AI Article Synopsis

  • - The study aimed to examine how fenretinide affects aquaporin (AQP) expression in ARPE-19 cells as they change into neuronal-like cells over a week-long treatment.
  • - Results showed that while control ARPE-19 cells had AQP1, AQP4, AQP6, and AQP11 at the mRNA level, only AQP4, AQP6, and AQP11 were present at the protein level; fenretinide treatment led to significant morphological changes and reduced retinal markers while increasing neuronal markers.
  • - Specifically, the study found that during this transdifferentiation process, the levels of AQP4 and AQP6 were significantly decreased in both m

Article Abstract

Purpose: The goal of this study was to investigate the modifications of aquaporin (AQP) expression in ARPE-19 cells in response to fenretinide-induced transdifferentiation into neuronal-like cells

Methods: ARPE-19 cells were treated daily for 7 days with 3 μm fenretinide or dimethyl sulphoxide as control. mRNA and protein expression were evaluated by real-time quantitative PCR, Western blot analysis and immunofluorescence.

Results: Control ARPE-19 cells expressed AQP1, AQP4, AQP6 and AQP11 at the mRNA level, but only AQP4, AQP6 and AQP11 at the protein level. Fenretinide induced the transdifferentiation of ARPE-19 cells into neuronal-like cells. Indeed, fenretinide induced morphological changes similar to neurons characterized by elongated cell body and the formation of neurite branching. Moreover, ARPE-19 cells transdifferentiated to neuron-like cells were characterized by significant decrease in retinal pigmented epithelium markers, for example cytokeratin 8 and cellular retinaldehyde-binding protein, as well as an increase in neuronal markers such as synaptophysin and calretinin. AQP4 expression, at both mRNA and protein levels, and AQP6 expression, only at protein level, were significantly decreased in ARPE-19 cells transdifferentiated into neuronal-like cells.

Conclusions: The expression of AQP4 and AQP6 is downregulated during fenretinide-induced transdifferentiation.

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Source
http://dx.doi.org/10.1111/aos.12837DOI Listing

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