Red light accelerates the formation of a human dermal equivalent

• Published in: Journal of biomaterials applications 2018-04, Vol.32 (9), p.1265-1275
• Main Authors: Oliveira, Anna CB, Morais, Thayz FL, Bernal, Claudia, Martins, Virginia CA, Plepis, Ana MG, Menezes, Priscila FC, Perussi, Janice R
• Format: Article
• Language: English
• Subjects: Animals; Biocompatible Materials - chemistry; Cells, Cultured; Cercopithecus aethiops; Collagen - chemistry; Dermis - cytology; Humans; Light; Porosity; Skin, Artificial; Swine; Tissue Engineering - methods; Tissue Scaffolds - chemistry; Vero Cells
• ISSN: 0885-3282; 1530-8022
• DOI: 10.1177/0885328218759385

Development of biomaterials’ substitutes and/or equivalents to mimic normal tissue is a current challenge in tissue engineering. Thus, three-dimensional cell culture using type I collagen as a polymeric matrix cell support designed to promote cell proliferation and differentiation was employed to create a dermal equivalent in vitro, as well to evaluate the photobiomodulation using red light. Polymeric matrix cell support was prepared from porcine serous collagen (1.1%) hydrolyzed for 96 h. The biomaterial exhibited porosity of 95%, a median pore of 44 µm and channels with an average distance between the walls of 78 ± 14 µm. The absorption of culture medium was 95%, and the sponge showed no cytotoxicity to Vero cells, a non-tumor cell line. Additionally, it was observed that irradiation with light at 630 nm (fluency 30 J cm−2) leads to the cellular photobiomodulation in both monolayer and human dermal equivalent (three-dimensional cell culture system). It was also verified that the cells cultured in the presence of the polymeric matrix cell support, allows differentiation and extracellular matrix secretion. Therefore, the results showed that the collagen sponge used as polymeric matrix cell support and the photobiomodulation at 630 nm are efficient for the production of a reconstructed human dermal equivalent in vitro.