|  Help  |  About  |  Contact Us

Publication : Identification of a therapeutic dose of continuously delivered erythropoietin in the eye using an inducible promoter system.

First Author  Hines-Beard J Year  2013
Journal  Curr Gene Ther Volume  13
Issue  4 Pages  275-81
PubMed ID  23773177 Mgi Jnum  J:280587
Mgi Id  MGI:6370073 Doi  10.2174/15665232113139990024
Citation  Hines-Beard J, et al. (2013) Identification of a therapeutic dose of continuously delivered erythropoietin in the eye using an inducible promoter system. Curr Gene Ther 13(4):275-81
abstractText  Erythropoietin (EPO) can protect the retina from acute damage, but long-term systemic treatment induces polycythemia. Intraocular gene delivery of EPO is not protective despite producing high levels of EPO likely due to its bellshaped dose curve. The goal of this study was to identify a therapeutic dose of continuously produced EPO in the eye. We packaged a mutated form of EPO (EPOR76E) that has equivalent neuroprotective activity as wild-type EPO and attenuated erythropoietic activity into a recombinant adeno-associated viral vector under the control of the tetracycline inducible promoter. This vector was injected into the subretinal space of homozygous postnatal 5-7 day retinal degeneration slow mice, that express the tetracycline transactivators from a retinal pigment epithelium specific promoter. At weaning, mice received a single intraperitoneal injection of doxycycline and were then maintained on water with or without doxycycline until postnatal day 60. Intraocular EPO levels and outer nuclear layer thickness were quantified and correlated. Control eyes contained 6.1 +/- 0.1 (SEM) mU/ml EPO. The eyes of mice that received an intraperitoneal injection of doxycycline contained 11.8 +/- 2.0 (SEM) mU/ml EPO-R76E. Treatment with doxycycline water induced production of 35.9 +/- 2.4 (SEM) mU/ml EPO-R76E in the eye. The outer nuclear layer was approximately 8 mum thicker in eyes of mice that received doxycycline water as compared to the control groups. Our data indicates that drug delivery systems should be optimized to deliver at least 36 mU/ml EPO into the eye since this dose was effective for the treatment of a progressive retinal degeneration.
Quick Links:
 
Quick Links:
 

Expression

Publication --> Expression annotations

 

Other

3 Bio Entities

0 Expression