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Stem Cell Reports ; 3(5): 774-88, 2014 Nov 11.
Article in English | MEDLINE | ID: mdl-25418723

ABSTRACT

Resident neural precursor cells (NPCs) have been reported for a number of adult tissues. Understanding their physiological function or, alternatively, their activation after tissue damage or in vitro manipulation remains an unsolved issue. Here, we investigated the source of human dermal NPCs in adult tissue. By following an unbiased, comprehensive approach employing cell-surface marker screening, cell separation, transcriptomic characterization, and in vivo fate analyses, we found that p75NTR(+) precursors of human foreskin can be ascribed to the Schwann (CD56(+)) and perivascular (CD56(-)) cell lineages. Moreover, neural differentiation potential was restricted to the p75NTR(+)CD56(+) Schwann cells and mediated by SOX2 expression levels. Double-positive NPCs were similarly obtained from human cardiospheres, indicating that this phenomenon might be widespread.


Subject(s)
Cell Lineage , Dermis/cytology , Neural Stem Cells/cytology , Schwann Cells/cytology , Adolescent , Adult , Aged , Animals , CD56 Antigen/genetics , CD56 Antigen/metabolism , Cell Differentiation/genetics , Cells, Cultured , Child , Child, Preschool , Dermis/metabolism , Foreskin/cytology , Gene Expression Profiling , Humans , Infant , Male , Mice , Microscopy, Confocal , Middle Aged , Nerve Tissue Proteins/genetics , Nerve Tissue Proteins/metabolism , Neural Stem Cells/metabolism , Neurons/cytology , Neurons/metabolism , Receptors, Nerve Growth Factor/genetics , Receptors, Nerve Growth Factor/metabolism , Reverse Transcriptase Polymerase Chain Reaction , Schwann Cells/metabolism , Young Adult
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