Comparative separation methods and biological characteristics of human placental and umbilical cord mesenchymal stem cells in serum-free culture conditions

Abstract Background Mesenchymal stem cells (MSCs) are considered to be an effective tool for regenerative medicine with promising applications for clinical therapy. However, incongruent data has been reported partially owing to their functional heterogeneity. To provide sufficient and suitable clini...

Full description

Bibliographic Details
Main Authors: Xiao Yi, Feng Chen, Fenghua Liu, Qing Peng, Yang Li, Shao Li, Jiang Du, Yi Gao, Yifeng Wang
Format: Article
Language:English
Published: BMC 2020-05-01
Series:Stem Cell Research & Therapy
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13287-020-01690-y
_version_ 1818891738167640064
author Xiao Yi
Feng Chen
Fenghua Liu
Qing Peng
Yang Li
Shao Li
Jiang Du
Yi Gao
Yifeng Wang
author_facet Xiao Yi
Feng Chen
Fenghua Liu
Qing Peng
Yang Li
Shao Li
Jiang Du
Yi Gao
Yifeng Wang
author_sort Xiao Yi
collection DOAJ
description Abstract Background Mesenchymal stem cells (MSCs) are considered to be an effective tool for regenerative medicine with promising applications for clinical therapy. However, incongruent data has been reported partially owing to their functional heterogeneity. To provide sufficient and suitable clinical seed cells derived from the placenta for MSC therapy, we compared the various current isolation methods, as well as the biological characteristics, of different human placenta mesenchymal stem cells (hPMSCs). Methods We selected placentas from 35 informed donors and exploited three commonly used methods. MSCs were isolated from different parts of placental tissue including umbilical cord (UC), amniotic membrane (AM), chorionic membrane (CM), chorionic villi (CV), and deciduae (DC). The appropriate isolation methods for each type of hPMSCs were first assessed. The resulting five MSC types from the same individuals were identified based on their surface marker expression, proliferation capacity, transcriptome, differentiation, multipotency and karyotype. Results All three methods successfully isolated the five hPMSC types from placental tissues. However, the UC-MSCs were most effectively separated via the tissue explant method, while the enzymatic digestion method was found to be more suitable for separating CV-MSCs, owing to its higher output efficiency compared to the other methods. Alternatively, the perfusion method was complicated and exhibited the lowest efficiency for cell isolation and uniformity. Furthermore, we determined that UC-MSCs and CV-MSCs express a higher level of paracrine cytokines and display much stronger proliferative capacity as well as superior extraction efficiency. Finally, karyotype analysis revealed that DC-MSCs are derived from the mother, while the other cell types are derived from the fetus. Moreover, the different hPMSCs exhibited unique gene expression profiles, which may prove advantageous in treatment of a broad range of diseases. Conclusions hPMSCs from different sources are similar yet also unique. Our results describe the biological characteristics of five hPMSCs and provide insights to aide in the selection process of candidates for MSCs treatment. Overall, UC- and CV-MSCs appear to be ideal sources of primary MSCs for clinical treatment and future research.
first_indexed 2024-12-19T17:45:34Z
format Article
id doaj.art-bdef1cb4fe384e2b8c81fa0f0b8d35ca
institution Directory Open Access Journal
issn 1757-6512
language English
last_indexed 2024-12-19T17:45:34Z
publishDate 2020-05-01
publisher BMC
record_format Article
series Stem Cell Research & Therapy
spelling doaj.art-bdef1cb4fe384e2b8c81fa0f0b8d35ca2022-12-21T20:12:05ZengBMCStem Cell Research & Therapy1757-65122020-05-0111111510.1186/s13287-020-01690-yComparative separation methods and biological characteristics of human placental and umbilical cord mesenchymal stem cells in serum-free culture conditionsXiao Yi0Feng Chen1Fenghua Liu2Qing Peng3Yang Li4Shao Li5Jiang Du6Yi Gao7Yifeng Wang8Department of Gynecology, Zhujiang Hospital, Southern Medical UniversityDepartment of Gynecology, Zhujiang Hospital, Southern Medical UniversityDepartment of Reproductive Medicine Center, Provincial Maternal and Child Health HospitalDepartment of Hepatobiliary Surgery II, Guangdong Provincial Research Center for Artificial Organ and Tissue Engineering, Guangzhou Clinical Research and Transformation Center for Artificial Liver, Institute of Regenerative Medicine, Zhujiang Hospital, Southern Medical UniversityDepartment of Hepatobiliary Surgery II, Guangdong Provincial Research Center for Artificial Organ and Tissue Engineering, Guangzhou Clinical Research and Transformation Center for Artificial Liver, Institute of Regenerative Medicine, Zhujiang Hospital, Southern Medical UniversityDepartment of Hepatobiliary Surgery II, Guangdong Provincial Research Center for Artificial Organ and Tissue Engineering, Guangzhou Clinical Research and Transformation Center for Artificial Liver, Institute of Regenerative Medicine, Zhujiang Hospital, Southern Medical UniversityDepartment of Hepatobiliary Surgery II, Guangdong Provincial Research Center for Artificial Organ and Tissue Engineering, Guangzhou Clinical Research and Transformation Center for Artificial Liver, Institute of Regenerative Medicine, Zhujiang Hospital, Southern Medical UniversityDepartment of Gynecology, Zhujiang Hospital, Southern Medical UniversityDepartment of Gynecology, Zhujiang