Comparative proteomic analysis of human embryonic stem cell-derived and primary human retinal pigment epithelium

Human embryonic stem cell-derived retinal pigment epithelial cells (hESC-RPE) provide an unlimited cell source for retinal cell replacement therapies. Clinical trials using hESC-RPE to treat diseases such as age-related macular degeneration (AMD) are currently underway. Human ESC-RPE cells have been...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Hongisto Heidi
Jylha Antti
Nattinen Janika
Rieck Jochen
Ilmarinen Tanja
Veréb Zoltán
Aapola Ulla
Beuerman Roger
Petrovski Goran
Uusitalo Hannu
Skottman Heli
Dokumentumtípus: Cikk
Megjelent: 2017
Sorozat:SCIENTIFIC REPORTS 7 No. 1
doi:10.1038/s41598-017-06233-9

mtmt:3255498
Online Access:http://publicatio.bibl.u-szeged.hu/18316
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245 1 0 |a Comparative proteomic analysis of human embryonic stem cell-derived and primary human retinal pigment epithelium  |h [elektronikus dokumentum] /  |c  Hongisto Heidi 
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490 0 |a SCIENTIFIC REPORTS  |v 7 No. 1 
520 3 |a Human embryonic stem cell-derived retinal pigment epithelial cells (hESC-RPE) provide an unlimited cell source for retinal cell replacement therapies. Clinical trials using hESC-RPE to treat diseases such as age-related macular degeneration (AMD) are currently underway. Human ESC-RPE cells have been thoroughly characterized at the gene level but their protein expression profile has not been studied at larger scale. In this study, proteomic analysis was used to compare hESC-RPE cells differentiated from two independent hESC lines, to primary human RPE (hRPE) using Isobaric tags for relative quantitation (iTRAQ). 1041 common proteins were present in both hESC-RPE cells and native hRPE with majority of the proteins similarly regulated. The hESC-RPE proteome reflected that of normal hRPE with a large number of metabolic, mitochondrial, cytoskeletal, and transport proteins expressed. No signs of increased stress, apoptosis, immune response, proliferation, or retinal degeneration related changes were noted in hESC-RPE, while important RPE specific proteins involved in key RPE functions such as visual cycle and phagocytosis, could be detected in the hESC-RPE. Overall, the results indicated that the proteome of the hESC-RPE cells closely resembled that of their native counterparts. 
700 0 1 |a Jylha Antti  |e aut 
700 0 1 |a Nattinen Janika  |e aut 
700 0 1 |a Rieck Jochen  |e aut 
700 0 1 |a Ilmarinen Tanja  |e aut 
700 0 1 |a Veréb Zoltán  |e aut 
700 0 1 |a Aapola Ulla  |e aut 
700 0 1 |a Beuerman Roger  |e aut 
700 0 1 |a Petrovski Goran  |e aut 
700 0 1 |a Uusitalo Hannu  |e aut 
700 0 1 |a Skottman Heli  |e aut 
856 4 0 |u http://publicatio.bibl.u-szeged.hu/18316/1/41598_2017_Article_6233.pdf  |z Dokumentum-elérés