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Expression of periaxin (PRX) specifically in the human cerebrovascular system: PDZ domain-mediated strengthening of endothelial barrier function
- Source :
- Scientific Reports, Scientific Reports, Vol 8, Iss 1, Pp 1-15 (2018)
- Publication Year :
- 2017
-
Abstract
- Regulation of cerebral endothelial cell function plays an essential role in changes in blood-brain barrier permeability. Proteins that are important for establishment of endothelial tight junctions have emerged as critical molecules, and PDZ domain containing-molecules are among the most important. We have discovered that the PDZ-domain containing protein periaxin (PRX) is expressed in human cerebral endothelial cells. Surprisingly, PRX protein is not detected in brain endothelium in other mammalian species, suggesting that it could confer human-specific vascular properties. In endothelial cells, PRX is predominantly localized to the nucleus and not tight junctions. Transcriptome analysis shows that PRX expression suppresses, by at least 50%, a panel of inflammatory markers, of which 70% are Type I interferon response genes; only four genes were significantly activated by PRX expression. When expressed in mouse endothelial cells, PRX strengthens barrier function, significantly increases transendothelial electrical resistance (~35%; p
- Subjects :
- 0301 basic medicine
Cell Membrane Permeability
Endothelium
PDZ domain
lcsh:Medicine
Gene Expression
PDZ Domains
Article
Cell Line
Tight Junctions
Transcriptome
03 medical and health sciences
Mice
Gene expression
medicine
Animals
Humans
lcsh:Science
Barrier function
Cell Nucleus
Multidisciplinary
Tight junction
Chemistry
lcsh:R
Brain
Endothelial Cells
Membrane Proteins
Cell biology
Endothelial stem cell
Mice, Inbred C57BL
030104 developmental biology
medicine.anatomical_structure
Cell culture
Blood-Brain Barrier
Cerebrovascular Circulation
lcsh:Q
Endothelium, Vascular
Subjects
Details
- ISSN :
- 20452322
- Volume :
- 8
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Scientific reports
- Accession number :
- edsair.doi.dedup.....4b95759145feecbf1cd0d902f8b4e496