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Development of lacrimal gland spheroids for lacrimal gland tissue regeneration
Author(s) -
Massie Isobel,
Spaniol Kristina,
Barbian Andreas,
Geerling Gerd,
Metzger Marco,
Schrader Stefan
Publication year - 2018
Publication title -
journal of tissue engineering and regenerative medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.835
H-Index - 72
eISSN - 1932-7005
pISSN - 1932-6254
DOI - 10.1002/term.2631
Subject(s) - spheroid , matrigel , mesenchymal stem cell , microbiology and biotechnology , pathology , chemistry , biology , cell culture , angiogenesis , cancer research , medicine , genetics
Severe dry eye syndrome resulting from lacrimal gland (LG) dysfunction can cause blindness, yet treatments remain palliative. In vitro reconstruction of LG tissue could provide a curative treatment. We aimed to combine epithelial cells with endothelial cells and mesenchymal stem cells (MSCs) to form a 3D functional unit. Epithelial cells and MSCs were isolated from porcine LG; endothelial cells were isolated from human foreskin. MSCs were characterised (flow cytometry and differentiation potential assays). All 3 cell types were combined on Matrigel and spheroid formation observed. Spheroids were characterised [immunohistochemistry (IHC) and transmission electron microscopy] and function assessed (β‐hexosaminidase assay). Spheroids were transferred to decellularised jejunum (SIS‐Muc) in dynamic cultures for 1 week before further characterisation. MSCs did not express CD31 but expressed CD44 and CD105 and differentiated towards osteogenic and adipogenic lineages. Spheroids formed on Matrigel within 18 hr, contracting to ~10% of the well area ( p < .005). IHC revealed presence of all 3 cells within spheroids. Transmission electron microscopy revealed cell–cell contacts and polarisation at the apical surface. In static cultures, function was increased in spheroids cf. monolayer controls ( p < .05) but over 72 hr, spheroid function ( p < .05), viability ( p < .05), and proliferation decreased, whilst apoptosis increased. On SIS‐Muc under dynamic culture, however, spheroids continued to proliferate to repopulate SIS‐Muc. IHC revealed LG epithelial cells coexpressing pan‐cytokeratin and lysozyme, as well as endothelial cells and MSCs and cells remained capable of responding to carbachol ( p < .05). These spheroids could form the basis of a regenerative medicine treatment approach for dry eye syndrome. In vivo studies are required to evaluate this further.