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Generation of a Three-dimensional Full Thickness Skin Equivalent and Automated Wounding
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Neocortex patterning by the secreted signaling molecule FGF8.

T Fukuchi-Shimogori1, E A Grove

  • 1Department of Neurobiology, Pharmacology and Physiology, University of Chicago, Chicago, IL 60637, USA.

Science (New York, N.Y.)
|September 22, 2001
PubMed
Summary

Fibroblast growth factor 8 (FGF8) signaling regulates the development of the mammalian neocortical area map. Manipulating FGF8 levels or sources alters area boundaries and can cause duplications, revealing its role in specifying positional identity.

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Area of Science:

  • Neuroscience
  • Developmental Biology
  • Genetics

Background:

  • The mammalian neocortex is organized into distinct functional areas.
  • The molecular mechanisms driving the formation of this area map during neurogenesis remain largely unknown.

Purpose of the Study:

  • To investigate the role of Fibroblast Growth Factor 8 (FGF8) in the development of the neocortical area map.
  • To elucidate the molecular mechanisms underlying the specification of positional identity in the neocortex.

Main Methods:

  • Utilized electroporation-mediated gene transfer in mouse embryos.
  • Manipulated the endogenous anterior FGF8 signal by augmenting or reducing its levels.
  • Introduced an ectopic posterior source of FGF8.

Main Results:

  • Augmenting anterior FGF8 signal shifted neocortical area boundaries posteriorly.
  • Reducing anterior FGF8 signal shifted area boundaries anteriorly.
  • Ectopic posterior FGF8 source induced partial area duplications, evidenced by ectopic somatosensory barrel fields.

Conclusions:

  • FGF8 signaling, originating from the anterior telencephalon, is a key regulator of neocortical area map development.
  • FGF8 plays a critical role in specifying positional identity within the developing neocortex.