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Universal Peptide Hydrogel for Scalable Physiological Formation and Bioprinting of 3D Spheroids from Human Induced Pluripotent Stem Cells
Authors:Quan Li  Guangyan Qi  Xuming Liu  Jianfa Bai  Jikai Zhao  Guosheng Tang  Yu Shrike Zhang  Ruby Chen-Tsai  Meng Zhang  Donghai Wang  Yuanyuan Zhang  Anthony Atala  Jia-Qiang He  Xiuzhi Susan Sun
Affiliation:1. Department of Biological and Agricultural Engineering, Kansas State University, Manhattan, KS, 66506 USA;2. Department of Grain Science and Industries, Kansas State University, Manhattan, KS, 66506 USA;3. College of Veterinary Medicine, Kansas State University, Manhattan, KS, 66506 USA;4. Division of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Cambridge, MA, 02139 USA;5. Division of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Cambridge, MA, 02139 USA

Harvard Stem Cell Institute (HSCI), Harvard University, Cambridge, MA, 02138 USA;6. Applied StemCell, Inc., Milpitas, CA, 95035 USA;7. Department of Industrial Engineering, Kansas State University, Manhattan, KS, 66506 USA;8. Wake Forest Institute Regenerative Medicine, Wake Forest University, Winston-Salem, NC, 27151 USA;9. Department of Biomedical Sciences and Pathobiology, Virginia Tech, Blacksburg, VA, 24061 USA

Abstract:Human induced pluripotent stem cells (hiPSCs) are used for drug discoveries, disease modeling and show great potential for human organ regeneration. 3D culture methods have been demonstrated to be an advanced approach compared to the traditional monolayer (2D) method. Here, a self-healing universal peptide hydrogel is reported for manufacturing physiologically formed hiPSC spheroids. With 100 000 hiPSCs encapsulated in 500 µL hydrogel, ≈50 000 spheroids mL−1 (diameter 20–50 µm) are generated in 5 d. The spheroids in the universal peptide hydrogel are viable (85–96%) and show superior pluripotency and differentiation potential based on multiple biomarkers. Cell performance is influenced by the degradability of the hydrogel but not by gel strength. Without postprinting crosslinking aided by UV or visible lights or chemicals, various patterns are easily extruded from a simple star to a kidney-like organ shape using the universal peptide hydrogel bioink showing acceptable printability. A 20.0 × 20.0 × 0.75 mm3 sheet is finally printed with the universal peptide hydrogel bioink encapsulating hiPSCs and cultured for multiple days, and the hiPSC spheroids are physiologically formed and well maintained.
Keywords:3D culture  bioprinting  gel degradability  hiPSC physiological spheroids  self-healing hydrogels
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