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J Cell Mol Med. 2015 Aug;19(8):1986-93. doi: 10.1111/jcmm.12580. Epub 2015 Apr 3.

Notch receptor expression in human brain arteriovenous malformations.

Author information

1
Department of Neurosurgery, Weis Center for Research, Geisinger Health System, Danville, PA, USA.
2
Laboratory Medicine, Geisinger Health System, Danville, PA, USA.
3
Department of Neurosurgery, Geisinger Health System, Danville, PA, USA.

Abstract

The roles of the Notch pathway proteins in normal adult vascular physiology and the pathogenesis of brain arteriovenous malformations are not well-understood. Notch 1 and 4 have been detected in human and mutant mice vascular malformations respectively. Although mutations in the human Notch 3 gene caused a genetic form of vascular stroke and dementia, its role in arteriovenous malformations development has been unknown. In this study, we performed immunohistochemistry screening on tissue microarrays containing eight surgically resected human brain arteriovenous malformations and 10 control surgical epilepsy samples. The tissue microarrays were evaluated for Notch 1-4 expression. We have found that compared to normal brain vascular tissue Notch-3 was dramatically increased in brain arteriovenous malformations. Similarly, Notch 4 labelling was also increased in vascular malformations and was confirmed by western blot analysis. Notch 2 was not detectable in any of the human vessels analysed. Using both immunohistochemistry on microarrays and western blot analysis, we have found that Notch-1 expression was detectable in control vessels, and discovered a significant decrease of Notch 1 expression in vascular malformations. We have demonstrated that Notch 3 and 4, and not Notch 1, were highly increased in human arteriovenous malformations. Our findings suggested that Notch 4, and more importantly, Notch 3, may play a role in the development and pathobiology of human arteriovenous malformations.

KEYWORDS:

BAVMs; cell signalling; endothelial cells; vascular malformations

PMID:
25846406
PMCID:
PMC4549049
DOI:
10.1111/jcmm.12580
[Indexed for MEDLINE]
Free PMC Article

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