In vitro comparison of human plasma-based and self-assembled tissue-engineered skin substitutes: two different manufacturing processes for the treatment of deep and difficult to heal injuries

Author:

Sierra-Sánchez Álvaro1234ORCID,Magne Brice123ORCID,Savard Etienne123ORCID,Martel Christian123ORCID,Ferland Karel123ORCID,Barbier Martin A123ORCID,Demers Anabelle123ORCID,Larouche Danielle123ORCID,Arias-Santiago Salvador456ORCID,Germain Lucie123ORCID

Affiliation:

1. LOEX Tissue Engineering Laboratory and Department of Surgery , Faculty of Medicine, , 1401 18e rue, Québec (Québec) G1J 1Z4 , Canada

2. Université Laval , Faculty of Medicine, , 1401 18e rue, Québec (Québec) G1J 1Z4 , Canada

3. CHU de Québec – Université Laval Research Center, Division of Regenerative Medicine , 1401 18e rue, Québec (Québec) G1J 1Z4 , Canada

4. Unidad de Producción Celular e Ingeniería Tisular (UPCIT), Virgen de las Nieves University Hospital, ibs . GRANADA, Andalusian Network for the design and translation of Advanced Therapies, Av. de las Fuerzas Armadas, Nº2, 4ª Planta Ed. de Gobierno, 18014, Granada, Spain

5. Department of Dermatology, Virgen de las Nieves University Hospital , Av. Madrid, Nº11–15, 18012, Granada , Spain

6. Department of Dermatology, Faculty of Medicine, University of Granada , Av. de la Investigación, Nº11, 18016, Granada , Spain

Abstract

Abstract Background The aim of this in vitro study was to compare side-by-side two models of human bilayered tissue-engineered skin substitutes (hbTESSs) designed for the treatment of severely burned patients. These are the scaffold-free self-assembled skin substitute (SASS) and the human plasma-based skin substitute (HPSS). Methods Fibroblasts and keratinocytes from three humans were extracted from skin biopsies (N = 3) and cells from the same donor were used to produce both hbTESS models. For SASS manufacture, keratinocytes were seeded over three self-assembled dermal sheets comprising fibroblasts and the extracellular matrix they produced (n = 12), while for HPSS production, keratinocytes were cultured over hydrogels composed of fibroblasts embedded in either plasma as unique biomaterial (Fibrin), plasma combined with hyaluronic acid (Fibrin-HA) or plasma combined with collagen (Fibrin-Col) (n/biomaterial = 9). The production time was 46–55 days for SASSs and 32–39 days for HPSSs. Substitutes were characterized by histology, mechanical testing, PrestoBlue™-assay, immunofluorescence (Ki67, Keratin (K) 10, K15, K19, Loricrin, type IV collagen) and Western blot (type I and IV collagens). Results The SASSs were more resistant to tensile forces (p-value < 0.01) but less elastic (p-value < 0.001) compared to HPSSs. A higher number of proliferative Ki67+ cells were found in SASSs although their metabolic activity was lower. After epidermal differentiation, no significant difference was observed in the expression of K10, K15, K19 and Loricrin. Overall, the production of type I and type IV collagens and the adhesive strength of the dermal-epidermal junction was higher in SASSs. Conclusions This study demonstrates, for the first time, that both hbTESS models present similar in vitro biological characteristics. However, mechanical properties differ and future in vivo experiments will aim to compare their wound healing potential.

Funder

Instituto de Salud Carlos III

Regional Government of Andalusia

Canadian Institutes for Health Research

Publisher

Oxford University Press (OUP)

Subject

Critical Care and Intensive Care Medicine,Dermatology,Biomedical Engineering,Emergency Medicine,Immunology and Allergy,Surgery

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