Comparative transcriptomics of choroid plexus in Alzheimer's disease, frontotemporal dementia and Huntington's disease: implications for CSF homeostasis

Autor: Stopa, Edward G, Tanis, Keith Q, Miller, Miles C, Nikonova, Elena V, Podtelezhnikov, Alexei A, Finney, Eva M, Stone, David J, Camargo, Luiz M, Parker, Lisan, Verma, Ajay, Baird, Andrew, Donahue, John E, Torabi, Tara, Eliceiri, Brian P, Silverberg, Gerald D, Johanson, Conrad E
Rok vydání: 2018
Předmět:
Adult
Male
Cadherin-mediated adhesion
Aging
CSF homocysteine
LRP-1
Gene Expression
Peroxisome-proliferator-activated receptor (PPAR)
Peroxisome-proliferator-activated receptor
Neurodegenerative
Alzheimer's Disease
Medical and Health Sciences
Janus kinase/signal transducers and activators of transcription (JAK-STAT)
Rare Diseases
Alzheimer Disease
80 and over
Acquired Cognitive Impairment
Genetics
Humans
Homeostasis
Mechanistic target of rapamycin (mTOR)
Choroid plexus transcriptome
Aged
Neurosciences
Blood-CSF barrier inflammatome
Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD)
Middle Aged
Neuroimmune CSF regulation
Biological Sciences
Microarray Analysis
Blood–CSF barrier inflammatome
Brain Disorders
Huntington Disease
Frontotemporal Dementia
Choroid Plexus
Neurological
Female
Dementia
Janus kinase/signal transducers and activators of transcription
Vascular endothelial growth factor
Transcriptome
Mechanistic target of rapamycin
Choroid plexus methionine
Zdroj: Fluids and barriers of the CNS, vol 15, iss 1
Stopa, EG; Tanis, KQ; Miller, MC; Nikonova, EV; Podtelezhnikov, AA; Finney, EM; et al.(2018). Comparative transcriptomics of choroid plexus in Alzheimer's disease, frontotemporal dementia and Huntington's disease: implications for CSF homeostasis. FLUIDS AND BARRIERS OF THE CNS, 15. doi: 10.1186/s12987-018-0102-9. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/4tn4j1xw
DOI: 10.1186/s12987-018-0102-9.
Popis: BACKGROUND:In Alzheimer's disease, there are striking changes in CSF composition that relate to altered choroid plexus (CP) function. Studying CP tissue gene expression at the blood-cerebrospinal fluid barrier could provide further insight into the epithelial and stromal responses to neurodegenerative disease states. METHODS:Transcriptome-wide Affymetrix microarrays were used to determine disease-related changes in gene expression in human CP. RNA from post-mortem samples of the entire lateral ventricular choroid plexus was extracted from 6 healthy controls (Ctrl), 7 patients with advanced (Braak and Braak stage III-VI) Alzheimer's disease (AD), 4 with frontotemporal dementia (FTD) and 3 with Huntington's disease (HuD). Statistics and agglomerative clustering were accomplished with MathWorks, MatLab; and gene set annotations by comparing input sets to GeneGo ( http://www.genego.com ) and Ingenuity ( http://www.ingenuity.com ) pathway sets. Bonferroni-corrected hypergeometric p-values of
Databáze: OpenAIRE