Literature DB >> 16319820

Intravitreous injection of PLGA microspheres encapsulating GDNF promotes the survival of photoreceptors in the rd1/rd1 mouse.

Charlotte Andrieu-Soler1, Anne Aubert-Pouëssel, Marc Doat, Serge Picaud, Mounia Halhal, Manuel Simonutti, Marie-Claire Venier-Julienne, Jean-Pierre Benoit, Francine Behar-Cohen.   

Abstract

PURPOSE: To evaluate the potential delay of the retinal degeneration in rd1/rd1 mice using recombinant human glial cell line-derived neurotrophic factor (rhGDNF) encapsulated in poly(D,L-lactide-co-glycolide) (PLGA) microspheres.
METHODS: rhGDNF-loaded PLGA microspheres were prepared using a water in oil in water (w/o/w) emulsion solvent extraction-evaporation process. In vitro, the rhGDNF release profile was assessed using radiolabeled factor. In vivo, rhGDNF microspheres, blank microspheres, or microspheres loaded with inactivated rhGDNF were injected into the vitreous of rd1/rd1 mice at postnatal day 11 (PN11). The extent of retinal degeneration was examined at PN28 using rhodopsin immunohistochemistry on whole flat-mount retinas, outer nuclear layer (ONL) cell counting on histology sections, and electroretinogram tracings. Immunohistochemical reactions for glial fibrillary acidic protein (GFAP), F4/80, and rhodopsin were performed on cryosections.
RESULTS: Significant delay of rod photoreceptors degeneration was observed in mice receiving the rhGDNF-loaded microspheres compared to either untreated mice or to mice receiving blank or inactivated rhGDNF microspheres. The degeneration delay in the eyes receiving the rhGDNF microspheres was illustrated by the increased rhodopsin positive signals, the preservation of significantly higher number of cell nuclei within the ONL, and significant b-wave increase. A reduction of the subretinal glial proliferation was also observed in these treated eyes. No significant intraocular inflammatory reaction was observed after the intravitreous injection of the various microspheres.
CONCLUSIONS: A single intravitreous injection of rhGDNF-loaded microspheres slows the retinal degeneration processes in rd1/rd1 mice. The use of injectable, biodegradable polymeric systems in the vitreous enables the efficient delivery of therapeutic proteins for the treatment of retinal diseases.

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Year:  2005        PMID: 16319820

Source DB:  PubMed          Journal:  Mol Vis        ISSN: 1090-0535            Impact factor:   2.367


  22 in total

1.  Controlled release of glial cell line-derived neurotrophic factor from poly(ε-caprolactone) microspheres.

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Journal:  Drug Deliv Transl Res       Date:  2014-04       Impact factor: 4.617

2.  Classical complement activation and acquired immune response pathways are not essential for retinal degeneration in the rd1 mouse.

Authors:  Bärbel Rohrer; Christina Demos; Rico Frigg; Christian Grimm
Journal:  Exp Eye Res       Date:  2006-10-25       Impact factor: 3.467

Review 3.  Pharmaceutical microscale and nanoscale approaches for efficient treatment of ocular diseases.

Authors:  I Bravo-Osuna; V Andrés-Guerrero; P Pastoriza Abal; I T Molina-Martínez; R Herrero-Vanrell
Journal:  Drug Deliv Transl Res       Date:  2016-12       Impact factor: 4.617

4.  Activated mTORC1 promotes long-term cone survival in retinitis pigmentosa mice.

Authors:  Aditya Venkatesh; Shan Ma; Yun Z Le; Michael N Hall; Markus A Rüegg; Claudio Punzo
Journal:  J Clin Invest       Date:  2015-03-23       Impact factor: 14.808

5.  Efficient transduction of feline neural progenitor cells for delivery of glial cell line-derived neurotrophic factor using a feline immunodeficiency virus-based lentiviral construct.

Authors:  X Joann You; Ping Gu; Jinmei Wang; Tianran Song; Jing Yang; Chee Gee Liew; Henry Klassen
Journal:  J Ophthalmol       Date:  2010-09-20       Impact factor: 1.909

6.  Oxidative stress protection by exogenous delivery of rhHsp70 chaperone to the retinal pigment epithelium (RPE), a possible therapeutic strategy against RPE degeneration.

Authors:  Astrid Subrizi; Elisa Toropainen; Eva Ramsay; Anu J Airaksinen; Kai Kaarniranta; Arto Urtti
Journal:  Pharm Res       Date:  2014-07-17       Impact factor: 4.200

Review 7.  The use of canine models of inherited retinal degeneration to test novel therapeutic approaches.

Authors:  William A Beltran
Journal:  Vet Ophthalmol       Date:  2009 May-Jun       Impact factor: 1.644

8.  Neurturin-mediated ret activation is required for retinal function.

Authors:  Milam A Brantley; Sanjay Jain; Emily E Barr; Eugene M Johnson; Jeffrey Milbrandt
Journal:  J Neurosci       Date:  2008-04-16       Impact factor: 6.167

9.  In vitro biocompatibility of degradable biopolymers in cell line cultures from various ocular tissues: extraction studies.

Authors:  Anne Huhtala; Timo Pohjonen; Lotta Salminen; Antero Salminen; Kai Kaarniranta; Hannu Uusitalo
Journal:  J Mater Sci Mater Med       Date:  2007-07-10       Impact factor: 3.896

10.  Ex vivo gene therapy using intravitreal injection of GDNF-secreting mouse embryonic stem cells in a rat model of retinal degeneration.

Authors:  Kevin Gregory-Evans; Francis Chang; Matthew D Hodges; Cheryl Y Gregory-Evans
Journal:  Mol Vis       Date:  2009-05-13       Impact factor: 2.367

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