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Stemness-Associated Markers Are Expressed in Extracranial Arteriovenous Malformation

Objectives: Arteriovenous malformation (AVM) consists of a nidus with poorly formed low-resistance vessels in place of a functional capillary network. The role of somatic mutations in embryonic stem cells (ESCs) and vascular anomalies and the presence of primitive populations in vascular anomalies l...

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Autores principales: Luke Krishnan, Claire S., Brasch, Helen D., Patel, Josie, Bockett, Nicholas, Paterson, Erin, Davis, Paul F., Tan, Swee T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8017302/
https://www.ncbi.nlm.nih.gov/pubmed/33816543
http://dx.doi.org/10.3389/fsurg.2021.621089
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author Luke Krishnan, Claire S.
Brasch, Helen D.
Patel, Josie
Bockett, Nicholas
Paterson, Erin
Davis, Paul F.
Tan, Swee T.
author_facet Luke Krishnan, Claire S.
Brasch, Helen D.
Patel, Josie
Bockett, Nicholas
Paterson, Erin
Davis, Paul F.
Tan, Swee T.
author_sort Luke Krishnan, Claire S.
collection PubMed
description Objectives: Arteriovenous malformation (AVM) consists of a nidus with poorly formed low-resistance vessels in place of a functional capillary network. The role of somatic mutations in embryonic stem cells (ESCs) and vascular anomalies and the presence of primitive populations in vascular anomalies led us to investigate the presence of a primitive population in extracranial AVM. Methods: Extracranial AVM tissue samples from 12 patients were stained for stemness-associated markers OCT4, SOX2, NANOG, KLF4, and c-MYC using immunohistochemical staining. In situ hybridization (ISH) was performed on six tissue samples to determine transcript expression. Western blotting and RT-qPCR were performed on two AVM-derived primary cell lines to determine protein and transcript expression of these markers, respectively. Immunofluorescence staining was performed on two tissue samples to investigate marker co-localization. Results: Immunohistochemical staining demonstrated the expression of OCT4, SOX2, KLF4, and c-MYC on the endothelium and media of lesional vessels and cells within the stroma of the nidus in all 12 AVM tissue samples. ISH and RT-qPCR confirmed transcript expression of all five markers. Western blotting showed protein expression of all markers except NANOG. Immunofluorescence staining demonstrated an OCT4+/SOX2+/KLF4+/c-MYC+ population within the endothelium and media of the lesional vessels and cells within the stroma of the AVM nidus. Conclusions: Our findings may suggest the presence of a primitive population within the AVM nidus. Further investigation may lead to novel therapeutic targeting of this population.
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spelling pubmed-80173022021-04-03 Stemness-Associated Markers Are Expressed in Extracranial Arteriovenous Malformation Luke Krishnan, Claire S. Brasch, Helen D. Patel, Josie Bockett, Nicholas Paterson, Erin Davis, Paul F. Tan, Swee T. Front Surg Surgery Objectives: Arteriovenous malformation (AVM) consists of a nidus with poorly formed low-resistance vessels in place of a functional capillary network. The role of somatic mutations in embryonic stem cells (ESCs) and vascular anomalies and the presence of primitive populations in vascular anomalies led us to investigate the presence of a primitive population in extracranial AVM. Methods: Extracranial AVM tissue samples from 12 patients were stained for stemness-associated markers OCT4, SOX2, NANOG, KLF4, and c-MYC using immunohistochemical staining. In situ hybridization (ISH) was performed on six tissue samples to determine transcript expression. Western blotting and RT-qPCR were performed on two AVM-derived primary cell lines to determine protein and transcript expression of these markers, respectively. Immunofluorescence staining was performed on two tissue samples to investigate marker co-localization. Results: Immunohistochemical staining demonstrated the expression of OCT4, SOX2, KLF4, and c-MYC on the endothelium and media of lesional vessels and cells within the stroma of the nidus in all 12 AVM tissue samples. ISH and RT-qPCR confirmed transcript expression of all five markers. Western blotting showed protein expression of all markers except NANOG. Immunofluorescence staining demonstrated an OCT4+/SOX2+/KLF4+/c-MYC+ population within the endothelium and media of the lesional vessels and cells within the stroma of the AVM nidus. Conclusions: Our findings may suggest the presence of a primitive population within the AVM nidus. Further investigation may lead to novel therapeutic targeting of this population. Frontiers Media S.A. 2021-03-19 /pmc/articles/PMC8017302/ /pubmed/33816543 http://dx.doi.org/10.3389/fsurg.2021.621089 Text en Copyright © 2021 Luke Krishnan, Brasch, Patel, Bockett, Paterson, Davis and Tan. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). 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 Surgery
Luke Krishnan, Claire S.
Brasch, Helen D.
Patel, Josie
Bockett, Nicholas
Paterson, Erin
Davis, Paul F.
Tan, Swee T.
Stemness-Associated Markers Are Expressed in Extracranial Arteriovenous Malformation
title Stemness-Associated Markers Are Expressed in Extracranial Arteriovenous Malformation
title_full Stemness-Associated Markers Are Expressed in Extracranial Arteriovenous Malformation
title_fullStr Stemness-Associated Markers Are Expressed in Extracranial Arteriovenous Malformation
title_full_unstemmed Stemness-Associated Markers Are Expressed in Extracranial Arteriovenous Malformation
title_short Stemness-Associated Markers Are Expressed in Extracranial Arteriovenous Malformation
title_sort stemness-associated markers are expressed in extracranial arteriovenous malformation
topic Surgery
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8017302/
https://www.ncbi.nlm.nih.gov/pubmed/33816543
http://dx.doi.org/10.3389/fsurg.2021.621089
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