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Microsurgical Venous Pouch Arterial-Bifurcation Aneurysms in the Rabbit Model: Technical Aspects
Published on: May 11, 2011
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RNA-Sequencing Analysis of Messenger RNA/MicroRNA in a Rabbit Aneurysm Model Identifies Pathways and Genes of
1From the Neuroradiology Research Laboratory, Mayo Clinic, Rochester, Minnesota.
AJNR. American Journal of Neuroradiology
|August 1, 2015
Summary
RNA sequencing of rabbit aneurysms identified key genes and microRNAs involved in inflammation and coagulation. This study highlights ANKRD1 and TACR1 as potential targets for matrix metalloproteinase regulation.
Area of Science:
- Vascular Biology
- Genomics
- Molecular Medicine
Background:
- Rabbit aneurysm models are crucial for studying intracranial aneurysms and testing embolization devices.
- Understanding the molecular mechanisms of aneurysm growth and healing is essential for clinical applications.
- RNA sequencing offers a powerful tool to explore gene expression in aneurysm biology.
Purpose of the Study:
- To identify genes and microRNAs relevant to induced rabbit aneurysm biology using RNA sequencing.
- To uncover genes and pathways of potential clinical significance in aneurysm development.
- To investigate the role of noncoding RNAs, specifically microRNAs, in aneurysm pathogenesis.
Main Methods:
- Saccular aneurysms were created in rabbits using elastase induction.
- Messenger RNA and microRNA were isolated from aneurysm and control carotid artery tissues at 12 weeks.
- RNA sequencing was performed, followed by Ingenuity Pathway Analysis for data interpretation.
Main Results:
- RNA sequencing analyzed 9396 genes, with 6.9% showing significant differential expression.
- 143 genes were down-regulated and 471 up-regulated in aneurysms compared to controls.
- 5 microRNAs were up-regulated and 3 down-regulated; pathway analysis linked genes to inflammation, migration, and coagulation.
Conclusions:
- RNA sequencing revealed differential regulation of inflammation and antigen presentation pathways in rabbit aneurysms.
- ANKRD1 and TACR1 were identified as significant genes involved in regulating matrix metalloproteinases.
- The findings provide insights into the molecular underpinnings of aneurysm biology and potential therapeutic targets.

