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The cell surface glycosphingolipids SSEA-3 and SSEA-4 are not essential for human ESC pluripotency.

The cell surface glycosphingolipids SSEA-3 and SSEA-4 are not essential for human ESC pluripotency. Research Abstract Details 

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  • The cell surface glycosphingolipids SSEA-3 and SSEA-4 are not essential for human ESC pluripotency. Abstract Text:

    sandii n brimbleSandii N Brimble,eric s sherrerEric S Sherrer,elizabeth w uhlElizabeth W Uhl,elaine wangElaine Wang,samuel kellySamuel Kelly,alfred h merrillAlfred H Merrill,allan j robinsAllan J Robins,thomas c schulzThomas C Schulz,

    Pluripotent cells can be isolated from the human blastocyst and maintained in culture as self-renewing, undifferentiated, human ESCs (hESCs). These cells are a valuable model of human development in vitro and are the focus of substantial research aimed at generating differentiated populations for cellular therapies. The extracellular markers that have been used to characterize hESCs are primarily carbohydrate epitopes on proteoglycans or sphingolipids, such as stage-specific embryonic antigen (SSEA)-3 and -4. The expression of SSEA-3 and -4 is tightly regulated during preimplantation development and on hESCs. Although this might imply a molecular function in undifferentiated cells, it has not yet been tested experimentally. We used inhibitors of sphingolipid and glycosphingolipid (GSL) biosynthesis to block the generation of SSEA-3 and -4 in hESCs. Depletion of these antigens and their precursors was confirmed using immunostaining, flow cytometry, and tandem mass spectroscopy. Transcriptional analysis, immunostaining, and differentiation in vitro and in teratomas indicated that other properties of pluripotency were not noticeably affected by GSL depletion. These experiments demonstrated that the GSLs recognized as SSEA-3 and -4 do not play critical functional roles in maintaining the pluripotency of hESCs, but instead suggested roles for this class of molecules during cellular differentiation.

    The cell surface glycosphingolipids SSEA-3 and SSEA-4 are not essential for human ESC pluripotency. Publishing Authors By Initials

    sn brimbleSN Brimble,es sherrerES Sherrer,ew uhlEW Uhl,e wangE Wang,s kellyS Kelly,ah merrillAH Merrill,aj robinsAJ Robins,tc schulzTC Schulz,

    For similar cells: stem cells: pluripotent stem cells research abstracts see: cells: stem cells: pluripotent stem cells research

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    The cell surface glycosphingolipids SSEA-3 and SSEA-4 are not essential for human ESC pluripotency. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: Stem cells (Dayton, Ohio)

    VOLUME: 25

    Page Numbers: 54-62

    Journal Abbreviation: Stem Cells

    ISSN: 1066-5099

    DAY: 28

    MONTH: 09

    YEAR: 2006

    The cell surface glycosphingolipids SSEA-3 and SSEA-4 are not essential for human ESC pluripotency. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9304532

    The cell surface glycosphingolipids SSEA-3 and SSEA-4 are not essential for human ESC pluripotency. Keywords Mesh Terms:

    KEYWORDS: Pluripotent Stem Cells

    MESH TERMS: physiology

    Chemical & Substance for Abstract: The cell surface glycosphingolipids SSEA-3 and SSEA-4 are not essential for human ESC pluripotency. Information

    Substance Name: stage-specific embryonic antigen 4

    Registry Number: 0

    Grant and Affiliation Information for The cell surface glycosphingolipids SSEA-3 and SSEA-4 are not essential for human ESC pluripotency.

    AFFILIATION: Novocell, Athens, Georgia, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NCRR

    GRANT: R24RR021313-05

    ACRONYM: RR

    MEDLINETA: Stem Cells

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    ACCESSION NUMBER:

    Number Hits: 0

    The cell surface glycosphingolipids SSEA-3 and SSEA-4 are not essential for human ESC pluripotency Related Publications

     

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