Volume 15, Issue 1 pp. 37-48
RESEARCH ARTICLE

Validation of an implantable bioink using mechanical extraction of human skin cells: First steps to a 3D bioprinting treatment of deep second degree burn

Adeline Desanlis

Adeline Desanlis

Hospices Civils de Lyon, Banque de Tissus et Cellules, Groupement Hospitalier Edouard Herriot, Lyon, France

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Marion Albouy

Marion Albouy

LabSkin Creations, Edouard Herriot Hospital, Lyon, France

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Patricia Rousselle

Patricia Rousselle

Laboratoire de Biologie Tissulaire et Ingénierie Thérapeutique, UMR 5305, CNRS - Université Lyon 1, Institut de Biologie et Chimie des Protéines, SFR BioSciences Gerland-Lyon Sud, Lyon, France

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Amélie Thépot

Amélie Thépot

LabSkin Creations, Edouard Herriot Hospital, Lyon, France

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Morgan Dos Santos

Morgan Dos Santos

LabSkin Creations, Edouard Herriot Hospital, Lyon, France

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Céline Auxenfans

Céline Auxenfans

Hospices Civils de Lyon, Banque de Tissus et Cellules, Groupement Hospitalier Edouard Herriot, Lyon, France

Laboratoire de Biologie Tissulaire et Ingénierie Thérapeutique, UMR 5305, CNRS - Université Lyon 1, Institut de Biologie et Chimie des Protéines, SFR BioSciences Gerland-Lyon Sud, Lyon, France

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Christophe Marquette

Corresponding Author

Christophe Marquette

3d.FAB, Univ Lyon, Université Lyon 1, CNRS, INSA, CPE-Lyon, ICBMS, UMR 5246, Villeurbanne, France

Correspondence

Christophe Marquette, 3d.FAB, Univ Lyon, Université Lyon 1, CNRS, INSA, CPE-Lyon, ICBMS, UMR 5246, 43, Bd du 11 novembre 1918, 69622 Villeurbanne cedex, France

Email: [email protected]

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First published: 10 November 2020
Citations: 27

Abstract

Clinical grade cultured epithelial autograft (CEA) are routinely used to treat burns covering more than 60% of the total body surface area. However, although the epidermis may be efficiently repaired by CEA, the dermal layer, which is not spared in deep burns, requires additional treatment strategies. Our aim is to develop an innovative method of skin regeneration based on in situ 3D bioprinting of freshly isolated autologous skin cells. We describe herein bioink formulation and cell preparation steps together with experimental data validating a straightforward enzyme-free protocol of skin cell extraction. This procedure complies with both the specific needs of 3D bioprinting process and the stringent rules of good manufacturing practices. This mechanical extraction protocol, starting from human skin biopsies, allows harvesting a sufficient amount of both viable and growing keratinocytes and fibroblasts. We demonstrated that a dermis may be reconstituted in vitro starting from a medical grade bioink and mechanically extracted skin cells. In these experiments, proliferation of the extracted cells can be observed over the first 21 days period after 3D bioprinting and the analysis of type I collagen exhibited a de novo production of extracellular matrix proteins. Finally, in vivo experiments in a murine model of severe burn provided evidences that a topical application of our medical grade bioink was feasible and well-tolerated. Overall, these results represent a valuable groundwork for the design of future 3D bioprinting tissue engineering strategies aimed at treating, in a single intraoperative step, patients suffering from extended severe burns.

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