IMR Press / FBL / Volume 11 / Issue 3 / DOI: 10.2741/2042

Frontiers in Bioscience-Landmark (FBL) is published by IMR Press from Volume 26 Issue 5 (2021). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on imrpress.com as a courtesy and upon agreement with Frontiers in Bioscience.

Article

Recombinant adeno-associated viral vector encoding human VEGF165 induces neomicrovessel formation in the adult mouse brain

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1 Center for Cerebrovascular Research, Department of Anesthesia and Perioperative Care, University of California, San Francisco, CA 94110, USA
2 Departments of Laboratory Medicine, University of California, San Francisco, San Francisco, CA 94110
3 Departments of Neurological Surgery, University of California, San Francisco, San Francisco, CA 94110
4 Departments of Neurology, University of California, San Francisco, San Francisco, CA 94110
5 Department of Neurology, Ruijin Hospital, Shanghai Second Medical University, Shanghai 200025, China
Front. Biosci. (Landmark Ed) 2006, 11(3), 3190–3198; https://doi.org/10.2741/2042
Published: 1 September 2006
Abstract

Delivery of therapeutic genes represents a fascinating possibility to accelerate the injury-repairing process in tissues that are otherwise difficult to treat, such as cerebral ischemia. Current studies indicate that gene transfer-induced focal angiogenesis in the brain may provide an important therapeutic strategy. In the present study, we report the efficacy of induction of angiogenesis with an adeno-associated virus (AAV) vector expressing the 165 amino acid isoform of vascular endothelial growth factor (VEGF165). We found that AAV serotype 1 had more efficiency in transduction of the brain tissue than AAV serotype 2. Quantitative vessel counting showed that microvessels in AAV-VEGF-transduced mice significantly increased from 1 to 12 weeks compared to the control groups (AAV-VEGF: 316±58 vs. AAV-lacZ: 180±34 and saline: 152±35 vessels/mm2, at 6 weeks, p<0.05). Proliferating cell nuclear antigen (PCNA) staining confirmed these microvessels were actively proliferating. Double-labeled fluorescence staining demonstrated that neurons, astrocytes, and endothelial cells could express VEGF following AAV-VEGF gene transfer. AAV vectors did not elicit a detectable inflammatory response, cell loss or neuronal damage. Our data underline the importance of angiogenesis in the brain tissue and indicate that VEGF gene transfer may present a valuable approach to treat brain ischemic disorders.

Keywords
Adeno-associated viral vector
Angiogenesis
Brain
Gene transfer
VEGF
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