Novel Methods for Generating Retinal Pigment Epithelium Cells from Induced Pluripotent Stem Cells
The retinal pigment epithelial cells (RPE) make up a polarized monolayer in the vertebrate eye that separates the neural retina from the choroid, and performs a crucial role in retinal physiology by forming a blood-retinal barrier and closely interacting with photoreceptors to maintain visual function. Many ophthalmic diseases, such as age-related macular degeneration, are associated with a degeneration or deterioration of the RPE.
Researchers at NEI have developed high efficiency methods for producing retinal pigment epithelial cells (RPE) from induced pluripotent stem cells (iPSCs). The iPSCs are produced from somatic cells, including retinal pigment epithelial cells, such as fetal RPE. These methods involve producing embryoid bodies from human iPSCs, culturing the embryoid bodies using specific media to induce differentiation into RPE and growing the differentiated RPE cells in a defined media to generate human RPE cells. The investigators also developed methods for detecting RPE cells and authenticating RPE cells; determining agents that can affect the production of RPE cells from an iPSC; and identifying an agent that can increase RPE survival in response to a proteo toxic insult or stress. These novel methods and RPE cells can be useful for both pre-clinical and clinical studies involving RPE.
Competitive Advantages:
- These methods dramatically increase the efficiency of iPSC differentiation into RPE and produce superior quality RPE
- The RPE cells produced using these methods are fully authenticated
- These novel methods provide ways to perform high throughput screens with RPE cells
Commercial Applications:
- Production of RPE cells for use in screening for novel ocular therapeutics and for identifying toxic side effects of drugs
- The RPE cells produced with these methods could be used in novel cell-based therapies
- In a research setting, these cells could be used to study the pathophysiology of RPE
Patents
- US
Provisional (PRV) 61/759,988
Filed on 2013-02-01
Status: Abandoned - Patent Cooperation Treaty
(PCT) PCT/US2014/014160
Filed on 2014-01-31
Status: Expired - US
National Stage 14/764,959
Filed on 2015-07-30
Status: Abandoned - European Patent
National Stage 14705645.1
Filed on 2014-01-31
Status: Issued - Canada
National Stage 2899865
Filed on 2014-01-31
Status: Issued - Australia
National Stage 2014212230
Filed on 2014-01-31
Status: Issued - Japan
National Stage 2015-556170
Filed on 2014-01-31
Status: Issued - Denmark
European patent (EP) 14705645.1
Filed on 2014-01-31
Status: Issued - Finland
European patent (EP) 14705645.1
Filed on 2014-01-31
Status: Issued - France
European patent (EP) 14705645.1
Filed on 2014-01-31
Status: Issued - Germany
European patent (EP) 14705645.1
Filed on 2014-01-31
Status: Issued - Ireland
European patent (EP) 14705645.1
Filed on 2014-01-31
Status: Issued - The Netherlands
European patent (EP) 14705645.1
Filed on 2014-01-31
Status: Issued - United Kingdom
European patent (EP) 14705645.1
Filed on 2014-01-31
Status: Issued - European Patent
Divisional (DIV) 17197785.3
Filed on 2014-01-31
Status: Abandoned - US Patent 10,480,031
Filed on 2018-05-02
Status: Issued - Japan
Divisional (DIV) 2018-200003
Filed on 2014-01-31
Status: Abandoned - US Patent 11,441,184
Filed on 2019-09-27
Status: Issued - Australia
Divisional (DIV) 2019236596
Filed on 2019-09-23
Status: Abandoned - US
Divisional (DIV) 17/812,915
Filed on 2022-07-15
Status: Pending