Systemically transplanted mesenchymal stem cells induce vascular-like structure formation in a rat model of vaginal injury.

The beneficial effect of mesenchymal stem cells (MSCs) on wound healing is mostly attributed to a trophic effect that promotes angiogenesis. Whether MSCs can contribute to the formation of new blood vessels by direct differentiation is still controversial. Pelvic floor dysfunction (PFD) is a group o...

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Main Authors: Ofra Ben Menachem-Zidon, Michal Gropp, Etti Ben Shushan, Benjamin Reubinoff, David Shveiky
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0218081
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spelling doaj-d10fd97758d74d3ba49ab968b8c8028e2021-03-03T20:37:49ZengPublic Library of Science (PLoS)PLoS ONE1932-62032019-01-01146e021808110.1371/journal.pone.0218081Systemically transplanted mesenchymal stem cells induce vascular-like structure formation in a rat model of vaginal injury.Ofra Ben Menachem-ZidonMichal GroppEtti Ben ShushanBenjamin ReubinoffDavid ShveikyThe beneficial effect of mesenchymal stem cells (MSCs) on wound healing is mostly attributed to a trophic effect that promotes angiogenesis. Whether MSCs can contribute to the formation of new blood vessels by direct differentiation is still controversial. Pelvic floor dysfunction (PFD) is a group of disorders that negatively affect the quality of women's lives. Traditional vaginal surgical repair provides disappointing anatomical outcome. Stem cell transplantation may be used to supplement surgery and improve its outcome. Here we aimed to examine the engraftment, survival, differentiation and angiogenic effect of transplanted MSCs in a vaginal injury rat model. MSCs were obtained from the bone marrow of Sprague Drawley (SD) rats, expanded and characterized in vitro. The MSCs expressed CD90 and CD29, did not express CD45, CD34, CD11b and CD31 and could differentiate into osteogenic, chondrogenic and adipogenic lineages. Cells were labeled with either PKH-26 or GFP and transplanted systemically or locally to female SD rats, just after a standardized vaginal incision was made. Engraftment after local transplantation was less efficient at all-time points compared to systemic administration. In the systemically transplanted animal group, MSCs migrated to the injury site and were present in the healed vagina for at least 30 days. Both systemic and local MSCs transplantation promoted host angiogenesis. Systemically transplanted MSCs created new vascular-like structures by direct differentiation into endothelium. These findings pave the way to further studies of the potential role of MSCs transplantation in improving surgical outcome in women with PFD.https://doi.org/10.1371/journal.pone.0218081
collection DOAJ
language English
format Article
sources DOAJ
author Ofra Ben Menachem-Zidon
Michal Gropp
Etti Ben Shushan
Benjamin Reubinoff
David Shveiky
spellingShingle Ofra Ben Menachem-Zidon
Michal Gropp
Etti Ben Shushan
Benjamin Reubinoff
David Shveiky
Systemically transplanted mesenchymal stem cells induce vascular-like structure formation in a rat model of vaginal injury.
PLoS ONE
author_facet Ofra Ben Menachem-Zidon
Michal Gropp
Etti Ben Shushan
Benjamin Reubinoff
David Shveiky
author_sort Ofra Ben Menachem-Zidon
title Systemically transplanted mesenchymal stem cells induce vascular-like structure formation in a rat model of vaginal injury.
title_short Systemically transplanted mesenchymal stem cells induce vascular-like structure formation in a rat model of vaginal injury.
title_full Systemically transplanted mesenchymal stem cells induce vascular-like structure formation in a rat model of vaginal injury.
title_fullStr Systemically transplanted mesenchymal stem cells induce vascular-like structure formation in a rat model of vaginal injury.
title_full_unstemmed Systemically transplanted mesenchymal stem cells induce vascular-like structure formation in a rat model of vaginal injury.
title_sort systemically transplanted mesenchymal stem cells induce vascular-like structure formation in a rat model of vaginal injury.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2019-01-01
description The beneficial effect of mesenchymal stem cells (MSCs) on wound healing is mostly attributed to a trophic effect that promotes angiogenesis. Whether MSCs can contribute to the formation of new blood vessels by direct differentiation is still controversial. Pelvic floor dysfunction (PFD) is a group of disorders that negatively affect the quality of women's lives. Traditional vaginal surgical repair provides disappointing anatomical outcome. Stem cell transplantation may be used to supplement surgery and improve its outcome. Here we aimed to examine the engraftment, survival, differentiation and angiogenic effect of transplanted MSCs in a vaginal injury rat model. MSCs were obtained from the bone marrow of Sprague Drawley (SD) rats, expanded and characterized in vitro. The MSCs expressed CD90 and CD29, did not express CD45, CD34, CD11b and CD31 and could differentiate into osteogenic, chondrogenic and adipogenic lineages. Cells were labeled with either PKH-26 or GFP and transplanted systemically or locally to female SD rats, just after a standardized vaginal incision was made. Engraftment after local transplantation was less efficient at all-time points compared to systemic administration. In the systemically transplanted animal group, MSCs migrated to the injury site and were present in the healed vagina for at least 30 days. Both systemic and local MSCs transplantation promoted host angiogenesis. Systemically transplanted MSCs created new vascular-like structures by direct differentiation into endothelium. These findings pave the way to further studies of the potential role of MSCs transplantation in improving surgical outcome in women with PFD.
url https://doi.org/10.1371/journal.pone.0218081
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