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Systemic biopolymer-delivered vascular endothelial growth factor promotes therapeutic angiogenesis in experimental renovascular disease.
Chade, Alejandro R; Williams, Maxx L; Guise, Erika; Vincent, Luke J; Harvey, Taylor W; Kuna, Marija; Mahdi, Fakhri; Bidwell, Gene L.
Afiliação
  • Chade AR; Department of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, Mississippi, USA; Department of Medicine, University of Mississippi Medical Center, Jackson, Mississippi, USA; Department of Radiology, University of Mississippi Medical Center, Jackson, Mississippi, USA. Ele
  • Williams ML; Department of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, Mississippi, USA.
  • Guise E; Department of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, Mississippi, USA.
  • Vincent LJ; Department of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, Mississippi, USA.
  • Harvey TW; Department of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, Mississippi, USA.
  • Kuna M; Department of Biochemistry, University of Mississippi Medical Center, Jackson, Mississippi, USA.
  • Mahdi F; Department of Neurology, University of Mississippi Medical Center, Jackson, Mississippi, USA.
  • Bidwell GL; Department of Biochemistry, University of Mississippi Medical Center, Jackson, Mississippi, USA; Department of Neurology, University of Mississippi Medical Center, Jackson, Mississippi, USA.
Kidney Int ; 93(4): 842-854, 2018 04.
Article em En | MEDLINE | ID: mdl-29273331
ABSTRACT
We recently developed a therapeutic biopolymer composed of an elastin-like polypeptide (ELP) fused to vascular endothelial growth factor (VEGF) and showed long-term renoprotective effects in experimental renovascular disease after a single intra-renal administration. Here, we sought to determine the specificity, safety, efficacy, and mechanisms of renoprotection of ELP-VEGF after systemic therapy in renovascular disease. We tested whether kidney selectivity of the ELP carrier would reduce off-target binding of VEGF in other organs. In vivo bio-distribution after systemic administration of ELP-VEGF in swine was determined in kidneys, liver, spleen, and heart. Stenotic-kidney renal blood flow and glomerular filtration rate were quantified in vivo using multi-detector computed tomography (CT) after six weeks of renovascular disease, then treated with a single intravenous dose of ELP-VEGF or placebo and observed for four weeks. CT studies were then repeated and the pigs euthanized. Ex vivo studies quantified renal microvascular density (micro-CT) and fibrosis. Kidneys, liver, spleen, and heart were excised to quantify the expression of angiogenic mediators and markers of progenitor cells. ELP-VEGF accumulated predominantly in the kidney and stimulated renal blood flow, glomerular filtration rate, improved cortical microvascular density, and renal fibrosis, and was accompanied by enhanced renal expression of VEGF, downstream mediators of VEGF signaling, and markers of progenitor cells compared to placebo. Expression of angiogenic factors in liver, spleen, and heart were not different compared to placebo-control. Thus, ELP efficiently directs VEGF to the kidney after systemic administration and induces long-term renoprotection without off-target effects, supporting the feasibility and safety of renal therapeutic angiogenesis via systemic administration of a novel kidney-specific bioengineered compound.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peptídeos / Obstrução da Artéria Renal / Neovascularização Fisiológica / Fator A de Crescimento do Endotélio Vascular / Indutores da Angiogênese / Rim Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Kidney Int Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peptídeos / Obstrução da Artéria Renal / Neovascularização Fisiológica / Fator A de Crescimento do Endotélio Vascular / Indutores da Angiogênese / Rim Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Kidney Int Ano de publicação: 2018 Tipo de documento: Article