Literature DB >> 2387238

Pathways of trunk neural crest cell migration in the mouse embryo as revealed by vital dye labelling.

G N Serbedzija1, S E Fraser, M Bronner-Fraser.   

Abstract

Analysis of neural crest cell migration in the mouse has been difficult due to the lack of reliable cell markers. Recently, we found that injection of DiI into the chick neural tube marks premigratory neural crest cells whose endfeet are in contact with the lumen of the neural tube (Serbedzija et al. Development 106, 809-819 (1989)). In the present study, this technique was applied to study neural crest cell migratory pathways in the trunk of the mouse embryo. Embryos were removed from the mother between the 8th and the 10th days of development and DiI was injected into the lumen of the neural tube. The embryos were then cultured for 12 to 24 h, and analyzed at the level of the forelimb. We observed two predominant pathways of neural crest cell migration: (1) a ventral pathway through the rostral portion of the somite and (2) a dorsolateral pathway between the dermamyotome and the epidermis. Neural crest cells were observed along the dorsolateral pathway throughout the period of migration. The distribution of labelled cells along the ventral pathway suggested that there were two overlapping phases of migration. An early ventrolateral phase began before E9 and ended by E9.5; this pathway consisted of a stream of cells within the rostral sclerotome, adjacent to the dermamyotome, that extended ventrally to the region of the sympathetic ganglia and the dorsal aorta.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1990        PMID: 2387238     DOI: 10.1242/dev.108.4.605

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  67 in total

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8.  Late-emigrating neural crest cells in the roof plate are restricted to a sensory fate by GDF7.

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9.  A segmented pattern of cell death during development of the chick embryo.

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Journal:  Anat Embryol (Berl)       Date:  1992

10.  Fate mapping of neural crest cells during eye development using a protein 0 promoter-driven transgenic technique.

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