April 2014
Volume 55, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2014
TRANSPLANTED mESC-DERIVED RETINAL PROGENITORS DIFFERENTIATE TO MATURE PHOTORECEPTORS IN VIVO, MIGRATE AND INTEGRATE IN THE MICE RETINA
Author Affiliations & Notes
  • Marcela Garita
    CELL THERAPY AND REGENERATIVE MEDICINE, CABIMER, Sevilla, Spain
  • Francisco Díaz-Corrales
    CELL THERAPY AND REGENERATIVE MEDICINE, CABIMER, Sevilla, Spain
  • Slaven Erceg
    CELL THERAPY AND REGENERATIVE MEDICINE, CABIMER, Sevilla, Spain
  • Shomi Bhattacharya
    CELL THERAPY AND REGENERATIVE MEDICINE, CABIMER, Sevilla, Spain
  • Footnotes
    Commercial Relationships Marcela Garita, None; Francisco Díaz-Corrales, None; Slaven Erceg, None; Shomi Bhattacharya, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science April 2014, Vol.55, 3988. doi:
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      Marcela Garita, Francisco Díaz-Corrales, Slaven Erceg, Shomi Bhattacharya; TRANSPLANTED mESC-DERIVED RETINAL PROGENITORS DIFFERENTIATE TO MATURE PHOTORECEPTORS IN VIVO, MIGRATE AND INTEGRATE IN THE MICE RETINA. Invest. Ophthalmol. Vis. Sci. 2014;55(13):3988.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: Retinal dystrophies characterized by the progressive degeneration of photoreceptors are the leading causes of incurable blindness. Due to the limited capacity of the mammalian retina to regenerate using embryonic stem cells (ESC) as an unlimited source to replenish the lost cells has represented a main objective for the scientific community. Despite great advances in the field of differentiation of ESC towards photoreceptors in the recent years, few drawbacks remain unresolved. Such as, efficiency, purity of the population and the constant worry that once differentiated, cells could not be able to integrate into the host retina

Methods: We optimized a new protocol to differentiate mouse ESC (mESC), involving the control of the oxygen tension to mimic the retinal niche conditions, as well as the manipulation of key signaling pathways involved during normal retinal development. The retinal progenitor cells generated were subretinally transplanted in order to evaluate their migration and integration capacities by immunohistochemistry analysis

Results: Hypoxia increases the efficiency of differentiation towards photoreceptors, but as well it improves the modeling of retinogenesis in vitro, by decreasing the time necessary to acquire each specific phenotype. Transcription factors associated to each stage of retinal differentiation such as eye field (Rax, Six3), optic cup (Pax6, Mitf, Chx10), photoreceptor precursors (Nrl, Crx) and even mature photoreceptors (Rhodopsin, Recoverin and Opsin-S) were upregulated earlier and their levels of expression were significantly higher than those reached under normoxic conditions as determined by qPCR. Moreover, when photoreceptor precursors derived from mESC cells following our protocol under hypoxia were transplanted into the subretinal space of wild type mice they differentiated mainly towards Recoverin/Rhodopsin positive cells, migrate and integrate into the host retina and in some cases acquired the morphology of mature rods with formation of structures suggesting outer segments

Conclusions: Our results demonstrate that hypoxia increases the yield of retinal phenotypes from mESC, including mature phenotypes. Moreover, in vivo experiments demonstrated that hypoxia promotes the survival of the grafted cells, allowing the retinal progenitors to differentiate towards photoreceptors, migrate and integrate in the mice retina

Keywords: 721 stem cells • 694 retinal culture • 741 transplantation  
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