Rescuing ocular development in an anophthalmic pig by blastocyst complementation.
Hongyong ZhangJiaojiao HuangZechen LiGuosong QinNan ZhangTang HaiQianlong HongQiantao ZhengYing ZhangRuigao SongJing YaoChunwei CaoJianguo ZhaoQi ZhouPublished in: EMBO molecular medicine (2019)
Porcine-derived xenogeneic sources for transplantation are a promising alternative strategy for providing organs for treatment of end-stage organ failure in human patients because of the shortage of human donor organs. The recently developed blastocyst or pluripotent stem cell (PSC) complementation strategy opens a new route for regenerating allogenic organs in miniature pigs. Since the eye is a complicated organ with highly specialized constituent tissues derived from different primordial cell lineages, the development of an intact eye from allogenic cells is a challenging task. Here, combining somatic cell nuclear transfer technology (SCNT) and an anophthalmic pig model (MITF L 247S/L247S), allogenic retinal pigmented epithelium cells (RPEs) were retrieved from an E60 chimeric fetus using blastocyst complementation. Furthermore, all structures were successfully regenerated in the intact eye from the injected donor blastomeres. These results clearly demonstrate that not only differentiated functional somatic cells but also a disabled organ with highly specialized constituent tissues can be generated from exogenous blastomeres when delivered to pig embryos with an empty organ niche. This system may also provide novel insights into ocular organogenesis.
Keyphrases
- induced apoptosis
- cell cycle arrest
- cell therapy
- stem cells
- endothelial cells
- gene expression
- end stage renal disease
- single cell
- palliative care
- endoplasmic reticulum stress
- chronic kidney disease
- cell death
- ejection fraction
- newly diagnosed
- peritoneal dialysis
- mass spectrometry
- induced pluripotent stem cells
- drinking water
- pluripotent stem cells
- bone marrow
- germ cell