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Effects of corneal stromal cell- and bone marrow-derived endothelial progenitor cell-conditioned media on the proliferation of corneal endothelial cells. | LitMetric

AI Article Synopsis

  • The study aimed to investigate how different types of conditioned media affect the growth of corneal endothelial cells (CECs) and identify which media is most effective.
  • Rat CECs and other cell types were cultured in vitro, and the effects of conditioned media from corneal stromal cells, bone marrow-derived endothelial progenitor cells, and bone marrow-derived mesenchymal stem cells were analyzed for their influence on cell morphology and gene/protein expression.
  • Results showed that CECs retained their healthy shape and exhibited increased expression of vital proteins in the presence of conditioned media, with the strongest proliferation effect observed from the conditioned media of corneal stromal cells.

Article Abstract

Aim: To explore the effects of conditioned media on the proliferation of corneal endothelial cells (CECs) and to compare the efficiency of different conditioned media (CM).

Methods: Rat CECs, corneal stromal cells (CSCs), bone marrow-derived endothelial progenitor cells (BEPCs), and bone marrow-derived mesenchymal stem cells (BMSCs) were isolated and cultured in vitro. CM was collected from CSCs, BEPCs, and BMSCs. CECs were cultivated in different culture media. Cell morphology was recorded, and gene and protein expression were analyzed.

Results: After grown in CM for 5d, CECs in each experimental group remained polygonal, in a cobblestone-like monolayer arrangement. Immunocytofluorescence revealed positive expression of Na(+)/K(+)-ATP, aquaporin 1 (AQP1), and zonula occludens 1 (ZO-1). Based on quantitative polymerase chain reaction (qPCR) analysis, Na(+)/K(+)-ATP expression in CSC-CM was notably upregulated by 1.3-fold (±0.036) (P<0.05, n=3). The expression levels of ZO-1, neuron specific enolase (NSE), Vimentin, paired homebox 6 (PAX6), and procollagen type VIII (COL8A1) were notably upregulated in each experimental group. Each CM had a positive effect on CEC proliferation, and CSC-CM had the strongest effect on proliferation.

Conclusion: CSC-CM, BEPC-CM, and BMSC-CM not only stimulated the proliferation of CECs, but also maintained the characteristic differentiated phenotypes necessary for endothelial functions. CSC-CM had the most notable effect on CEC proliferation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4844038PMC
http://dx.doi.org/10.18240/ijo.2016.03.02DOI Listing

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