Cargando…

Pericardial Patch Angioplasty Heals via an Ephrin-B2 and CD34 Positive Cell Mediated Mechanism

OBJECTIVE: Pericardial patches are commonly used in vascular surgery to close arteriotomies. The mechanism of early healing after patch implantation is still not well defined. We used a rat aortic patch model to assess pericardial patch healing and examined Ephrin-B2, a marker of arterial identity,...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Xin, Jadlowiec, Caroline, Guo, Yuanyuan, Protack, Clinton D., Ziegler, Kenneth R., Lv, Wei, Yang, Chenzi, Shu, Chang, Dardik, Alan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3374760/
https://www.ncbi.nlm.nih.gov/pubmed/22719962
http://dx.doi.org/10.1371/journal.pone.0038844
_version_ 1782235675304656896
author Li, Xin
Jadlowiec, Caroline
Guo, Yuanyuan
Protack, Clinton D.
Ziegler, Kenneth R.
Lv, Wei
Yang, Chenzi
Shu, Chang
Dardik, Alan
author_facet Li, Xin
Jadlowiec, Caroline
Guo, Yuanyuan
Protack, Clinton D.
Ziegler, Kenneth R.
Lv, Wei
Yang, Chenzi
Shu, Chang
Dardik, Alan
author_sort Li, Xin
collection PubMed
description OBJECTIVE: Pericardial patches are commonly used in vascular surgery to close arteriotomies. The mechanism of early healing after patch implantation is still not well defined. We used a rat aortic patch model to assess pericardial patch healing and examined Ephrin-B2, a marker of arterial identity, expression within the post-implantation patch. We also determined whether endothelial progenitor cells (EPC) are associated with early patch healing in the arterial environment. METHODS: Wistar rats (200–250 grams) underwent infrarenal aortic arteriotomy and then closure via bovine or porcine pericardial patch angioplasty. Control groups included subcutaneously implanted patches. Patches were harvested at 0–30 days and analyzed by histology, immunohistochemistry, immunofluorescence and Western blot as well as quantitative PCR. RESULTS: Prior to implantation, pericardial patches are largely composed of collagen and are acellular. Following arterial implantation, increasing numbers of CD68-positive cells as well as Ephrin-B2 and CD34 dual-positive cells are found within both bovine and porcine pericardial patches, whereas the infiltrating cells are negative for vWF and α-actin. Porcine patches have a luminal monolayer of cells at day 7, compared to bovine patches that have fewer luminal cells. Subcutaneously implanted patches do not attract Ephrin-B2/CD34-positive cells. By day 30, both bovine and porcine pericardial patches develop a neointima that contains Ephrin-B2, CD34, and VEGFR2-positive cells. CONCLUSION: Both CD68-positive and Ephrin-B2 and CD34 dual-positive cells infiltrate the pericardial patch early after implantation. Arteriotomy closure via pericardial patch angioplasty shows patch adaptation to the arterial environment that may involve a foreign body response as well as localization of EPC. Arterial remodeling of pericardial patches support endothelialization and may represent a paradigm of healing of scaffolds used for tissue engineering.
