Document Detail

Inductive differentiation of two neural lineages reconstituted in a microculture system from Xenopus early gastrula cells.
MedLine Citation:
PMID:  1769329     Owner:  NLM     Status:  MEDLINE    
Neural induction of ectoderm cells has been reconstituted and examined in a microculture system derived from dissociated early gastrula cells of Xenopus laevis. We have used monoclonal antibodies as specific markers to monitor cellular differentiation from three distinct ectoderm lineages in culture (N1 for CNS neurons from neural tube, Me1 for melanophores from neural crest and E3 for skin epidermal cells from epidermal lineages). CNS neurons and melanophores differentiate when deep layer cells of the ventral ectoderm (VE, prospective epidermis region; 150 cells/culture) and an appropriate region of the marginal zone (MZ, prospective mesoderm region; 5-150 cells/culture) are co-cultured, but not in cultures of either cell type on their own; VE cells cultured alone yield epidermal cells as we have previously reported. The extent of inductive neural differentiation in the co-culture system strongly depends on the origin and number of MZ cells initially added to culture wells. The potency to induce CNS neurons is highest for dorsal MZ cells and sharply decreases as more ventrally located cells are used. The same dorsoventral distribution of potency is seen in the ability of MZ cells to inhibit epidermal differentiation. In contrast, the ability of MZ cells to induce melanophores shows the reverse polarity, ventral to dorsal. These data indicate that separate developmental mechanisms are used for the induction of neural tube and neural crest lineages. Co-differentiation of CNS neurons or melanophores with epidermal cells can be obtained in a single well of co-cultures of VE cells (150) and a wide range of numbers of MZ cells (5 to 100). Further, reproducible differentiation of both neural lineages requires intimate association between cells from the two gastrula regions; virtually no differentiation is obtained when cells from the VE and MZ are separated in a culture well. These results indicate that the inducing signals from MZ cells for both neural tube and neural crest lineages affect only nearby ectoderm cells.
S Mitani; H Okamoto
Related Documents :
8275859 - Even-numbered rhombomeres control the apoptotic elimination of neural crest cells from ...
15917469 - Isolation and characterization of multipotent skin-derived precursors from human skin.
10851129 - In ovo time-lapse analysis after dorsal neural tube ablation shows rerouting of chick h...
7620899 - Müller cell survival and proliferation in response to medium conditioned by the retina...
5123259 - Neural crest origin of the endocrine polypeptide (apud) cells of the gastrointestinal t...
11262869 - Neuronal specification in the spinal cord: inductive signals and transcriptional codes.
11845329 - Bovine trophoblastic cell differentiation on collagen substrata: formation of binucleat...
7712479 - Alterations in the topoisomerase ii alpha gene, messenger rna, and subcellular protein ...
24142249 - A replication-inhibited unsegregated nucleoid at mid-cell blocks z-ring formation and c...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Development (Cambridge, England)     Volume:  112     ISSN:  0950-1991     ISO Abbreviation:  Development     Publication Date:  1991 May 
Date Detail:
Created Date:  1992-02-25     Completed Date:  1992-02-25     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  8701744     Medline TA:  Development     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  21-31     Citation Subset:  IM    
Department of Neurobiology, Faculty of Medicine, University of Tokyo, Japan.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Cell Differentiation / physiology
Cells, Cultured
Central Nervous System / embryology*
Cytological Techniques
Ectoderm / physiology*
Epidermis / embryology,  ultrastructure
Microscopy, Fluorescence
Microscopy, Phase-Contrast
Neural Crest / embryology,  ultrastructure
Xenopus laevis

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Integrin expression during human epidermal development in vivo and in vitro.
Next Document:  Formation and regeneration of rhombomere boundaries in the developing chick hindbrain.