Microcontact printing of polydopamine on thermally expandable hydrogels for controlled cell adhesion and delivery of geometrically defined microtissues

• Published in: Acta biomaterialia 2017-10, Vol.61, p.75-87
• Main Authors: Lee, Yu Bin, Kim, Se-jeong, Kim, Eum Mi, Byun, Hayeon, Chang, Hyung-kwan, Park, Jungyul, Choi, Yu Suk, Shin, Heungsoo
• Format: Article
• Language: English
• Subjects: Animals; Assaying; Cell Adhesion; Cell Movement; Contraction; Delivery contracts; Dermis - cytology; Dimethylpolysiloxanes - chemistry; Ex vivo micro tissue formation; Extracellular matrix; Fibroblasts; Fibroblasts - cytology; Fluorescence; Glass substrates; Humans; Hydrogels; Hydrogels - chemistry; Imaging, Three-Dimensional; Indoles - chemistry; Mice; Microcontact printing; Microtechnology - methods; Microtissue delivery; Optical Imaging; Polydopamine; Polymers - chemistry; Printing; Proteins; Regenerative medicine; Skin; Substrates; Surface modification; Surface Properties; Temperature; Thermally expandable hydrogel; Tissue engineering; Tissue Engineering - methods; Viability; Water - chemistry
• ISSN: 1742-7061; 1878-7568
• DOI: 10.1016/j.actbio.2017.07.040

[Display omitted] Scaffold-free harvest of microtissue with a defined structure has received a great deal of interest in cell-based assay and regenerative medicine. In this study, we developed thermally expandable hydrogels with spatially controlled cell adhesive patterns for rapid harvest of geometrically controlled microtissue. We patterned polydopamine (PD) on to the hydrogel via microcontact printing (μCP), in linear shapes with widths of 50, 100 and 200μm. The hydrogels facilitated formation of spatially controlled strip-like microtissue of human dermal fibroblasts (HDFBs). It was possible to harvest and translocate microtissues with controlled widths of 61.4±14.7, 104.3±15.6, and 186.6±22.3μm from the hydrogel to glass substrates by conformal contact upon expansion of the hydrogel in response to a temperature change from 37 to 4°C, preserving high viability, extracellular matrix, and junction proteins. Microtissues were readily translocated in vivo to the subcutaneous tissue of mouse. The microtissues were further utilized as a simple assay model for monitoring of contraction in response to ROCK1 inhibitor. Collectively, micro-sized patterning of PD on the thermally expandable hydrogels via μCP holds promise for the development of microtissue harvesting systems that can be employed to ex vivo tissue assay and cell-based therapy. Harvest of artificial tissue with controlled cellular arrangement independently from external materials has been widely studied in cell-based assay and regenerative medicine. In this study, we developed scaffold-free harvest system of microtissues with anisotropic arrangement and controlled width by exploiting thermally expandable hydrogels with cell-adhesive patterns of polydopamine formed by simple microcontact printing. Cultured strips of human dermal fibroblasts on the hydrogels were rapidly delivered to various targets ranging from flat coverglass to mice subcutaneous tissue by thermal expansion of the hydrogel at 4°C for 10min. These were further utilized as a drug screening model responding to ROCK1 inhibitor, which imply its versatile applicability.