Specific AHNAK expression in brain endothelial cells with barrier properties
- PMID: 15493012
- DOI: 10.1002/jcp.20232
Specific AHNAK expression in brain endothelial cells with barrier properties
Abstract
The blood-brain barrier (BBB) is essential for maintaining brain homeostasis and low permeability. Because disruption of the BBB may contribute to many brain disorders, they are of considerable interests in the identification of the molecular mechanisms of BBB development and integrity. We here report that the giant protein AHNAK is expressed at the plasma membrane of endothelial cells (ECs) forming specific blood-tissue barriers, but is absent from the endothelium of capillaries characterized by extensive molecular exchanges between blood and extracellular fluid. In the brain, AHNAK is widely distributed in ECs with BBB properties, where it co-localizes with the tight junction protein ZO-1. AHNAK is absent from the permeable brain ECs of the choroid plexus and is down-regulated in permeable angiogenic ECs of brain tumors. In the choroid plexus, AHNAK accumulates at the tight junctions of the choroid epithelial cells that form the blood-cerebrospinal fluid (CSF) barrier. In EC cultures, the regulation of AHNAK expression and its localization corresponds to general criteria of a protein involved in barrier organization. AHNAK is up-regulated by angiopoietin-1 (Ang-1), a morphogenic factor that regulates brain EC permeability. In bovine cerebral ECs co-cultured with glial cells, AHNAK relocates from the cytosol to the plasma membrane when endothelial cells acquire BBB properties. Our results identify AHNAK as a protein marker of endothelial cells with barrier properties.
Copyright 2004 Wiley-Liss, Inc.
Similar articles
-
Induction of blood-brain barrier properties in cultured brain capillary endothelial cells: comparison between primary glial cells and C6 cell line.Glia. 2005 Aug 15;51(3):187-98. doi: 10.1002/glia.20189. Glia. 2005. PMID: 15800928
-
A new blood-brain barrier model using primary rat brain endothelial cells, pericytes and astrocytes.Neurochem Int. 2009 Mar-Apr;54(3-4):253-63. doi: 10.1016/j.neuint.2008.12.002. Epub 2008 Dec 7. Neurochem Int. 2009. PMID: 19111869
-
Closing the gap between the in-vivo and in-vitro blood-brain barrier tightness.Brain Res. 2009 Aug 11;1284:12-21. doi: 10.1016/j.brainres.2009.05.072. Epub 2009 Jun 6. Brain Res. 2009. PMID: 19501061
-
Brain iron homeostasis.Dan Med Bull. 2002 Nov;49(4):279-301. Dan Med Bull. 2002. PMID: 12553165 Review.
-
[The blood-brain barrier. II. Physiological data].Rev Neurol (Paris). 1984;140(1):3-13. Rev Neurol (Paris). 1984. PMID: 6364292 Review. French.
Cited by
-
AHNAKs roles in physiology and malignant tumors.Front Oncol. 2023 Nov 14;13:1258951. doi: 10.3389/fonc.2023.1258951. eCollection 2023. Front Oncol. 2023. PMID: 38033502 Free PMC article. Review.
-
Valosin-containing protein (VCP), a component of tumor-derived extracellular vesicles, impairs the barrier integrity of brain microvascular endothelial cells.BBA Adv. 2024 Dec 12;7:100130. doi: 10.1016/j.bbadva.2024.100130. eCollection 2025. BBA Adv. 2024. PMID: 39802400 Free PMC article.
-
Profiling the proteomic inflammatory state of human astrocytes using DIA mass spectrometry.J Neuroinflammation. 2018 Nov 30;15(1):331. doi: 10.1186/s12974-018-1371-6. J Neuroinflammation. 2018. PMID: 30501627 Free PMC article.
-
MAP3K4 Controls the Chromatin Modifier HDAC6 during Trophoblast Stem Cell Epithelial-to-Mesenchymal Transition.Cell Rep. 2017 Mar 7;18(10):2387-2400. doi: 10.1016/j.celrep.2017.02.030. Cell Rep. 2017. PMID: 28273454 Free PMC article.
-
Identification of pannexin 1-regulated genes, interactome, and pathways in rhabdomyosarcoma and its tumor inhibitory interaction with AHNAK.Oncogene. 2021 Mar;40(10):1868-1883. doi: 10.1038/s41388-020-01623-2. Epub 2021 Feb 9. Oncogene. 2021. PMID: 33564071 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous