Publications by authors named "Steve Hildebrandt"

Neural stem/progenitor cells (NSPCs) have the potential to self-renew and to generate all neural lineages as well as to repopulate damaged areas in the brain. Our previous targeting strategies have indicated precursor cell heterogeneity between different brain regions that warrants the development of NSPC-specific delivery vehicles. Here, we demonstrate a target-specific adenoviral vector system for the in vivo manipulation of progenitor cells in the subventricular zone of the adult mouse brain.

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Background: Cardiac arrest (CA) followed by cardiopulmonary resuscitation (CPR) is associated with poor survival rate and neurofunctional outcome. Toll-like receptor 2 (TLR2) plays an important role in conditions of sterile inflammation such as reperfusion injury. Recent data demonstrated beneficial effects of the administration of TLR2-blocking antibodies in ischemia/reperfusion injury.

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Adult hippocampal neural stem cells (NSC) are an intriguing source for cell replacement or could serve as delivery vehicles for therapeutic genes. We recently reported selective transduction of adult mouse NSC in the DG by in vivo injection of GFP encoding adenoviral (Ad) vectors engineered to bind NSC-specific peptides. Here, we investigated the specificity of these peptide-tagged vectors in the adult rat DG, and whether they can be used to follow differentiation of infected cells over time.

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Article Synopsis
  • Neural precursor cells (NPC) in the adult brain are drawn to damaged areas, suggesting they could be harnessed for targeted therapy in conditions like cancer and neurodegeneration.
  • Researchers have identified specific ligands that can help target these NPCs for gene therapy via adenovirus, indicating a new method to enhance the delivery of therapeutic genes directly to affected brain regions.
  • This innovative approach opens up potential for improved restorative cell therapies and the ability to manipulate NPCs more effectively within the adult central nervous system.
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