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...
Main Authors: | , , , , |
---|---|
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 |
id |
doaj-d10fd97758d74d3ba49ab968b8c8028e |
---|---|
record_format |
Article |
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 |
work_keys_str_mv |
AT ofrabenmenachemzidon systemicallytransplantedmesenchymalstemcellsinducevascularlikestructureformationinaratmodelofvaginalinjury AT michalgropp systemicallytransplantedmesenchymalstemcellsinducevascularlikestructureformationinaratmodelofvaginalinjury AT ettibenshushan systemicallytransplantedmesenchymalstemcellsinducevascularlikestructureformationinaratmodelofvaginalinjury AT benjaminreubinoff systemicallytransplantedmesenchymalstemcellsinducevascularlikestructureformationinaratmodelofvaginalinjury AT davidshveiky systemicallytransplantedmesenchymalstemcellsinducevascularlikestructureformationinaratmodelofvaginalinjury |
_version_ |
1714821452109185024 |