Cargando…

Tracing GFP-labeled WJMSCs in vivo using a chronic salpingitis model: an animal experiment

BACKGROUND: The present study was conducted to evaluate the distribution of Wharton’s jelly-derived mesenchymal stem cells (WJMSCs) and their repairing function on the oviduct. METHODS: WJMSCs were transfected with the LV3-GFP-PURO lentivirus. Female New Zealand rabbits (n = 24) were divided randoml...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Zhe, Zhang, Zhao, Ming, Wai-kit, Chen, Xin, Xiao, Xiao-min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5709981/
https://www.ncbi.nlm.nih.gov/pubmed/29191249
http://dx.doi.org/10.1186/s13287-017-0714-z
_version_ 1783282890975477760
author Li, Zhe
Zhang, Zhao
Ming, Wai-kit
Chen, Xin
Xiao, Xiao-min
author_facet Li, Zhe
Zhang, Zhao
Ming, Wai-kit
Chen, Xin
Xiao, Xiao-min
author_sort Li, Zhe
collection PubMed
description BACKGROUND: The present study was conducted to evaluate the distribution of Wharton’s jelly-derived mesenchymal stem cells (WJMSCs) and their repairing function on the oviduct. METHODS: WJMSCs were transfected with the LV3-GFP-PURO lentivirus. Female New Zealand rabbits (n = 24) were divided randomly into control A and B groups and experimental C and D groups to establish inflammation models. Sterile saline solution or WJMSCs were injected into rabbits via ear veins and/or genital tract perfusion once weekly for 3 weeks. All rabbits were humanely sacrificed 1 week after the last perfusion to collect the oviduct, uterus, liver, and bladder for examination. Green fluorescent protein (GFP) and cytokeratin 7 (CK7) were imaged using a Leica Qwin Plus V3 fluorescence confocal microscope and analyzed as mean optical densities in an Image-Pro Plus analysis system. RESULTS: We found that lentivirus expressing the GFP gene produced an efficient transfection. The mean optical density values of GFP and CK7 in the oviducts were higher in the experimental D group than those in the control A and experimental C groups. No GFP fluorescence deposits occurred in the bladder of the control A group or experimental C group. Colocalization of CK7 and WJMSCs was observed in the oviducts in all groups. CONCLUSIONS: WJMSCs exhibited homing characteristics and migrated to the injured oviduct to promote epithelial cell growth. Additionally, local treatment resulted in higher efficiency.
format Online
Article
Text
id pubmed-5709981
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-57099812017-12-06 Tracing GFP-labeled WJMSCs in vivo using a chronic salpingitis model: an animal experiment Li, Zhe Zhang, Zhao Ming, Wai-kit Chen, Xin Xiao, Xiao-min Stem Cell Res Ther Research BACKGROUND: The present study was conducted to evaluate the distribution of Wharton’s jelly-derived mesenchymal stem cells (WJMSCs) and their repairing function on the oviduct. METHODS: WJMSCs were transfected with the LV3-GFP-PURO lentivirus. Female New Zealand rabbits (n = 24) were divided randomly into control A and B groups and experimental C and D groups to establish inflammation models. Sterile saline solution or WJMSCs were injected into rabbits via ear veins and/or genital tract perfusion once weekly for 3 weeks. All rabbits were humanely sacrificed 1 week after the last perfusion to collect the oviduct, uterus, liver, and bladder for examination. Green fluorescent protein (GFP) and cytokeratin 7 (CK7) were imaged using a Leica Qwin Plus V3 fluorescence confocal microscope and analyzed as mean optical densities in an Image-Pro Plus analysis system. RESULTS: We found that lentivirus expressing the GFP gene produced an efficient transfection. The mean optical density values of GFP and CK7 in the oviducts were higher in the experimental D group than those in the control A and experimental C groups. No GFP fluorescence deposits occurred in the bladder of the control A group or experimental C group. Colocalization of CK7 and WJMSCs was observed in the oviducts in all groups. CONCLUSIONS: WJMSCs exhibited homing characteristics and migrated to the injured oviduct to promote epithelial cell growth. Additionally, local treatment resulted in higher efficiency. BioMed Central 2017-12-01 /pmc/articles/PMC5709981/ /pubmed/29191249 http://dx.doi.org/10.1186/s13287-017-0714-z Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Li, Zhe
Zhang, Zhao
Ming, Wai-kit
Chen, Xin
Xiao, Xiao-min
Tracing GFP-labeled WJMSCs in vivo using a chronic salpingitis model: an animal experiment
title Tracing GFP-labeled WJMSCs in vivo using a chronic salpingitis model: an animal experiment
title_full Tracing GFP-labeled WJMSCs in vivo using a chronic salpingitis model: an animal experiment
title_fullStr Tracing GFP-labeled WJMSCs in vivo using a chronic salpingitis model: an animal experiment
title_full_unstemmed Tracing GFP-labeled WJMSCs in vivo using a chronic salpingitis model: an animal experiment
title_short Tracing GFP-labeled WJMSCs in vivo using a chronic salpingitis model: an animal experiment
title_sort tracing gfp-labeled wjmscs in vivo using a chronic salpingitis model: an animal experiment
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5709981/
https://www.ncbi.nlm.nih.gov/pubmed/29191249
http://dx.doi.org/10.1186/s13287-017-0714-z
work_keys_str_mv AT lizhe tracinggfplabeledwjmscsinvivousingachronicsalpingitismodelananimalexperiment
AT zhangzhao tracinggfplabeledwjmscsinvivousingachronicsalpingitismodelananimalexperiment
AT mingwaikit tracinggfplabeledwjmscsinvivousingachronicsalpingitismodelananimalexperiment
AT chenxin tracinggfplabeledwjmscsinvivousingachronicsalpingitismodelananimalexperiment
AT xiaoxiaomin tracinggfplabeledwjmscsinvivousingachronicsalpingitismodelananimalexperiment