Publication: Adipose derived mesenchymal stem cells partially rescue mitomycin C treated ARPE19
cells from death in co-culture condition
Authors
Singh, Amar K. ; Srivastava, Girish K. ; García-Gutiérrez, María T. ; Pastor, J. Carlos
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Publisher
F. Hernández y Juan F. Madrid. Universidad de Murcia. Departamento de Biología Celular e Histología
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DOI
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info:eu-repo/semantics/article
Description
Abstract
Age-related macular degeneration is a retinal
disease with important damage at the RPE layer. This
layer is considered a target for therapeutical approaches.
Stem cell transplantation is a promising option for retinal
diseases. Adipose derived mesenchymal stem cells
secret growth factors which might play a significant role
in RPE maintenance. This study aimed to evaluate
human AD-MSCs ability to rescue mitomycin C treated
dying ARPE19 cells in co-culture condition.
ARPE19 cells were treated with MMC (50 µg/ml,
100 µg/ml and 200 µg/ml) for 2 hours to induce cell
death. These treated cells were co-cultured with hADMSCs
in indirect co-culture system for 3 days and 3
weeks. Then the viability, growth and proliferation of
these ARPE19 cells were evaluated by a cell
viability/cytotoxicity assay kit and Alamar Blue (AB)
assay. Untreated ARPE19 cells and human skin
fibroblasts (HSF) were used as controls.
MMC blocked ARPE19 cell proliferation
significantly in 3 days and cells were almost completely
dead after 3 weeks. Cell toxicity of MMC increased
significantly with concentration. When these cells were
co-cultured with hAD-MSCs, a significant growth
difference was observed in treated cells compared to
untreated cells. hAD-MSCs rescue capacity was also
significantly higher than HSF for treated ARPE19 cells.
This study showed that hAD-MSCs rescued MMC
treated ARPE19 cells from death. It probably occurred due to undefined growth factors secreted by hAD-MSCs
in the medium, shared by treated ARPE19 cells in coculture
conditions. This study supports further
evaluation of the effect of hAD-MSCs subretinal
transplantation over the RPE degeneration process in
AMD patients.
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Citation
Histology and Histopathology, vol. 28, nº 12 (2013)
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