Induction of in vivo-like ciliation in confluent monolayers of re-differentiated equine oviduct epithelial cells

Author:

Leemans Bart1234,Gadella Bart M345262,Marchand Josephine H E A M12,Van Soom Ann34,Stout Tom A E12

Affiliation:

1. Department of Clinical Sciences , Faculty of Veterinary Medicine, , Utrecht, The Netherlands

2. Utrecht University , Faculty of Veterinary Medicine, , Utrecht, The Netherlands

3. Department of Internal Medicine , Reproduction, Population Health, Faculty of Veterinary Medicine, , Ghent, Belgium

4. Ghent University , Reproduction, Population Health, Faculty of Veterinary Medicine, , Ghent, Belgium

5. Biomolecular Health Sciences , Faculty of Veterinary Medicine, , Utrecht, The Netherlands

6. Population Health Sciences , Faculty of Veterinary Medicine, , Utrecht, The Netherlands

Abstract

Abstract We recently developed re-differentiated equine oviduct epithelial cell (REOEC) monolayers demonstrating various in vivo morphological characteristics, but lacking secondary ciliation. In this study, we evaluated the effects of fetal bovine serum, reproductive steroid hormones, Wnt- and Notch ligands and inhibitors, and different EOEC seeding densities, in both conventional wells and on microporous membranes, on EOEC morphology and, in particular, secondary ciliation. REOEC monolayers were assessed by confocal microscopy after combined staining of nuclei, cilia, and the cytoskeleton. Only Wnt ligands, Notch inhibitors and oviduct explant cell concentration affected EOEC morphology. Undesirable epithelial-mesenchymal transition was observed in REOEC monolayers exposed to Wnt3a containing medium and Wnt ligand CHIR 99021. With respect to secondary ciliation, only the combined effect of oviduct explant cell concentration and Notch inhibition steered REOEC monolayers to in vivo-like ciliation patterns. De-differentiated EOECs, formed 10 days after oviduct explant cell seeding, were reseeded on inserts; only at initial oviduct explant cell concentrations of 1 and 5 × 106 cells per well was the formation of REOEC monolayers with a high rate of diffuse ciliation supported. Within 1 month after air-liquid interface introduction, >40% and >20% of the REOECs showed secondary cilia, respectively. At higher oviduct explant cell seeding densities secondary ciliation was not supported after re-differentiation. Additionally, Notch inhibition helped boost secondary ciliation rates to >60% in REOEC monolayers with diffuse ciliation only. These monolayers demonstrated higher clathrin expression under follicular phase conditions. Overall, the ciliated REOEC monolayers better resemble in vivo oviduct epithelial cells than previous models.

Funder

Research Foundation Flanders

EU COST Action

Publisher

Oxford University Press (OUP)

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