DeepFreeze 3D‐biofabrication for Bioengineering and Storage of Stem Cells in Thick and Large‐Scale Human Tissue Analogs

Author:

Kumar Alok12ORCID,Brown Robert A.1,Roufaeil Daniel Benyamien1,Gupta Aditi13,Lipford Erika L.4,Muthusamy Divya56,Zalzman Amihai1,Hertzano Ronna43ORCID,Lowe Tao56,Stains Joseph P.7ORCID,Zalzman Michal8ORCID

Affiliation:

1. Department of Biochemistry and Molecular Biology University of Maryland School of Medicine Baltimore MD 21201 USA

2. Cardiovascular Research Center Massachusetts General Hospital (MGH) Harvard Medical School Boston MA 02114 USA

3. Neurotology Branch NIDCD, NIH Bethesda Maryland United States

4. Department of Otorhinolaryngology‐Head and Neck Surgery University of Maryland School of Medicine Baltimore MD 21201 USA

5. Department of Oral and Maxillofacial Surgery University of Maryland School of Dentistry Baltimore MD 21201 USA

6. Fischell Department of Bioengineering University of Maryland A. James Clark School of Engineering College Park MD 20742 USA

7. Department of Orthopedics University of Maryland School of Medicine Baltimore MD 21201 USA

8. Department of Biochemistry and Molecular Biology Department of Otorhinolaryngology‐Head and Neck Surgery Marlene and Stewart Greenbaum Cancer Center The Center for Stem Cell Biology and Regenerative Medicine University of Maryland School of Medicine Baltimore MD 21201 USA

Abstract

Abstract3D bioprinting holds great promise for meeting the increasing need for transplantable tissues and organs. However, slow printing, interlayer mixing, and the extended exposure of cells to non‐physiological conditions in thick structures still hinder clinical applications. Here the DeepFreeze‐3D (DF‐3D) procedure and bioink for creating multilayered human‐scale tissue mimetics is presented for the first time. The bioink is tailored to support stem cell viability, throughout the rapid freeform DF‐3D biofabrication process. While the printer nozzle is warmed to room temperature, each layer solidifies at contact with the stage (‐80 °C), or the subsequent layers, ensuring precise separation. After thawing, the encapsulated stem cells remain viable without interlayer mixing or delamination. The composed cell‐laden constructs can be cryogenically stored and thawed when needed. Moreover, it is shown that under inductive conditions the stem cells differentiate into bone‐like cells and grow for months after thawing, to form large tissue‐mimetics in the scale of centimeters. This is important, as this approach allows the generation and storage of tissue mimetics in the size and thickness of human tissues. Therefore, DF‐3D biofabrication opens new avenues for generating off‐the‐shelf human tissue analogs. It further holds the potential for regenerative treatments and for studying tissue pathologies caused by disease, tumor, or trauma.

Funder

National Institutes of Health

Publisher

Wiley

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