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Cellular response in rabbit eyes after human fetal RPE cell transplantation.
K Gabrielian1, A Oganesian, S C Patel
1Department of Ophthalmology and Visual Sciences Center, The University of Chicago, IL 60637, USA.
Summary
Subretinal transplantation of human fetal retinal pigment epithelial (HFRPE) cells in rabbits caused inflammatory and proliferative responses. Donor cell numbers declined after 14 days, suggesting potential rejection and highlighting the importance of cell density.
Area of Science:
- Ophthalmology
- Cell Biology
- Immunology
Background:
- Investigating cellular responses in rabbit eyes following subretinal transplantation of human fetal retinal pigment epithelial (HFRPE) cells.
- Understanding the inflammatory and proliferative reactions in xenogeneic transplantation models.
Purpose of the Study:
- To evaluate the inflammatory and proliferative cellular responses in rabbit eyes after subretinal transplantation of human fetal retinal pigment epithelial (HFRPE) cells.
- To assess the impact of HFRPE cell density on these responses and potential graft survival.
Main Methods:
- Subretinal injection of 5-Bromo-2-deoxyuridine (BrdU)-labeled HFRPE cells at varying concentrations into rabbit eyes.
- Immunohistochemistry and light microscopy were used to analyze macrophage, glial, and proliferative responses at different time points post-surgery.
Main Results:
- HFRPE cells showed irregular distribution; high-density injections led to retinal breaks, unlike low-density ones.
- Peak inflammatory response occurred between 4-14 days, with higher intensity in high-density groups.
- Host response involved macrophage and glial infiltration, followed by choroidal thickening; donor cell numbers declined after day 14.
Conclusions:
- Xenogeneic HFRPE cell transplantation elicited initial retinal cell responses, followed by choroidal involvement.
- Donor cell decline post-transplantation suggests possible immune rejection.
- The initial concentration of transplanted cells critically influences the intensity of immune and inflammatory responses.