phytohemagglutinin (PHA), PBMCs genomic methylation and hydroxymethylation levels, nuclear DNA and mitochondrial DNA damage, respiratory chain enzyme activities, and circulating cell-free mitochondrial DNA levels were detected in 90 patients with Alzheimer's disease.

Results In the Alzheimer's disease group, LPS stimulated PBMCs viability, TNF-α secretion, PHA stimulated IL-10 secretion, genomic DNA methylation levels, circulating cell-free mitochondrial DNA copies, citrate synthase activity were reduced compared to the control; while the LPS stimulated PBMCs IL-1α secretion, PHA stimulated IL-1α and IFN-γ secretion, plasma IL-6 and TNF-α, mitochondrial DNA damages were increased compared to the control.

Conclusions The reactivity of peripheral blood mononuclear cells to mitogens, mitochondrial DNA integrity characteristics, and cell-free mitochondrial DNA copies may be used as candidate laboratory biomarkers to help clinical management of Alzheimer's disease.

Huang, Jiewen,Song, Zhen,Wei, Beiwen,Li, Qingtian,Lin, Ping,Li, Hui,Dong, Ke, 2023, Immunological evaluation of patients with Alzheimer's disease based on mitogen-stimulated cytokine productions and mitochondrial DNA indicators, BioMed Central

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