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1.
Dev Dyn ; 236(2): 389-403, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17183528

ABSTRACT

Using cell markers and grafting, we examined the timing of migration and developmental potential of trunk neural crest cells in axolotl. No obvious differences in pathway choice were noted for DiI-labeling at different lateral or medial positions of the trunk neural folds in neurulae, which contributed not only to neural crest but also to Rohon-Beard neurons. Labeling wild-type dorsal trunks at pre- and early-migratory stages revealed that individual neural crest cells migrate away from the neural tube along two main routes: first, dorsolaterally between the epidermis and somites and, later, ventromedially between the somites and neural tube/notochord. Dorsolaterally migrating crest primarily forms pigment cells, with those from anterior (but not mid or posterior) trunk neural folds also contributing glia and neurons to the lateral line. White mutants have impaired dorsolateral but normal ventromedial migration. At late migratory stages, most labeled cells move along the ventromedial pathway or into the dorsal fin. Contrasting with other anamniotes, axolotl has a minor neural crest contribution to the dorsal fin, most of which arises from the dermomyotome. Taken together, the results reveal stereotypic migration and differentiation of neural crest cells in axolotl that differ from other vertebrates in timing of entry onto the dorsolateral pathway and extent of contribution to some derivatives.


Subject(s)
Ambystoma/embryology , Cell Differentiation/physiology , Cell Movement/physiology , Neural Crest/embryology , Animals , Carbocyanines , Fluorescent Dyes , Image Processing, Computer-Assisted , Immunohistochemistry , In Situ Hybridization , Microscopy, Confocal , Microscopy, Fluorescence , Neural Crest/cytology
2.
Gene Expr Patterns ; 3(4): 455-8, 2003 Aug.
Article in English | MEDLINE | ID: mdl-12915311

ABSTRACT

The transcription factor Ets-1 is expressed in many different migratory cell types, suggesting that it may play an important role in regulating motility. To determine whether its expression in the neural crest is consistent with such a function, we have performed a detailed analysis of its expression during early chick embryogenesis. Our results show that this transcription factor is up-regulated in the cranial neural folds and dorsal neural tube approximately 4-6 h prior to commencement of neural crest migration. c-Ets-1 continues to be expressed by migrating cranial neural crest cells and subsequently by some neural crest-derived tissues. In addition to neural crest, we find expression of c-Ets-1 in endothelial cells of blood vessels, in somitic and intermediate mesoderm, in limb buds and in the heart.


Subject(s)
Cell Movement/physiology , Embryonic and Fetal Development , Gene Expression Regulation, Developmental , Neural Crest/blood supply , Neural Crest/embryology , Proto-Oncogene Proteins/metabolism , Transcription Factors/metabolism , Animals , Chick Embryo , Chickens , Cranial Nerves/blood supply , Cranial Nerves/cytology , Cranial Nerves/embryology , Proto-Oncogene Protein c-ets-1 , Proto-Oncogene Proteins c-ets
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