4.7 Article

High-Resolution Patterned Cellular Constructs by Droplet-Based 3D Printing

Journal

SCIENTIFIC REPORTS
Volume 7, Issue -, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41598-017-06358-x

Keywords

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Funding

  1. European Research Council Advanced Grant
  2. OxSyBio Ltd.
  3. Biotechnology and Biological Sciences Research Council (BBSRC) Doctoral Training Programme in Molecular Biochemistry and Chemical Biology studentship [1112403]
  4. Engineering and Physical Sciences Research Council (EPSRC) Doctoral Training Centre Grant [EP/G036780/1]
  5. EPSRC Early Career Fellowship [EP/K026720/1]
  6. Medical Research Council [MR/M010554/1]
  7. Engineering and Physical Sciences Research Council [EP/K026720/1] Funding Source: researchfish
  8. Medical Research Council [MR/M010554/1] Funding Source: researchfish
  9. EPSRC [EP/K026720/1] Funding Source: UKRI
  10. MRC [MR/M010554/1] Funding Source: UKRI

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Bioprinting is an emerging technique for the fabrication of living tissues that allows cells to be arranged in predetermined three-dimensional (3D) architectures. However, to date, there are limited examples of bioprinted constructs containing multiple cell types patterned at high-resolution. Here we present a low-cost process that employs 3D printing of aqueous droplets containing mammalian cells to produce robust, patterned constructs in oil, which were reproducibly transferred to culture medium. Human embryonic kidney (HEK) cells and ovine mesenchymal stem cells (oMSCs) were printed at tissue-relevant densities (10(7) cells mL(-1)) and a high droplet resolution of 1 nL. High-resolution 3D geometries were printed with features of <= 200 mu m; these included an arborised cell junction, a diagonal-plane junction and an osteochondral interface. The printed cells showed high viability (90% on average) and HEK cells within the printed structures were shown to proliferate under culture conditions. Significantly, a five-week tissue engineering study demonstrated that printed oMSCs could be differentiated down the chondrogenic lineage to generate cartilage-like structures containing type II collagen.

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