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Disruption of apical-basal polarity of human embryonic stem cells enhances hematoendothelial differentiation.

Disruption of apical-basal polarity of human embryonic stem cells enhances hematoendothelial differentiation. Research Abstract Details 

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  • Disruption of apical-basal polarity of human embryonic stem cells enhances hematoendothelial differentiation. Abstract Text:

    ana krtolicaAna Krtolica,olga genbacevOlga Genbacev,carmen escobedoCarmen Escobedo,tamara zdravkovicTamara Zdravkovic,adam nordstromAdam Nordstrom,diana vabuenaDiana Vabuena,aneel nathAneel Nath,carlos simonCarlos Simon,keith mostovKeith Mostov,susan j fisherSusan J Fisher,

    During murine development, the formation of tight junctions and acquisition of polarity are associated with allocation of the blastomeres on the outer surface of the embryo to the trophoblast lineage, whereas the absence of polarization directs cells to the inner cell mass. Here, we report the results of ultrastructural analyses that suggest a similar link between polarization and cell fate in human embryos. In contrast, the five human embryonic stem cell (hESC) lines displayed apical-basal, epithelial-type polarity with electron-dense tight junctions, apical microvilli, and asymmetric distribution of organelles. Consistent with these findings, molecules that are components of tight junctions or play regulatory roles in polarization localized to the apical regions of the hESCs at sites of cell-cell contact. The tight junctions were functional, as shown by the ability of hESC colonies to exclude the pericellular passage of a biotin compound. Depolarization of hESCs produced multilayered aggregates of rapidly proliferating cells that continued to express transcription factors that are required for pluripotency at the same level as control cells. However, during embryoid body formation, depolarized cells differentiated predominantly along mesenchymal lineage and spontaneously produced hematoendothelial precursors more efficiently than control ESC. Our findings have numerous implications with regard to strategies for deriving, propagating, and differentiating hESC.

    Disruption of apical-basal polarity of human embryonic stem cells enhances hematoendothelial differentiation. Publishing Authors By Initials

    a krtolicaA Krtolica,o genbacevO Genbacev,c escobedoC Escobedo,t zdravkovicT Zdravkovic,a nordstromA Nordstrom,d vabuenaD Vabuena,a nathA Nath,c simonC Simon,k mostovK Mostov,sj fisherSJ Fisher,

    For similar carbohydrates: polysaccharides: proteoglycans research abstracts see: carbohydrates: polysaccharides: proteoglycans research

    PUBMED ID PMID:

    MEDLINE DATE:

    Disruption of apical-basal polarity of human embryonic stem cells enhances hematoendothelial differentiation. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Stem cells (Dayton, Ohio)

    VOLUME: 25

    Page Numbers: 2215-23

    Journal Abbreviation: Stem Cells

    ISSN: 1549-4918

    DAY: 14

    MONTH: 06

    YEAR: 2007

    Disruption of apical-basal polarity of human embryonic stem cells enhances hematoendothelial differentiation. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9304532

    Disruption of apical-basal polarity of human embryonic stem cells enhances hematoendothelial differentiation. Keywords Mesh Terms:

    KEYWORDS: Proteoglycans

    MESH TERMS: pharmacology

    Chemical & Substance for Abstract: Disruption of apical-basal polarity of human embryonic stem cells enhances hematoendothelial differentiation. Information

    Substance Name: Collagen

    Registry Number: 9007-34-5

    Grant and Affiliation Information for Disruption of apical-basal polarity of human embryonic stem cells enhances hematoendothelial differentiation.

    AFFILIATION: Department of Pharmaceutical Chemistry, University of California San Francisco, San Francisco, California 94143, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    GRANT:

    ACRONYM:

    MEDLINETA: Stem Cells

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