Here's how LINK.SPRINGER.COM makes money* and how much!

*Please read our disclaimer before using our estimates.
Loading...

LINK . SPRINGER . COM {}

  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Link.springer.com Make Money
  6. Keywords
  7. Topics
  8. Schema
  9. External Links
  10. Analytics And Tracking
  11. Libraries

We are analyzing https://link.springer.com/article/10.1186/s13287-018-0876-3.

Title:
Changes in phenotype and differentiation potential of human mesenchymal stem cells aging in vitro | Stem Cell Research & Therapy
Description:
Background Adult mesenchymal stem cells (MSCs) hold great promise for regenerative medicine because of their self-renewal, multipotency, and trophic and immunosuppressive effects. Due to the rareness and high heterogeneity of freshly isolated MSCs, extensive in-vitro passage is required to expand their populations prior to clinical use; however, senescence usually accompanies and can potentially affect MSC characteristics and functionality. Therefore, a thorough characterization of the variations in phenotype and differentiation potential of in-vitro aging MSCs must be sought. Methods Human bone marrow-derived MSCs were passaged in vitro and cultivated with either DMEM-based or αMEM-based expansion media. Cells were prepared for subculture every 10 days up to passage 8 and were analyzed for cell morphology, proliferative capacity, and surface marker expression at the end of each passage. The gene expression profile and adipogenic and osteogenic differentiation capability of MSCs at early (passage 4) and late (passage 8) passages were also evaluated. Results In-vitro aging MSCs gradually lost the typical fibroblast-like spindle shape, leading to elevated morphological abnormality and inhomogeneity. While the DMEM-based expansion medium better facilitated MSC proliferation in the early passages, the cell population doubling rate reduced over time in both DMEM and αMEM groups. CD146 expression decreased with increasing passage number only when MSCs were cultured under the DMEM-based condition. Senescence also resulted in MSCs with genetic instability, which was further regulated by the medium recipe. Regardless of the expansion condition, MSCs at both passages 4 and 8 could differentiate into adipocyte-like cells whereas osteogenesis of aged MSCs was significantly compromised. For osteogenic induction, use of the αMEM-based expansion medium yielded longer osteogenesis and better quality. Conclusions Human MSCs subjected to extensive in-vitro passage can undergo morphological, phenotypic, and genetic changes. These properties are also modulated by the medium composition employed to expand the cell populations. In addition, adipogenic potential may be better preserved over osteogenesis in aged MSCs, suggesting that MSCs at early passages must be used for osteogenic differentiation. The current study presents valuable information for future basic science research and clinical applications leading to the development of novel MSC-based therapeutic strategies for different diseases.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Science
  • Non-Profit & Charity

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

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 5,000,019 visitors per month in the current month.
However, some sources were not loaded, we suggest to reload the page to get complete results.

check SE Ranking
check Ahrefs
check Similarweb
check Ubersuggest
check Semrush

How Does Link.springer.com Make Money? {💸}

We can't tell how the site generates income.

Websites don't always need to be profitable; some serve as platforms for education or personal expression. Websites can serve multiple purposes. And this might be one of them. Link.springer.com might be making money, but it's not detectable how they're doing it.

Keywords {🔍}

mscs, cells, pubmed, cell, article, stem, fig, google, scholar, expression, differentiation, msc, osteogenic, cas, human, mesenchymal, aging, medium, bone, adipogenic, dmem, pmscs, invitro, expansion, gene, group, passage, marrow, αmem, groups, passages, fold, days, potential, samples, media, derived, ncpd, condition, telomere, populations, lpl, runx, passaged, αmembased, size, pparγ, genes, central, dmembased,

Topics {✒️}

yueh-hsun kevin yang peptide-functionalized peg-based hydrogels tgf-β1 gene-activated scaffolds human factor ix xeno-free supplement derived real-time quantitative pcr high-dose chemotherapy received colony-forming unit fibroblasts 33\times \log \left article download pdf 50 μg/ml ascorbic acid adipose-derived stromal cells autologous-blood stem cells breast cancer patients 72 mg/ml sodium bicarbonate msc-based therapeutic strategies mesenchymal stromal cells mesenchymal stem cell αmem-based proliferation medium mesenchymal stem cells human bone marrow bone marrow exhibited adult bone marrow adult stem cells full access stromal cells derived bmc cell biol muscle-derived rodent mscs high-glucose dmem supplemented clonal mesenchymal progenitors record cell morphology related subjects stem cell res fifty msc-specific genes cell aging research dmem-based expansion medium αmem-based medium led lineage-dependent differentiation capacity hematopoietic stem cells preserve msc morphology αmem-based expansion condition age-related intrinsic bone marrow failure bone marrow sinusoids recycling stem cells privacy choices/manage cookies αmem-based expansion media dmem-based expansion condition cells undergoing adipogenesis human mscs derived