format Online
Article
Text
id pubmed-3374760
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-33747602012-06-20 Pericardial Patch Angioplasty Heals via an Ephrin-B2 and CD34 Positive Cell Mediated Mechanism Li, Xin Jadlowiec, Caroline Guo, Yuanyuan Protack, Clinton D. Ziegler, Kenneth R. Lv, Wei Yang, Chenzi Shu, Chang Dardik, Alan PLoS One Research Article OBJECTIVE: Pericardial patches are commonly used in vascular surgery to close arteriotomies. The mechanism of early healing after patch implantation is still not well defined. We used a rat aortic patch model to assess pericardial patch healing and examined Ephrin-B2, a marker of arterial identity, expression within the post-implantation patch. We also determined whether endothelial progenitor cells (EPC) are associated with early patch healing in the arterial environment. METHODS: Wistar rats (200–250 grams) underwent infrarenal aortic arteriotomy and then closure via bovine or porcine pericardial patch angioplasty. Control groups included subcutaneously implanted patches. Patches were harvested at 0–30 days and analyzed by histology, immunohistochemistry, immunofluorescence and Western blot as well as quantitative PCR. RESULTS: Prior to implantation, pericardial patches are largely composed of collagen and are acellular. Following arterial implantation, increasing numbers of CD68-positive cells as well as Ephrin-B2 and CD34 dual-positive cells are found within both bovine and porcine pericardial patches, whereas the infiltrating cells are negative for vWF and α-actin. Porcine patches have a luminal monolayer of cells at day 7, compared to bovine patches that have fewer luminal cells. Subcutaneously implanted patches do not attract Ephrin-B2/CD34-positive cells. By day 30, both bovine and porcine pericardial patches develop a neointima that contains Ephrin-B2, CD34, and VEGFR2-positive cells. CONCLUSION: Both CD68-positive and Ephrin-B2 and CD34 dual-positive cells infiltrate the pericardial patch early after implantation. Arteriotomy closure via pericardial patch angioplasty shows patch adaptation to the arterial environment that may involve a foreign body response as well as localization of EPC. Arterial remodeling of pericardial patches support endothelialization and may represent a paradigm of healing of scaffolds used for tissue engineering. Public Library of Science 2012-06-13 /pmc/articles/PMC3374760/ /pubmed/22719962 http://dx.doi.org/10.1371/journal.pone.0038844 Text en This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Li, Xin
Jadlowiec, Caroline
Guo, Yuanyuan
Protack, Clinton D.
Ziegler, Kenneth R.
Lv, Wei
Yang, Chenzi
Shu, Chang
Dardik, Alan
Pericardial Patch Angioplasty Heals via an Ephrin-B2 and CD34 Positive Cell Mediated Mechanism
title Pericardial Patch Angioplasty Heals via an Ephrin-B2 and CD34 Positive Cell Mediated Mechanism
title_full Pericardial Patch Angioplasty Heals via an Ephrin-B2 and CD34 Positive Cell Mediated Mechanism
title_fullStr Pericardial Patch Angioplasty Heals via an Ephrin-B2 and CD34 Positive Cell Mediated Mechanism
title_full_unstemmed Pericardial Patch Angioplasty Heals via an Ephrin-B2 and CD34 Positive Cell Mediated Mechanism
title_short Pericardial Patch Angioplasty Heals via an Ephrin-B2 and CD34 Positive Cell Mediated Mechanism
title_sort pericardial patch angioplasty heals via an ephrin-b2 and cd34 positive cell mediated mechanism
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3374760/
https://www.ncbi.nlm.nih.gov/pubmed/22719962
http://dx.doi.org/10.1371/journal.pone.0038844
work_keys_str_mv AT lixin pericardialpatchangioplastyhealsviaanephrinb2andcd34positivecellmediatedmechanism
AT jadlowieccaroline pericardialpatchangioplastyhealsviaanephrinb2andcd34positivecellmediatedmechanism
AT guoyuanyuan pericardialpatchangioplastyhealsviaanephrinb2andcd34positivecellmediatedmechanism
AT protackclintond pericardialpatchangioplastyhealsviaanephrinb2andcd34positivecellmediatedmechanism
AT zieglerkennethr pericardialpatchangioplastyhealsviaanephrinb2andcd34positivecellmediatedmechanism
AT lvwei pericardialpatchangioplastyhealsviaanephrinb2andcd34positivecellmediatedmechanism
AT yangchenzi pericardialpatchangioplastyhealsviaanephrinb2andcd34positivecellmediatedmechanism
AT shuchang pericardialpatchangioplastyhealsviaanephrinb2andcd34positivecellmediatedmechanism
AT dardikalan pericardialpatchangioplastyhealsviaanephrinb2andcd34positivecellmediatedmechanism