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Single-cell RNA sequencing provides novel insights to pathologic pathways in abdominal aortic aneurysm

There is gaining popularity in the use of single-cell technology and analysis in studying the pathogenesis of abdominal aortic aneurysm (AAA). As there are no current pharmacologic therapies for impeding aneurysm growth or preventing AAA rupture, identifying key pathways involved in AAA formation is...

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Detalles Bibliográficos
Autores principales: Bontekoe, Jack, Liu, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241995/
https://www.ncbi.nlm.nih.gov/pubmed/37288252
http://dx.doi.org/10.3389/fcvm.2023.1172080
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author Bontekoe, Jack
Liu, Bo
author_facet Bontekoe, Jack
Liu, Bo
author_sort Bontekoe, Jack
collection PubMed
description There is gaining popularity in the use of single-cell technology and analysis in studying the pathogenesis of abdominal aortic aneurysm (AAA). As there are no current pharmacologic therapies for impeding aneurysm growth or preventing AAA rupture, identifying key pathways involved in AAA formation is critical for the development of future therapies. Single-cell RNA sequencing (scRNA-seq) technology provides an unbiased and global view of transcriptomic characteristics within each of the major cell types in aneurysmal tissues. In this brief review, we examine the current literature utilizing scRNA-seq for the analysis of AAA and discuss trends and future utility of this technology.
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spelling pubmed-102419952023-06-07 Single-cell RNA sequencing provides novel insights to pathologic pathways in abdominal aortic aneurysm Bontekoe, Jack Liu, Bo Front Cardiovasc Med Cardiovascular Medicine There is gaining popularity in the use of single-cell technology and analysis in studying the pathogenesis of abdominal aortic aneurysm (AAA). As there are no current pharmacologic therapies for impeding aneurysm growth or preventing AAA rupture, identifying key pathways involved in AAA formation is critical for the development of future therapies. Single-cell RNA sequencing (scRNA-seq) technology provides an unbiased and global view of transcriptomic characteristics within each of the major cell types in aneurysmal tissues. In this brief review, we examine the current literature utilizing scRNA-seq for the analysis of AAA and discuss trends and future utility of this technology. Frontiers Media S.A. 2023-05-23 /pmc/articles/PMC10241995/ /pubmed/37288252 http://dx.doi.org/10.3389/fcvm.2023.1172080 Text en © 2023 Bontekoe and Liu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cardiovascular Medicine
Bontekoe, Jack
Liu, Bo
Single-cell RNA sequencing provides novel insights to pathologic pathways in abdominal aortic aneurysm
title Single-cell RNA sequencing provides novel insights to pathologic pathways in abdominal aortic aneurysm
title_full Single-cell RNA sequencing provides novel insights to pathologic pathways in abdominal aortic aneurysm
title_fullStr Single-cell RNA sequencing provides novel insights to pathologic pathways in abdominal aortic aneurysm
title_full_unstemmed Single-cell RNA sequencing provides novel insights to pathologic pathways in abdominal aortic aneurysm
title_short Single-cell RNA sequencing provides novel insights to pathologic pathways in abdominal aortic aneurysm
title_sort single-cell rna sequencing provides novel insights to pathologic pathways in abdominal aortic aneurysm
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241995/
https://www.ncbi.nlm.nih.gov/pubmed/37288252
http://dx.doi.org/10.3389/fcvm.2023.1172080
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