Schema {🗺️}

WebPage:
      mainEntity:
         headline:Changes in phenotype and differentiation potential of human mesenchymal stem cells aging in vitro
         description:Adult mesenchymal stem cells (MSCs) hold great promise for regenerative medicine because of their self-renewal, multipotency, and trophic and immunosuppressive effects. Due to the rareness and high heterogeneity of freshly isolated MSCs, extensive in-vitro passage is required to expand their populations prior to clinical use; however, senescence usually accompanies and can potentially affect MSC characteristics and functionality. Therefore, a thorough characterization of the variations in phenotype and differentiation potential of in-vitro aging MSCs must be sought. Human bone marrow-derived MSCs were passaged in vitro and cultivated with either DMEM-based or αMEM-based expansion media. Cells were prepared for subculture every 10 days up to passage 8 and were analyzed for cell morphology, proliferative capacity, and surface marker expression at the end of each passage. The gene expression profile and adipogenic and osteogenic differentiation capability of MSCs at early (passage 4) and late (passage 8) passages were also evaluated. In-vitro aging MSCs gradually lost the typical fibroblast-like spindle shape, leading to elevated morphological abnormality and inhomogeneity. While the DMEM-based expansion medium better facilitated MSC proliferation in the early passages, the cell population doubling rate reduced over time in both DMEM and αMEM groups. CD146 expression decreased with increasing passage number only when MSCs were cultured under the DMEM-based condition. Senescence also resulted in MSCs with genetic instability, which was further regulated by the medium recipe. Regardless of the expansion condition, MSCs at both passages 4 and 8 could differentiate into adipocyte-like cells whereas osteogenesis of aged MSCs was significantly compromised. For osteogenic induction, use of the αMEM-based expansion medium yielded longer osteogenesis and better quality. Human MSCs subjected to extensive in-vitro passage can undergo morphological, phenotypic, and genetic changes. These properties are also modulated by the medium composition employed to expand the cell populations. In addition, adipogenic potential may be better preserved over osteogenesis in aged MSCs, suggesting that MSCs at early passages must be used for osteogenic differentiation. The current study presents valuable information for future basic science research and clinical applications leading to the development of novel MSC-based therapeutic strategies for different diseases.
         datePublished:2018-05-11T00:00:00Z
         dateModified:2018-05-11T00:00:00Z
         pageStart:1
         pageEnd:14
         license:http://creativecommons.org/publicdomain/zero/1.0/
         sameAs:https://doi.org/10.1186/s13287-018-0876-3
         keywords:
            Human mesenchymal stem cell
            Aging
            Morphology
            Proliferation
            Differentiation
            Adipogenesis
            Osteogenesis
            CD106
            CD146
            Gene expression
            Stem Cells
            Cell Biology
            Regenerative Medicine/Tissue Engineering
            Biomedical Engineering and Bioengineering
         image:
            https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs13287-018-0876-3/MediaObjects/13287_2018_876_Fig1_HTML.gif
            https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs13287-018-0876-3/MediaObjects/13287_2018_876_Fig2_HTML.gif
            https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs13287-018-0876-3/MediaObjects/13287_2018_876_Fig3_HTML.gif
            https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs13287-018-0876-3/MediaObjects/13287_2018_876_Fig4_HTML.gif
            https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs13287-018-0876-3/MediaObjects/13287_2018_876_Fig5_HTML.gif
            https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs13287-018-0876-3/MediaObjects/13287_2018_876_Fig6_HTML.gif
            https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs13287-018-0876-3/MediaObjects/13287_2018_876_Fig7_HTML.gif
            https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs13287-018-0876-3/MediaObjects/13287_2018_876_Fig8_HTML.gif
            https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs13287-018-0876-3/MediaObjects/13287_2018_876_Fig9_HTML.gif
         isPartOf:
            name:Stem Cell Research & Therapy
            issn:
               1757-6512
            volumeNumber:9
            type:
               Periodical
               PublicationVolume
         publisher:
            name:BioMed Central
            logo:
               url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
               type:ImageObject
            type:Organization
         author:
               name:Yueh-Hsun Kevin Yang
               url:http://orcid.org/0000-0003-0298-8641
               affiliation:
                     name:The City University of New York - the City College
                     address:
                        name:Department of Biomedical Engineering, The City University of New York - the City College, New York, USA
                        type:PostalAddress
                     type:Organization
               email:[email protected]
               type:Person
               name:Courtney R. Ogando
               affiliation:
                     name:The City University of New York - the City College
                     address:
                        name:Department of Biomedical Engineering, The City University of New York - the City College, New York, USA
                        type:PostalAddress
                     type:Organization
               type:Person
               name:Carmine Wang See
