The limited capability of the central nervous system (CNS) to repair itself after damage remains a significant challenge for basic and clinical sciences. Among the approaches for restoration of lost neuronal function, the use of embryonic stem (ES) cells as donor source for neural transplantation is increasingly receiving attention. Yet, there is a surprising shortage of data demonstrating functional characteristics of ES cell-derived progeny incorporating into damaged CNS circuitries. In recent studies, we have determined basic morphological and functional attributes of ES cell-derived astrocytes and neurons integrating into normal hippocampal tissue. In this grant application we propose the anatomical and functional evaluation of ES cell-derived neural precursors (ESNPs) grafted into the structurally impaired hippocampal formation. Although in vivo studies are planned for data confirmation, our experimental approach primarily involves transplantation and electrophysiological characterization of fluorescent-labeled ESNPs in organotypic hippocampal slice cultures (HSCs). HSCs will be derived from two animal models with severe neuronal cell loss affecting and impairing the hippocampal formation: the flathead mutant and sublethally irradiated Wistar rats. The rationale for choosing the animal models was that, although etiologically different, they both have in common a loss of a significant amount of neurons in the hippocampus. The flathead mutants are affected from severe impairments in the generation of dentate gyrus granule cells and interneurons, due to an inherited loss of the citron kinase gene. Wistar rats, which receive external brain irradiation in early postnatal life stages show a significant loss of granule cells, representing a somewhat acquired form of injury. As functional integration may depend on both, the environmental characteristics of the recipient CNS structure, and on the nature of engrafted cells, we will additionally explore the need of defining suitable donor cell populations for successful neural circuitry integration. The synaptic integration of ESNP-derived neurons and their functional interactions with disrupted or degenerated host circuitries may serve as a novel experimental platform for the development of neural transplantation strategies for a variety of neurological diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21NS046384-02
Application #
6845346
Study Section
National Institute of Neurological Disorders and Stroke Initial Review Group (NSD)
Program Officer
Owens, David F
Project Start
2004-02-01
Project End
2007-01-31
Budget Start
2005-02-01
Budget End
2007-01-31
Support Year
2
Fiscal Year
2005
Total Cost
$168,234
Indirect Cost
Name
University of Florida
Department
Neurosciences
Type
Schools of Medicine
DUNS #
969663814
City
Gainesville
State
FL
Country
United States
Zip Code
32611
Walton, Noah M; Snyder, Gregory E; Park, Donghyun et al. (2009) Gliotypic neural stem cells transiently adopt tumorigenic properties during normal differentiation. Stem Cells 27:280-9
Shepherd, Timothy M; Scheffler, Bjorn; King, Michael A et al. (2006) MR microscopy of rat hippocampal slice cultures: a novel model for studying cellular processes and chronic perturbations to tissue microstructure. Neuroimage 30:780-6