Literature DB >> 29427146

From the primitive streak to the somitic mesoderm: labeling the early stages of chick embryos using EGFP transfection.

Haiming Fan1, Nobuyuki Sakamoto1, Hirohiko Aoyama2.   

Abstract

Mesoderm is derived from the primitive streak. The rostral region of the primitive streak forms the somitic mesoderm. We have previously shown the developmental origin of each level of the somitic mesoderm using DiI fluorescence labeling of the primitive streak. We found that the more caudal segments were derived from the primitive streak during the later developmental stages. DiI labeled several pairs of somites and showed the distinct rostral boundary; however, the fluorescence gradually disappeared in the caudal region. This finding can be explained in two ways: the primitive streak at a specific developmental stage is primordial of only a certain number of pairs of somites, or the DiI fluorescent dye was gradually diluted within the primitive streak by cell division. Here, we traced the development of the primitive streak cells using enhanced green fluorescent protein (EGFP) transfection. We confirmed that, the later the EGFP transfection stage, the more caudal the somites labeled. Different from DiI labeling, EGFP transfection performed at any developmental stage labeled the entire somitic mesoderm from the anterior boundary to the tail bud in 4.5-day-old embryos. Furthermore, the secondary neural tube was also labeled, suggesting that not only the somite precursor cells but also the axial stem cells were labeled.

Entities:  

Keywords:  Chick; Developmental fate; In ovo electroporation; Primitive streak; Somite

Mesh:

Substances:

Year:  2018        PMID: 29427146     DOI: 10.1007/s12565-018-0429-y

Source DB:  PubMed          Journal:  Anat Sci Int        ISSN: 1447-073X            Impact factor:   1.741


  19 in total

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Authors:  J M Brown; K G Storey
Journal:  Curr Biol       Date:  2000-07-13       Impact factor: 10.834

Review 2.  Axial stem cells deriving both posterior neural and mesodermal tissues during gastrulation.

Authors:  Hisato Kondoh; Tatsuya Takemoto
Journal:  Curr Opin Genet Dev       Date:  2012-05-09       Impact factor: 5.578

3.  Regulation of cell migration during chick gastrulation.

Authors:  Manli Chuai; Cornelis Jan Weijer
Journal:  Curr Opin Genet Dev       Date:  2009-07-31       Impact factor: 5.578

4.  The lunatic fringe gene is a target of the molecular clock linked to somite segmentation in avian embryos.

Authors:  M J McGrew; J K Dale; S Fraboulet; O Pourquié
Journal:  Curr Biol       Date:  1998-08-27       Impact factor: 10.834

5.  A series of normal stages in the development of the chick embryo.

Authors:  V HAMBURGER; H L HAMILTON
Journal:  J Morphol       Date:  1951-01       Impact factor: 1.804

6.  Primitive-streak origin of the cardiovascular system in avian embryos.

Authors:  V Garcia-Martinez; G C Schoenwolf
Journal:  Dev Biol       Date:  1993-10       Impact factor: 3.582

7.  Efficient targeting of gene expression in chick embryos by microelectroporation.

Authors:  T Momose; A Tonegawa; J Takeuchi; H Ogawa; K Umesono; K Yasuda
Journal:  Dev Growth Differ       Date:  1999-06       Impact factor: 2.053

Review 8.  Genetic control of caudal development.

Authors:  M Catala
Journal:  Clin Genet       Date:  2002-02       Impact factor: 4.438

9.  A spinal cord fate map in the avian embryo: while regressing, Hensen's node lays down the notochord and floor plate thus joining the spinal cord lateral walls.

Authors:  M Catala; M A Teillet; E M De Robertis; M L Le Douarin
Journal:  Development       Date:  1996-09       Impact factor: 6.868

10.  A fate map of the epiblast of the early chick embryo.

Authors:  Y Hatada; C D Stern
Journal:  Development       Date:  1994-10       Impact factor: 6.868

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  2 in total

1.  Double-layered two-directional somatopleural cell migration during chicken body wall development revealed with local fluorescent tissue labeling.

Authors:  Nobuyuki Sakamoto; Hirohiko Aoyama; Koji Ikegami
Journal:  Anat Sci Int       Date:  2022-02-20       Impact factor: 1.693

2.  Early activating somatic PIK3CA mutations promote ectopic muscle development and upper limb overgrowth.

Authors:  Sofia Frisk; Fulya Taylan; Izabela Blaszczyk; Inger Nennesmo; Göran Annerén; Bettina Herm; Eva-Lena Stattin; Vasilios Zachariadis; Anna Lindstrand; Bianca Tesi; Tobias Laurell; Ann Nordgren
Journal:  Clin Genet       Date:  2019-05-09       Impact factor: 4.438

  2 in total

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