4.8 Article

The effect of encapsulated VEGF-secreting cells on brain amyloid load and behavioral impairment in a mouse model of Alzheimer's disease

Journal

BIOMATERIALS
Volume 31, Issue 21, Pages 5608-5618

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2010.03.042

Keywords

Angiogenesis; Animal model; Brain; Microencapsulation; Endothelial cells

Funding

  1. Fondo de Investigacion Sanitaria (FIS) [CP04/00179, PI060155]
  2. Comunidad de Madrid [2006.125]
  3. Ministerio de Ciencia e Innovacion [SAF2008-03157]

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Cerebrovascular dysfunction contributes to cognitive decline and neurodegeneration in Alzheimer's disease (AD). Vascular endothelial growth factor (VEGF), an angiogenic protein with important neurotrophic and neuroprotective actions, is under investigation as a therapeutic agent for the treatment of neurodegenerative disorders. The aim of this study was to generate encapsulated VEGF-secreting cells and implant them in a transgenic mouse model of AD, the double mutant amyloid precursor protein/presenilin 1 (APP/Ps1) mice, which shows a disturbed vessel homeostasis. We report that, after implantation of VEGF microcapsules, brain A beta burden, hyperphosphorylated-tau and cognitive impairment attenuated in APP/Ps1 mice. Based on the neurovascular hypothesis, our findings suggest a new potential therapeutic approach that could be developed for AD, to enhance A beta clearance and neurovascular repair, and to protect the cognitive behavior. Stereologically-implanted encapsulated VEGF-secreting cells could offer an alternative strategy in the treatment of AD. (c) 2010 Elsevier Ltd. All rights reserved.

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