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Status |
Public on Sep 25, 2017 |
Title |
Thrombospondin1 replacement prevents cerebral cavernos malformations |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
We have purified primary brain microvascular endothelial cells (BMEC) from mice bearing floxed alleles of Krit1 (Krit1fl/fl) and an endothelial specific tamoxifen-regulated Cre recombinase (Pdgfb-iCreERT2), and used these to delete Krit1 in a time-controlled manner (Krit1ECKO). To elucidate the pathogenesis of cerebral cavernous malformations (CCM) we used genome-wide RNA sequencing (RNA-seq) to characterize the transcriptome of primary BMEC following acute genetic inactivation of Krit1.
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Overall design |
Treatment of Krit1f/f-Pdgfb-iCreERT2 BMEC with 5 µM-hydroxy-tamoxifen deleted Krit1 (Krit1ECKO) reduced KRIT1 mRNA and protein by >90% within 5 days compared to hydroxy-tamoxifen-treated Krit1fl/fl controls. Three independent biological replicates were used for the analysis.
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Contributor(s) |
Lopez-Ramirez MA, Fonseca G, Ginsberg MH |
Citation(s) |
28970240 |
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Submission date |
Aug 15, 2016 |
Last update date |
May 15, 2019 |
Contact name |
Miguel Alejandro Lopez-Ramirez |
E-mail(s) |
malopezramirez@ucsd.edu
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Phone |
858-822-6487
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Organization name |
University of California, San Diego
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Department |
School of Medicine
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Street address |
9500 Gilman Drive
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City |
La Jolla |
State/province |
California/San Diego |
ZIP/Postal code |
92093 |
Country |
USA |
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Platforms (1) |
GPL17021 |
Illumina HiSeq 2500 (Mus musculus) |
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Samples (6)
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Relations |
BioProject |
PRJNA339007 |
SRA |
SRP082179 |