Hospital, Southern Medical UniversityAbstract Background Mesenchymal stem cells (MSCs) are considered to be an effective tool for regenerative medicine with promising applications for clinical therapy. However, incongruent data has been reported partially owing to their functional heterogeneity. To provide sufficient and suitable clinical seed cells derived from the placenta for MSC therapy, we compared the various current isolation methods, as well as the biological characteristics, of different human placenta mesenchymal stem cells (hPMSCs). Methods We selected placentas from 35 informed donors and exploited three commonly used methods. MSCs were isolated from different parts of placental tissue including umbilical cord (UC), amniotic membrane (AM), chorionic membrane (CM), chorionic villi (CV), and deciduae (DC). The appropriate isolation methods for each type of hPMSCs were first assessed. The resulting five MSC types from the same individuals were identified based on their surface marker expression, proliferation capacity, transcriptome, differentiation, multipotency and karyotype. Results All three methods successfully isolated the five hPMSC types from placental tissues. However, the UC-MSCs were most effectively separated via the tissue explant method, while the enzymatic digestion method was found to be more suitable for separating CV-MSCs, owing to its higher output efficiency compared to the other methods. Alternatively, the perfusion method was complicated and exhibited the lowest efficiency for cell isolation and uniformity. Furthermore, we determined that UC-MSCs and CV-MSCs express a higher level of paracrine cytokines and display much stronger proliferative capacity as well as superior extraction efficiency. Finally, karyotype analysis revealed that DC-MSCs are derived from the mother, while the other cell types are derived from the fetus. Moreover, the different hPMSCs exhibited unique gene expression profiles, which may prove advantageous in treatment of a broad range of diseases. Conclusions hPMSCs from different sources are similar yet also unique. Our results describe the biological characteristics of five hPMSCs and provide insights to aide in the selection process of candidates for MSCs treatment. Overall, UC- and CV-MSCs appear to be ideal sources of primary MSCs for clinical treatment and future research.http://link.springer.com/article/10.1186/s13287-020-01690-yMesenchymal stem cells (MSCs)Umbilical cordCell cultureTissue explant methodEnzymatic digestionBiological characteristics
spellingShingle Xiao Yi
Feng Chen
Fenghua Liu
Qing Peng
Yang Li
Shao Li
Jiang Du
Yi Gao
Yifeng Wang
Comparative separation methods and biological characteristics of human placental and umbilical cord mesenchymal stem cells in serum-free culture conditions
Stem Cell Research & Therapy
Mesenchymal stem cells (MSCs)
Umbilical cord
Cell culture
Tissue explant method
Enzymatic digestion
Biological characteristics
title Comparative separation methods and biological characteristics of human placental and umbilical cord mesenchymal stem cells in serum-free culture conditions
title_full Comparative separation methods and biological characteristics of human placental and umbilical cord mesenchymal stem cells in serum-free culture conditions
title_fullStr Comparative separation methods and biological characteristics of human placental and umbilical cord mesenchymal stem cells in serum-free culture conditions
title_full_unstemmed Comparative separation methods and biological characteristics of human placental and umbilical cord mesenchymal stem cells in serum-free culture conditions
title_short Comparative separation methods and biological characteristics of human placental and umbilical cord mesenchymal stem cells in serum-free culture conditions
title_sort comparative separation methods and biological characteristics of human placental and umbilical cord mesenchymal stem cells in serum free culture conditions
topic Mesenchymal stem cells (MSCs)
Umbilical cord
Cell culture
Tissue explant method
Enzymatic digestion
Biological characteristics
url http://link.springer.com/article/10.1186/s13287-020-01690-y
work_keys_str_mv AT xiaoyi comparativeseparationmethodsandbiologicalcharacteristicsofhumanplacentalandumbilicalcordmesenchymalstemcellsinserumfreecultureconditions
AT fengchen comparativeseparationmethodsandbiologicalcharacteristicsofhumanplacentalandumbilicalcordmesenchymalstemcellsinserumfreecultureconditions
AT fenghualiu comparativeseparationmethodsandbiologicalcharacteristicsofhumanplacentalandumbilicalcordmesenchymalstemcellsinserumfreecultureconditions
AT qingpeng comparativeseparationmethodsandbiologicalcharacteristicsofhumanplacentalandumbilicalcordmesenchymalstemcellsinserumfreecultureconditions
AT yangli comparativeseparationmethodsandbiologicalcharacteristicsofhumanplacentalandumbilicalcordmesenchymalstemcellsinserumfreecultureconditions
AT shaoli comparativeseparationmethodsandbiologicalcharacteristicsofhumanplacentalandumbilicalcordmesenchymalstemcellsinserumfreecultureconditions
AT jiangdu comparativeseparationmethodsandbiologicalcharacteristicsofhumanplacentalandumbilicalcordmesenchymalstemcellsinserumfreecultureconditions
AT yigao comparativeseparationmethodsandbiologicalcharacteristicsofhumanplacentalandumbilicalcordmesenchymalstemcellsinserumfreecultureconditions
AT yifengwang comparativeseparationmethodsandbiologicalcharacteristicsofhumanplacentalandumbilicalcordmesenchymalstemcellsinserumfreecultureconditions