Publication: Ex vivo 3D human corneal stroma model for Schnyder corneal dystrophy - role of autophagy in its pathogenesis and resolution
Authors
Szabó, Dóra Júlia ; Nagymihály, Richárd ; Veréb, Zoltán ; Josifovska, Natasha ; Noer, Agate ; Liskova, Petra ; Facskó, Andrea ; Moe, Morten C. ; Petrovski, Goran
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Publisher
Universidad de Murcia. Departamento de Biología Celular e Histología
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DOI
DOI: 10.14670/HH-11-928
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info:eu-repo/semantics/article
Description
Abstract
Introduction. Multilamellar bodies (MLBs)
are concentric cytoplasmic membranes which form
through an autophagy-dependent mechanism. In the
cornea, the presence of MLBs is associated with
Schnyder corneal dystrophy (SCD). Ex vivo 3D
modelling of the corneal stroma and SCD can help study
pathogenesis and resolution of the disorder. Methods.
Corneal stroma explants were isolated from cadavers
and cultivated long-term for more than 3 months to
achieve spontaneous 3D outgrowth of corneal stromaderived mesenchymal stem-like cells (CSMSCs). The
3D tissues were then examined by transmission electron
microscopy (TEM) for presence of MLBs, and by
immunofluorescent labelling against markers for
autophagy (p62, LC3). Autophagy was induced by
classical serum starvation or rapamycin (RAP) treatment
(50nM), and inhibited by the autophagy inhibitor 3-
methyladenine (3-MA, 10 mM) for 24 hours. Results.
CSMSCs can form spontaneously 3D outgrowths over a
3-4 weeks period, depositing their own extracellular
matrix containing collagen I. TEM confirmed the
presence of MLBs in the long-term (>3 months) 3D
cultures, which became more abundant under starvation
and RAP treatment, and decreased in number under
autophagy inhibition with 3-MA. The presence of
autophagy and its disappearance could be confirmed by
an inversely related increase and decrease in the
expression of LC3 and p62, respectively. Conclusions.
MLB formation in long-standing CSMSC cultures could
serve as a potential ex vivo model for studying corneal
stroma diseases, including SCD. Inhibition of autophagy
can decrease the formation of MLBs, which may lead to
a novel treatment of the disease in the future.
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Citation
Histology and Histopathology, Vol.33, nº5, (2018)
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