Literature DB >> 1936578

In vitro clonal analysis of quail cardiac neural crest development.

K Ito1, M Sieber-Blum.   

Abstract

The developmental potentials of cardiac neural crest cells were investigated by in vitro clonal analysis. Five morphologically distinct types of clones were observed: (1) "pigmented" clones contained melanocytes only; (2) "mixed" clones consisted of pigmented and unpigmented cells; (3) "unpigmented dense" clones consisted of flattened, closely aligned unpigmented cells; (4) "unpigmented loose" clones consisted of a few loosely arranged, flattened cells; and (5) "unpigmented large" clones included a large number of small, stellate cells that were highly proliferative. The binding patterns of antibodies against lineage-specific markers showed that cells in the different clones expressed characteristic phenotypes. The following phenotypes were expressed in addition to pigment cells: smooth muscle cells, connective tissue cells, chondrocytes, and cells in the sensory neuron lineage. Mixed clones expressed all five phenotypes. Unpigmented dense clones contained smooth muscle cells, connective tissue cells, chondrocytes, and sensory neurons. Unpigmented loose clones exclusively consisted of smooth muscle cells, whereas unpigmented large clones contained chondrocytes and sensory neuron precursors. Based on these results, the following conclusions can be drawn: (1) Pigmented and unpigmented loose clones are most likely formed by precursors that are committed to the melanogenic and myogenic cell lineages, respectively. (2) Mixed and unpigmented dense clones are derived from pluripotent cells with the capacity to give rise to four or five phenotypes. (3) Unpigmented large clones originate from progenitor cells that appear to have a partially restricted developmental potential, that is, these cells are capable of generating two phenotypes in clonal cultures. Thus, the data indicate that the early migratory cardiac neural crest is a heterogeneous population of cells, consisting of pluripotent cells, cells with a partially restricted developmental potential, and cells committed to a particular cell lineage.

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Year:  1991        PMID: 1936578     DOI: 10.1016/0012-1606(91)90320-3

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  17 in total

1.  Self-renewal capacity is a widespread property of various types of neural crest precursor cells.

Authors:  Andréa Trentin; Corinne Glavieux-Pardanaud; Nicole M Le Douarin; Elisabeth Dupin
Journal:  Proc Natl Acad Sci U S A       Date:  2004-03-15       Impact factor: 11.205

Review 2.  Regional differences in neural crest morphogenesis.

Authors:  Bryan R Kuo; Carol A Erickson
Journal:  Cell Adh Migr       Date:  2010 Oct-Dec       Impact factor: 3.405

3.  High frequency of cephalic neural crest cells shows coexistence of neurogenic, melanogenic, and osteogenic differentiation capacities.

Authors:  Giordano W Calloni; Nicole M Le Douarin; Elisabeth Dupin
Journal:  Proc Natl Acad Sci U S A       Date:  2009-05-15       Impact factor: 11.205

Review 4.  Review: the role of neural crest cells in the endocrine system.

Authors:  Meghan Sara Adams; Marianne Bronner-Fraser
Journal:  Endocr Pathol       Date:  2009       Impact factor: 3.943

5.  Sonic Hedgehog promotes the development of multipotent neural crest progenitors endowed with both mesenchymal and neural potentials.

Authors:  Giordano W Calloni; Corinne Glavieux-Pardanaud; Nicole M Le Douarin; Elisabeth Dupin
Journal:  Proc Natl Acad Sci U S A       Date:  2007-12-06       Impact factor: 11.205

6.  Vagal neural crest cell migratory behavior: a transition between the cranial and trunk crest.

Authors:  Bryan R Kuo; Carol A Erickson
Journal:  Dev Dyn       Date:  2011-09       Impact factor: 3.780

Review 7.  Molecular regulation of neural crest development.

Authors:  M Murphy; P F Bartlett
Journal:  Mol Neurobiol       Date:  1993       Impact factor: 5.590

8.  Neural crest stem cell multipotency requires Foxd3 to maintain neural potential and repress mesenchymal fates.

Authors:  Nathan A Mundell; Patricia A Labosky
Journal:  Development       Date:  2011-01-12       Impact factor: 6.868

Review 9.  Thyroid parafollicular cells. An accessible model for the study of serotonergic neurons.

Authors:  A F Russo; M S Clark; P L Durham
Journal:  Mol Neurobiol       Date:  1996-12       Impact factor: 5.590

Review 10.  Growth factor action in neural crest cell diversification.

Authors:  M Sieber-Blum; J M Zhang
Journal:  J Anat       Date:  1997-11       Impact factor: 2.610

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