Onset of neuronal differentiation is regulated by paraxial mesoderm and requires attenuation of FGF signalling

Development ◽  
2002 ◽  
Vol 129 (7) ◽  
pp. 1681-1691 ◽  
Author(s):  
Ruth Diez del Corral ◽  
Dorette N. Breitkreuz ◽  
Kate G. Storey

While many neuronal differentiation genes have been identified, we know little about what determines when and where neurons will form and how this process is coordinated with the differentiation of neighbouring tissues. In most vertebrates the onset of neuronal differentiation takes place in the spinal cord in a head to tail sequence. Here we demonstrate that the changing signalling properties of the adjacent paraxial mesoderm control the progression of neurogenesis in the chick spinal cord. We find an inverse relationship between the expression of caudal neural genes in the prospective spinal cord, which is maintained by underlying presomitic mesoderm and FGF signalling, and neuronal differentiation, which is repressed by such signals and accelerated by somitic mesoderm. We show that key to this interaction is the ability of somitic mesoderm to repress Fgf8 transcription in the prospective spinal cord. Our findings further indicate that attenuation of FGF signalling in the prospective spinal cord is a prerequisite for the onset of neuronal differentiation and may also help to resolve mesodermal and neural cell fates. However, inhibition of FGF signalling alone does not promote the formation of neurons, which requires still further somite signalling. We propose a model in which signalling from somitic tissue promotes the differentiation of the spinal cord and serves to co-ordinate neural and mesodermal development.

2021 ◽  
Author(s):  
Taiki Katsuyama ◽  
Minori Kadoya ◽  
Manabu Shirai ◽  
Noriaki Sasai

2006 ◽  
Vol 21 (1) ◽  
pp. 194-205 ◽  
Author(s):  
Ghanashyam D. Ghadge ◽  
Lijun Wang ◽  
Kamal Sharma ◽  
Anna Liza Monti ◽  
Vytas Bindokas ◽  
...  

1991 ◽  
Vol 132 (2) ◽  
pp. 155-158 ◽  
Author(s):  
Nobuo Okado ◽  
Mutsumi Matsukawa ◽  
Shinobu Noritake ◽  
Shigeru Ozaki ◽  
Shun Hamada ◽  
...  

Development ◽  
1982 ◽  
Vol 71 (1) ◽  
pp. 83-95
Author(s):  
L. Hsu ◽  
D. Natyzak ◽  
G. L. Trupin

Soluble fractions of homogenized skeletal muscle were found to promote neuronal migration and neuritic and glial outgrowth from embryonic chick spinal cord explants. Fractions obtained from skeletal muscle immobilized by prolonged treatment with curare were significantly more effective than normal muscle in accelerating neuronal and glial development. Fractions from other tissues such as brain and lung did not enhance neuronal differentiation, but were effective in stimulating outgrowth of glial cells. Separate measurements of glial and neuronal responses indicate that tissue fractions produce independent effects on the glial and neuronal components.


2006 ◽  
Vol 25 (15) ◽  
pp. 3664-3674 ◽  
Author(s):  
Mirit Snir ◽  
Rachel Ofir ◽  
Sarah Elias ◽  
Dale Frank

2006 ◽  
Vol 17 (5) ◽  
pp. 2278-2286 ◽  
Author(s):  
Darya Kiryushko ◽  
Irina Korshunova ◽  
Vladimir Berezin ◽  
Elisabeth Bock

The neural cell adhesion molecule (NCAM) plays a pivotal role in the development of the nervous system, promoting neuronal differentiation via homophilic (NCAM–NCAM) as well as heterophilic (NCAM-fibroblast growth factor receptor [FGFR]) interactions. NCAM-induced intracellular signaling has been shown to affect and be dependent on the cytoplasmic Ca2+ concentration ([Ca2+]i). However, the molecular basis of this remains unclear. In this study, we determined [Ca2+]i regulating mechanisms involved in intracellular signaling induced by NCAM. To mimic the effect of homophilic NCAM interaction on [Ca2+]i in vitro, we used a peptide derived from a homophilic binding site of NCAM, termed P2, which triggers signaling cascades similar to those activated by NCAM–NCAM interaction. We found that P2 increased [Ca2+]i in primary hippocampal neurons. This effect depended on two signaling pathways. The first pathway was associated with activation of FGFR, phospholipase Cγ, and production of diacylglycerol, and the second pathway involved Src-family kinases. Moreover, NCAM-mediated Ca2+ entry required activation of nonselective cation and T-type voltage-gated Ca2+ channels. These channels, together with the Src-family kinases, were also involved in neuritogenesis induced by physiological, homophilic NCAM interactions. Thus, unanticipated mechanisms of Ca2+ homeostasis are shown to be activated by NCAM and to contribute to neuronal differentiation.


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