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Status |
Public on Jun 11, 2014 |
Title |
Linking Notch signaling to ischemic stroke |
Organism |
Mus musculus |
Experiment type |
Expression profiling by array
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Summary |
Using a hitherto uncharacterized knockout mouse model of Notch 3, a Notch signaling receptor paralogue highly expressed in vascular SMCs, we uncover a striking susceptibility to ischemic stroke upon challenge. Cellular and molecular analyses of vascular SMCs derived from these animals associate Notch 3 activity to the expression of specific gene targets, whereas genetic rescue experiments unambiguously link Notch 3 function in vessels to the ischemic phenotype.
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Overall design |
Microarray Studies. Biotinylated cRNA samples from freshly sorted brain SMCs (four Notch 3 +/− mice and five Notch 3 −/− mice) were fragmented before hybridization (15 μg each) onto mouse 430 2.0 Affymetrix chips. The chips were washed, stained by using strepavidin-phycoerytrin, and scanned the next day as described in ref. 24. For data normalization, all probe sets were scaled to a target intensity of 150. Microarray data analysis was performed by using Rosetta Resolver. All cells were from 10- to 12-week-old male mice. Gene Ontology Analyses. PANTHER software was used to define over- and underrepresented functions in the list of signature genes found by microarray analysis (25). P values were calculated by using binomial statistics.
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Contributor(s) |
Arboleda-Velasquez J, Artavanis-Tsakonas S |
Citation(s) |
25015359 |
Submission date |
Jun 10, 2014 |
Last update date |
Feb 11, 2019 |
Contact name |
Joseph Arboleda-Velasquez |
E-mail(s) |
vincent_primo@meei.harvard.edu
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Phone |
6179122558
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Organization name |
Schepens Eye Research Institute
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Department |
Opthalmology
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Lab |
D'Amore lab
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Street address |
20 Staniford st
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City |
Boston |
State/province |
MA |
ZIP/Postal code |
01906 |
Country |
USA |
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Platforms (1) |
GPL1261 |
[Mouse430_2] Affymetrix Mouse Genome 430 2.0 Array |
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Samples (15)
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Relations |
BioProject |
PRJNA252379 |