Literature DB >> 18804450

Derivation of cranial neural crest-like cells from human embryonic stem cells.

Yan Zhou1, Malcolm L Snead.   

Abstract

The neural crest is a transient population of multipotent progenitors contributing to a diverse array of tissues throughout the vertebrate embryo. Embryonic stem (ES) cells are able to form embryoid body and spontaneously differentiate to various lineages, following a reproducible temporal pattern of development that recapitulates early embryogenesis. Embryoid bodies were triturated and the dissociated cells were processed for fluorescence-activated cell sorting (FACS), and more than 1% of cells were identified as frizzled-3(+)/cadherin-11(+). Expression of marker genes associated with various terminal fates was detected for chondrocytes, glia, neurons, osteoblasts and smooth muscles, indicating that the FACS-sorted frizzled-3(+)/cadherin-11(+) cells were multipotent progenitor cells capable of differentiating to fates associated with cranial neural crest. Moreover, the sorted cells were able to self-renew and maintain multipotent differentiation potential. The derivation of cranial neural crest-like multipotent progenitor cells from ES cells provides a new tool for cell lineage analysis of neural crest in vitro.

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Year:  2008        PMID: 18804450      PMCID: PMC2574922          DOI: 10.1016/j.bbrc.2008.09.032

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  40 in total

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Journal:  Stem Cells       Date:  2006-03-30       Impact factor: 6.277

3.  Xenopus cadherin-11 is expressed in different populations of migrating neural crest cells.

Authors:  J Vallin; J M Girault; J P Thiery; F Broders
Journal:  Mech Dev       Date:  1998-07       Impact factor: 1.882

4.  Control of neural crest cell fate by the Wnt signalling pathway.

Authors:  R I Dorsky; R T Moon; D W Raible
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5.  Generation of peripheral sensory and sympathetic neurons and neural crest cells from human embryonic stem cells.

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6.  Differential expression of the Wnt putative receptors Frizzled during mouse somitogenesis.

Authors:  U Borello; V Buffa; C Sonnino; R Melchionna; E Vivarelli; G Cossu
Journal:  Mech Dev       Date:  1999-12       Impact factor: 1.882

7.  Xenopus cadherin-11 (Xcadherin-11) expression requires the Wg/Wnt signal.

Authors:  B Hadeball; A Borchers; D Wedlich
Journal:  Mech Dev       Date:  1998-03       Impact factor: 1.882

8.  Isolation and directed differentiation of neural crest stem cells derived from human embryonic stem cells.

Authors:  Gabsang Lee; Hyesoo Kim; Yechiel Elkabetz; George Al Shamy; Georgia Panagiotakos; Tiziano Barberi; Viviane Tabar; Lorenz Studer
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9.  Odontogenic epithelium induces similar molecular responses in chick and mouse mandibular mesenchyme.

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  18 in total

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Journal:  Cell Res       Date:  2012-01-10       Impact factor: 25.617

3.  Wnt signaling and a Smad pathway blockade direct the differentiation of human pluripotent stem cells to multipotent neural crest cells.

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Review 4.  Pluripotent stem cells for Schwann cell engineering.

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Journal:  Stem Cell Rev Rep       Date:  2015-04       Impact factor: 5.739

5.  Derivation of neural crest cells from human pluripotent stem cells.

Authors:  Gabsang Lee; Stuart M Chambers; Mark J Tomishima; Lorenz Studer
Journal:  Nat Protoc       Date:  2010-03-18       Impact factor: 13.491

6.  Quantitative Multimodal Evaluation of Passaging Human Neural Crest Stem Cells for Peripheral Nerve Regeneration.

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7.  Notch1 signaling regulates chondrogenic lineage determination through Sox9 activation.

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8.  Human neural crest stem cells derived from human ESCs and induced pluripotent stem cells: induction, maintenance, and differentiation into functional schwann cells.

Authors:  Qiuyue Liu; Steven C Spusta; Ruifa Mi; Rhonda N T Lassiter; Michael R Stark; Ahmet Höke; Mahendra S Rao; Xianmin Zeng
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Review 9.  Current perspectives of the signaling pathways directing neural crest induction.

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10.  Derivation of corneal endothelial cell-like cells from rat neural crest cells in vitro.

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Journal:  PLoS One       Date:  2012-07-31       Impact factor: 3.240

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