(871.3) Epithelial monolayer development and tight junction assembly on nanopillar arrays

Poster Board Number: E224

Jose Yeste (Brigham and Womens Hospital, Harvard Medical School, Brigham and Womens Hospital, Harvard Medical School), Xavi Illa (Instituto de Microelectrónica de Barcelona, IMB-CNM (CSIC), Instituto de Microelectrónica de Barcelona, IMB-CNM (CSIC)), Nitesh Shashikanth (Brigham and Womens Hospital, Harvard Medical School), Anton Guimerà-Brunet (Instituto de Microelectrónica de Barcelona, IMB-CNM (CSIC), Instituto de Microelectrónica de Barcelona, IMB-CNM (CSIC), Instituto de Microelectrónica de Barcelona, IMB-CNM (CSIC)), Rosa Villa (Instituto de Microelectrónica de Barcelona, IMB-CNM (CSIC), Instituto de Microelectrónica de Barcelona, IMB-CNM (CSIC)), Jerrold Turner (Brigham and Womens Hospital, Harvard Medical School)

Nanostructured materials provide an outstanding opportunity to both stimulate and measure cellular processes. In the context of tight junctions, it was previously reported that transient application of a nanotopographic surface over the apical brush border membrane of epithelial monolayers triggers redistribution of ZO-1, claudins, and F-actin that increases paracellular macromolecular flux. In excitable tissues, nanomaterials have been used to apply and measure electrical signals, such action potentials. As a first step towards translating these technologies for use in analysis of epithelial function, we sought to culture monolayers composed of transporting epithelia over nanopillar arrays without perturbing cellular structure or function. Madin-Darby Canine kidney I (MDCKI) cells were cultured on collagen-coated silicon chips with ~1.5 µm diameter nanopillar arrays. Fluorescence and scanning electron microscopy were used to assess the impact of height on nanopillar-epithelial interactions. Monolayers formed over and were largely unaffected by short nanopillars. These nanopillars were located beneath basal epithelial surfaces and were not preferentially located within lateral intercellular spaces or beneath ZO-1-containing junctions. In contrast, tall nanopillars that exceeded cell height disrupted MDCK monolayer growth. Cells interacted with, encircled, and extended cytoplasm over the top of tall nanopillars, and dense ZO-1 and F-actin accumulations occasionally surrounded apical membranes adjacent to nanopillars.  Finally, when grown over arrays composed of nanopillars 1 – 2 µm less than cell height, MDCKI grew more often between nanopillars. As a result, nanopillars were more frequently present within lateral intercellular spaces beneath junctions. Apical complex structure was intact, as assessed by fluorescence microscopy of ZO-1, occludin, claudin-2, F-actin, and E-cadherin. Apical microvilli were also unaffected. These data establish the conditions required for growth of mature, correctly assembled epithelial monolayers in which nanopillars are present within lateral intercellular spaces. This sets the stage for synthesis of functionalized nanopillar arrays for perturbation and analysis of epithelial biology.

Supported by R01 DK068271, R01 DK061931, the European Unionamp;rsquo;s Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie grant agreement No 896293, and the Spanish ICTS Network MICRONANOFABS partially supported by MICINN and the ICTS amp;lsquo;NANBIOSISamp;rsquo;, more specifically by the Micro-NanoTechnology Unit of the CIBER in Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN) at the IMB-CNM.