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Protein components and signalling events regulating the lineage restriction of embryonic stem cells to neural stem cells

ReferenceC15291
Principal Investigator / Supervisor Dr Jane Wakeman
Co-Investigators /
Co-Supervisors
Institution Bangor University
DepartmentSch of Biological Sciences
Funding typeResearch
Value (£) 192,984
StatusCompleted
TypeResearch Grant
Start date 01/09/2001
End date 01/09/2004
Duration36 months

Abstract

Following gastrulation, pluripotent stem cells derived from the inner cell mass of the blastocyst, segregate into the three germ layers. From here, it has been assumed that their potential becomes more restricted as they mature and form tissue and organ specific stem cells. Molecular mechanisms and signalling components regulating this restriction in potency have not been addressed. We will take a proteomic approach to define components involved in signalling the restriction in potency as embryonic stem cells form neural stem cells. We will use the mouse ES cell model, enabling future studies to address function of identified components, and specific components. Definition of components is critical to decipher both mechanisms of tissue specific stem cell generation, and de-differentiation, which may govern a stem cells ability to demonstrate plasticity.

Summary

unavailable
Committee Closed Committee - Biochemistry & Cell Biology (BCB)
Research TopicsX – not assigned to a current Research Topic
Research PriorityX – Research Priority information not available
Research Initiative X - not in an Initiative
Funding SchemeX – not Funded via a specific Funding Scheme
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