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Hedgehog and Resident Vascular Stem Cell Fate

The Hedgehog pathway is a pivotal morphogenic driver during embryonic development and a key regulator of adult stem cell self-renewal. The discovery of resident multipotent vascular stem cells and adventitial progenitors within the vessel wall has transformed our understanding of the origin of media...

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Autores principales: Mooney, Ciaran J., Hakimjavadi, Roya, Fitzpatrick, Emma, Kennedy, Eimear, Walls, Dermot, Morrow, David, Redmond, Eileen M., Cahill, Paul A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4438189/
https://www.ncbi.nlm.nih.gov/pubmed/26064136
http://dx.doi.org/10.1155/2015/468428
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author Mooney, Ciaran J.
Hakimjavadi, Roya
Fitzpatrick, Emma
Kennedy, Eimear
Walls, Dermot
Morrow, David
Redmond, Eileen M.
Cahill, Paul A.
author_facet Mooney, Ciaran J.
Hakimjavadi, Roya
Fitzpatrick, Emma
Kennedy, Eimear
Walls, Dermot
Morrow, David
Redmond, Eileen M.
Cahill, Paul A.
author_sort Mooney, Ciaran J.
collection PubMed
description The Hedgehog pathway is a pivotal morphogenic driver during embryonic development and a key regulator of adult stem cell self-renewal. The discovery of resident multipotent vascular stem cells and adventitial progenitors within the vessel wall has transformed our understanding of the origin of medial and neointimal vascular smooth muscle cells (SMCs) during vessel repair in response to injury, lesion formation, and overall disease progression. This review highlights the importance of components of the Hh and Notch signalling pathways within the medial and adventitial regions of adult vessels, their recapitulation following vascular injury and disease progression, and their putative role in the maintenance and differentiation of resident vascular stem cells to vascular lineages from discrete niches within the vessel wall.
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spelling pubmed-44381892015-06-10 Hedgehog and Resident Vascular Stem Cell Fate Mooney, Ciaran J. Hakimjavadi, Roya Fitzpatrick, Emma Kennedy, Eimear Walls, Dermot Morrow, David Redmond, Eileen M. Cahill, Paul A. Stem Cells Int Review Article The Hedgehog pathway is a pivotal morphogenic driver during embryonic development and a key regulator of adult stem cell self-renewal. The discovery of resident multipotent vascular stem cells and adventitial progenitors within the vessel wall has transformed our understanding of the origin of medial and neointimal vascular smooth muscle cells (SMCs) during vessel repair in response to injury, lesion formation, and overall disease progression. This review highlights the importance of components of the Hh and Notch signalling pathways within the medial and adventitial regions of adult vessels, their recapitulation following vascular injury and disease progression, and their putative role in the maintenance and differentiation of resident vascular stem cells to vascular lineages from discrete niches within the vessel wall. Hindawi Publishing Corporation 2015 2015-05-06 /pmc/articles/PMC4438189/ /pubmed/26064136 http://dx.doi.org/10.1155/2015/468428 Text en Copyright © 2015 Ciaran J. Mooney et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Mooney, Ciaran J.
Hakimjavadi, Roya
Fitzpatrick, Emma
Kennedy, Eimear
Walls, Dermot
Morrow, David
Redmond, Eileen M.
Cahill, Paul A.
Hedgehog and Resident Vascular Stem Cell Fate
title Hedgehog and Resident Vascular Stem Cell Fate
title_full Hedgehog and Resident Vascular Stem Cell Fate
title_fullStr Hedgehog and Resident Vascular Stem Cell Fate
title_full_unstemmed Hedgehog and Resident Vascular Stem Cell Fate
title_short Hedgehog and Resident Vascular Stem Cell Fate
title_sort hedgehog and resident vascular stem cell fate
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4438189/
https://www.ncbi.nlm.nih.gov/pubmed/26064136
http://dx.doi.org/10.1155/2015/468428
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