A secretory cell type develops alongside multiciliated cells, ionocytes and goblet cells, and provides a protective, anti-infective function in the frog embryonic mucociliary epidermis

• DOI: 10.1242/dev.102426
• Publication Date: 2014-03-06T05:01:51Z
• Authors: Eamon Dubaissi; Karine Rousseau; Robert Lea; Ximena Soto; Siddarth Nardeosingh; Axel Schweickert; Enrique Amaya; David J. Thornton; Nancy Papalopulu
• Keywords: Hepatocyte Nuclear Factor 3-alpha; 0301 basic medicine; Embryo, Nonmammalian; Xenopus; Mucociliary; 03 medical and health sciences; Animals; Cilia; Research Articles; Glycoproteins; Xenopus epidermis; Ions; Secretory Pathway; Secretory Vesicles; Mucins; Cell Differentiation; FoxA1; Immunity, Innate; 3. Good health; Mucus; Larva; Otogelin; Goblet Cells; Epidermis; Infection; ResearchInstitutes_Networks_Beacons/lydia_becker_institute_of_immunology_and_inflammation; name=Lydia Becker Institute

The larval epidermis of Xenopus is a bilayered epithelium, which is an excellent model system for the study of the development and function of mucosal and mucociliary epithelia. Goblet cells develop in the outer layer while multiciliated cells and ionocytes sequentially intercalate from the inner to the outer layer. Here, we identify and characterise a fourth cell type, the small secretory cell (SSC). We show that the development of these cells is controlled by the transcription factor Foxa1 and that they intercalate into the outer layer of the epidermis relatively late, at the same time as embryonic hatching. Ultrastructural and molecular characterisation shows that these cells have an abundance of large apical secretory vesicles, which contain highly glycosylated material, positive for binding of the lectin, peanut agglutinin, and an antibody to the carbohydrate epitope, HNK-1. By specifically depleting SSCs, we show that these cells are crucial for protecting the embryo against bacterial infection. Mass spectrometry studies show that SSCs secrete a glycoprotein similar to Otogelin, which may form the structural component of a mucus-like protective layer, over the surface of the embryo, and several potential antimicrobial substances. Our study completes the characterisation of all the epidermal cell types in the early tadpole epidermis and reinforces the suitability of this system for the in vivo study of complex epithelia, including investigation of innate immune defences.