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Human fetal keratocytes have multipotent characteristics in the developing avian embryo
Jennifer R Chao1, Marianne E Bronner, Peter Y Lwigale
1Department of Ophthalmology, University of Washington, Seattle, Washington, USA.
Stem Cells and Development
|March 7, 2013
Summary
Human fetal keratocytes (HFKs) can differentiate into neural crest derivatives, including corneal endothelium and stromal keratocytes, when transplanted into embryonic chick environments. This suggests potential for regenerative medicine applications using these multipotent cells.
Area of Science:
- Developmental Biology
- Stem Cell Biology
- Ophthalmology
Background:
- Human corneal stem cells show multipotency in vitro.
- Human corneal keratocytes' multipotency in vivo remains unproven.
- Neural crest cells are crucial for developing various tissues.
Purpose of the Study:
- To investigate the multipotency of human fetal keratocytes (HFKs).
- To assess HFKs' differentiation into neural crest-derived tissues in an embryonic setting.
- To explore potential regenerative medicine applications.
Main Methods:
- HFKs were injected into chick embryos at specific developmental stages (embryonic days 1.5 and 3).
- Injections targeted cranial mesenchyme near the neural tube and periocular mesenchyme.
- Human cells were identified using the HuNu marker; differentiation was assessed via immunofluorescence.
Main Results:
- HuNu-positive HFKs integrated near migratory neural crest cells and in cardiac mesenchyme.
- HFKs differentiated into smooth muscle cells, stromal keratocytes, and corneal endothelium.
- HFKs did not form neurons, even when located within the trigeminal ganglion.
Conclusions:
- Human fetal keratocytes exhibit multipotency and can differentiate into specific neural crest derivatives.
- HFKs respond to embryonic cues, generating corneal endothelium and stromal keratocytes.
- These findings support the feasibility of using HFKs for regenerative medicine strategies.
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