Artigo Acesso aberto Revisado por pares

Gene Transfer of an Engineered Transcription Factor Promoting Expression of VEGF-A Protects Against Experimental Diabetic Neuropathy

2006; American Diabetes Association; Volume: 55; Issue: 6 Linguagem: Inglês

10.2337/db05-1060

ISSN

1939-327X

Autores

Sally Price, Carolyn L. Dent, Beatriz Duran-Jimenez, Yuxin Liang, Lei Zhang, Edward J. Rebar, Casey C. Case, Philip D. Gregory, Tyler J. Martin, S. Kaye Spratt, David R. Tomlinson,

Tópico(s)

Signaling Pathways in Disease

Resumo

Peripheral neuropathy is a common, irreversible complication of diabetes. We investigated whether gene transfer of an engineered zinc finger protein transcription factor (ZFP-TF) designed to upregulate expression of the endogenous vascular endothelial growth factor (VEGF)-A gene could protect against experimental diabetic neuropathy. ZFP-TF–driven activation of the endogenous gene results in expression of all of the VEGF-A isoforms, a fact that may be of significance for recapitulation of the proper biological responses stimulated by this potent neuroprotective growth factor. We show here that this engineered ZFP-TF activates VEGF-A in appropriate cells in culture and that the secreted VEGF-A protein induced by the ZFP protects neuroblastoma cell lines from a serum starvation insult in vitro. Importantly, single and repeat intramuscular injections of formulated plasmid DNA encoding the VEGF-A–activating ZFP-TF resulted in protection of both sensory and motor nerve conduction velocities in a streptozotocin-induced rat model of diabetes. These data suggest that VEGF-A–activating ZFP-TFs may ultimately be of clinical utility in the treatment of this disease.

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