               affiliation:
                     name:The City University of New York - the City College
                     address:
                        name:Department of Biomedical Engineering, The City University of New York - the City College, New York, USA
                        type:PostalAddress
                     type:Organization
               type:Person
               name:Tsui-Yun Chang
               affiliation:
                     name:The City University of New York - the City College
                     address:
                        name:Department of Biomedical Engineering, The City University of New York - the City College, New York, USA
                        type:PostalAddress
                     type:Organization
               type:Person
               name:Gilda A. Barabino
               affiliation:
                     name:The City University of New York - the City College
                     address:
                        name:Department of Biomedical Engineering, The City University of New York - the City College, New York, USA
                        type:PostalAddress
                     type:Organization
               type:Person
         isAccessibleForFree:1
         type:ScholarlyArticle
      context:https://schema.org
ScholarlyArticle:
      headline:Changes in phenotype and differentiation potential of human mesenchymal stem cells aging in vitro
      description:Adult mesenchymal stem cells (MSCs) hold great promise for regenerative medicine because of their self-renewal, multipotency, and trophic and immunosuppressive effects. Due to the rareness and high heterogeneity of freshly isolated MSCs, extensive in-vitro passage is required to expand their populations prior to clinical use; however, senescence usually accompanies and can potentially affect MSC characteristics and functionality. Therefore, a thorough characterization of the variations in phenotype and differentiation potential of in-vitro aging MSCs must be sought. Human bone marrow-derived MSCs were passaged in vitro and cultivated with either DMEM-based or αMEM-based expansion media. Cells were prepared for subculture every 10 days up to passage 8 and were analyzed for cell morphology, proliferative capacity, and surface marker expression at the end of each passage. The gene expression profile and adipogenic and osteogenic differentiation capability of MSCs at early (passage 4) and late (passage 8) passages were also evaluated. In-vitro aging MSCs gradually lost the typical fibroblast-like spindle shape, leading to elevated morphological abnormality and inhomogeneity. While the DMEM-based expansion medium better facilitated MSC proliferation in the early passages, the cell population doubling rate reduced over time in both DMEM and αMEM groups. CD146 expression decreased with increasing passage number only when MSCs were cultured under the DMEM-based condition. Senescence also resulted in MSCs with genetic instability, which was further regulated by the medium recipe. Regardless of the expansion condition, MSCs at both passages 4 and 8 could differentiate into adipocyte-like cells whereas osteogenesis of aged MSCs was significantly compromised. For osteogenic induction, use of the αMEM-based expansion medium yielded longer osteogenesis and better quality. Human MSCs subjected to extensive in-vitro passage can undergo morphological, phenotypic, and genetic changes. These properties are also modulated by the medium composition employed to expand the cell populations. In addition, adipogenic potential may be better preserved over osteogenesis in aged MSCs, suggesting that MSCs at early passages must be used for osteogenic differentiation. The current study presents valuable information for future basic science research and clinical applications leading to the development of novel MSC-based therapeutic strategies for different diseases.
      datePublished:2018-05-11T00:00:00Z
      dateModified:2018-05-11T00:00:00Z
      pageStart:1
      pageEnd:14
      license:http://creativecommons.org/publicdomain/zero/1.0/
      sameAs:https://doi.org/10.1186/s13287-018-0876-3
      keywords:
         Human mesenchymal stem cell
         Aging
         Morphology
         Proliferation
         Differentiation
         Adipogenesis
         Osteogenesis
         CD106
         CD146
         Gene expression
         Stem Cells
         Cell Biology
         Regenerative Medicine/Tissue Engineering
         Biomedical Engineering and Bioengineering
      image:
         https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs13287-018-0876-3/MediaObjects/13287_2018_876_Fig1_HTML.gif
         https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs13287-018-0876-3/MediaObjects/13287_2018_876_Fig2_HTML.gif
         https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs13287-018-0876-3/MediaObjects/13287_2018_876_Fig3_HTML.gif
         https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs13287-018-0876-3/MediaObjects/13287_2018_876_Fig4_HTML.gif
         https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs13287-018-0876-3/MediaObjects/13287_2018_876_Fig5_HTML.gif
         https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs13287-018-0876-3/MediaObjects/13287_2018_876_Fig6_HTML.gif
         https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs13287-018-0876-3/MediaObjects/13287_2018_876_Fig7_HTML.gif
         https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs13287-018-0876-3/MediaObjects/13287_2018_876_Fig8_HTML.gif
         https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs13287-018-0876-3/MediaObjects/13287_2018_876_Fig9_HTML.gif
      isPartOf:
         name:Stem Cell Research & Therapy
         issn:
            1757-6512
         volumeNumber:9
         type:
            Periodical
            PublicationVolume
      publisher:
         name:BioMed Central
         logo:
            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
            type:ImageObject
         type:Organization
      author:
            name:Yueh-Hsun Kevin Yang
            url:http://orcid.org/0000-0003-0298-8641
            affiliation:
                  name:The City University of New York - the City College
                  address:
                     name:Department of Biomedical Engineering, The City University of New York - the City College, New York, USA
                     type:PostalAddress
                  type:Organization
            email:[email protected]
            type:Person
            name:Courtney R. Ogando
            affiliation:
                  name:The City University of New York - the City College
                  address:
                     name:Department of Biomedical Engineering, The City University of New York - the City College, New York, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Carmine Wang See
            affiliation:
                  name:The City University of New York - the City College
                  address:
                     name:Department of Biomedical Engineering, The City University of New York - the City College, New York, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Tsui-Yun Chang
            affiliation:
                  name:The City University of New York - the City College
                  address:
                     name:Department of Biomedical Engineering, The City University of New York - the City College, New York, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Gilda A. Barabino
            affiliation:
                  name:The City University of New York - the City College
                  address:
                     name:Department of Biomedical Engineering, The City University of New York - the City College, New York, USA
                     type:PostalAddress
                  type:Organization
            type:Person
      isAccessibleForFree:1
["Periodical","PublicationVolume"]:
      name:Stem Cell Research & Therapy
      issn:
         1757-6512
      volumeNumber:9
Organization:
      name:BioMed Central
      logo:
         url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
         type:ImageObject
      name:The City University of New York - the City College
      address:
         name:Department of Biomedical Engineering, The City University of New York - the City College, New York, USA
         type:PostalAddress
      name:The City University of New York - the City College
      address:
         name:Department of Biomedical Engineering, The City University of New York - the City College, New York, USA
         type:PostalAddress
      name:The City University of New York - the City College
      address:
         name:Department of Biomedical Engineering, The City University of New York - the City College, New York, USA
         type:PostalAddress
      name:The City University of New York - the City College
      address:
         name:Department of Biomedical Engineering, The City University of New York - the City College, New York, USA
         type:PostalAddress
      name:The City University of New York - the City College
      address:
         name:Department of Biomedical Engineering, The City University of New York - the City College, New York, USA
         type:PostalAddress
ImageObject:
      url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
Person:
      name:Yueh-Hsun Kevin Yang
      url:http://orcid.org/0000-0003-0298-8641
      affiliation:
            name:The City University of New York - the City College
            address:
               name:Department of Biomedical Engineering, The City University of New York - the City College, New York, USA
               type:PostalAddress
            type:Organization
      email:[email protected]
      name:Courtney R. Ogando
      affiliation:
            name:The City University of New York - the City College
            address:
               name:Department of Biomedical Engineering, The City University of New York - the City College, New York, USA
               type:PostalAddress
            type:Organization
      name:Carmine Wang See
      affiliation:
            name:The City University of New York - the City College
            address:
               name:Department of Biomedical Engineering, The City University of New York - the City College, New York, USA
               type:PostalAddress
            type:Organization
      name:Tsui-Yun Chang
      affiliation:
            name:The City University of New York - the City College
            address:
               name:Department of Biomedical Engineering, The City University of New York - the City College, New York, USA
               type:PostalAddress
            type:Organization
      name:Gilda A. Barabino
      affiliation:
            name:The City University of New York - the City College
            address:
               name:Department of Biomedical Engineering, The City University of New York - the City College, New York, USA
               type:PostalAddress
            type:Organization
PostalAddress:
      name:Department of Biomedical Engineering, The City University of New York - the City College, New York, USA
      name:Department of Biomedical Engineering, The City University of New York - the City College, New York, USA
      name:Department of Biomedical Engineering, The City University of New York - the City College, New York, USA
      name:Department of Biomedical Engineering, The City University of New York - the City College, New York, USA
      name:Department of Biomedical Engineering, The City University of New York - the City College, New York, USA

External Links {🔗}(205)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js
  • Prism.js

4.38s.