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We are analyzing https://link.springer.com/article/10.1186/s13287-020-01690-y.

Title:
Comparative separation methods and biological characteristics of human placental and umbilical cord mesenchymal stem cells in serum-free culture conditions | Stem Cell Research & Therapy
Description:
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.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {πŸ“š}

  • Science
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Content Management System {πŸ“}

What CMS is link.springer.com built with?

Custom-built

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Traffic Estimate {πŸ“ˆ}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 7,642,828 visitors per month in the current month.

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How Does Link.springer.com Make Money? {πŸ’Έ}

We don't see any clear sign of profit-making.

Many websites are intended to earn money, but some serve to share ideas or build connections. Websites exist for all kinds of purposes. This might be one of them. Link.springer.com might be earning cash quietly, but we haven't detected the monetization method.

Keywords {πŸ”}

cells, mscs, cell, stem, tissue, article, human, mesenchymal, placenta, analysis, placental, culture, google, scholar, method, derived, sources, fig, expression, days, methods, ucmscs, min, characteristics, medium, gene, data, digestion, samples, cas, growth, biological, isolation, differentiation, tissues, number, results, genes, research, umbilical, msc, obtained, secretion, cord, blood, differences, enzymatic, time, compared, membrane,

Topics {βœ’οΈ}

full size image 125-bp/150-bp paired-end reads long-term culture-initiating cells comparative separation methods hand-held electric homogenizer m-mulv reverse transcriptase hand-held homogenizer avoids de groot-swings gm flow cytometric analysis mesenchymal stem cells paired-end cleaned reads stem cell characteristics human mesenchymal stromal human umbilical cord article download pdf serum-free culture conditions amniotic fluid-derived mscs blue-black nissl bodies potential angiogenic effect human placenta-derived cells kcl solution pre-warmed oligo-attached magnetic beads cell expansion decreased serum-free gmp condition scale bar = 200 μm scale bar = 100 μm scale bar = 2 μm umbilical cord blood fenghua liu full access large-scale clinical culture hla-dr writing-original draft preparation organ failure research stem cells dev derived stem cells neonatal tissue-derived msc view primary-cultured cells entered uc-msc-specific region cv-msc-specific region neural stem cells cm-msc-specific region tissue explant method placental tissue-derived mscs human bone marrow understanding high-level functions high-throughput experimental technologies guangdong key research natural science foundation

Questions {❓}

  • Human fetal membranes: a source of stem cells for tissue regeneration and repair?

Schema {πŸ—ΊοΈ}

WebPage:
      mainEntity:
         headline:Comparative separation methods and biological characteristics of human placental and umbilical cord mesenchymal stem cells in serum-free culture conditions
         description: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). 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. 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. 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.
         datePublished:2020-05-19T00:00:00Z
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            Umbilical cord
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            Tissue explant method
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      headline:Comparative separation methods and biological characteristics of human placental and umbilical cord mesenchymal stem cells in serum-free culture conditions
      description: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). 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. 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. 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.
      datePublished:2020-05-19T00:00:00Z
      dateModified:2020-05-19T00:00:00Z
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         Mesenchymal stem cells (MSCs)
         Umbilical cord
         Cell culture
         Tissue explant method
         Enzymatic digestion
         Biological characteristics
         Cell separation methods
         Human placenta
         Stem Cells
         Cell Biology
         Regenerative Medicine/Tissue Engineering
         Biomedical Engineering and Bioengineering
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            name:Feng Chen
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               type:PostalAddress
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      name:Fenghua Liu
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      name:Qing Peng
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            name:Southern Medical University
            address:
               name:Department 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 University, Guangzhou, China
               type:PostalAddress
            type:Organization
      name:Yang Li
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            name:Southern Medical University
            address:
               name:Department 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 University, Guangzhou, China
               type:PostalAddress
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            name:Southern Medical University
            address:
               name:Department 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 University, Guangzhou, China
               type:PostalAddress
            type:Organization
      name:Jiang Du
      affiliation:
            name:Southern Medical University
            address:
               name:Department 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 University, Guangzhou, China
               type:PostalAddress
            type:Organization
      name:Yi Gao
      affiliation:
            name:Zhujiang Hospital, Southern Medical University
            address:
               name:Department of Gynecology, Zhujiang Hospital, Southern Medical University, Guangzhou, China
               type:PostalAddress
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            name:Southern Medical University
            address:
               name:Department 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 University, Guangzhou, China
               type:PostalAddress
            type:Organization
            name:Southern Medical University
            address:
               name:State Key Laboratory of Organ Failure Research, Southern Medical University, Guangzhou, China
               type:PostalAddress
            type:Organization
      email:[email protected]
      name:Yifeng Wang
      url:http://orcid.org/0000-0002-9559-7211
      affiliation:
            name:Zhujiang Hospital, Southern Medical University
            address:
               name:Department of Gynecology, Zhujiang Hospital, Southern Medical University, Guangzhou, China
               type:PostalAddress
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PostalAddress:
      name:Department of Gynecology, Zhujiang Hospital, Southern Medical University, Guangzhou, China
      name:Department of Gynecology, Zhujiang Hospital, Southern Medical University, Guangzhou, China
      name:Department of Reproductive Medicine Center, Provincial Maternal and Child Health Hospital, Guangzhou, China
      name:Department 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 University, Guangzhou, China
      name:Department 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 University, Guangzhou, China
      name:Department 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 University, Guangzhou, China
      name:Department 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 University, Guangzhou, China
      name:Department of Gynecology, Zhujiang Hospital, Southern Medical University, Guangzhou, China
      name:Department 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 University, Guangzhou, China
      name:State Key Laboratory of Organ Failure Research, Southern Medical University, Guangzhou, China
      name:Department of Gynecology, Zhujiang Hospital, Southern Medical University, Guangzhou, China

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