Abstract

Regenerative medicine research requires animal experiments to evaluate treatment effects. According to the 3Rs prin­ciples, alternative models have been developed and utilized to evaluate the efficacy and safety of new products. Three-dimensional (3D) cell cultures have been recognized for their relevant structures and biological functions that are akin to native tissues. They can better represent in vivo conditions than two-dimensional (2D) cell cultures. Herein, we present a fast and simple technique for the construction of 3D dermal fibroblasts (3D-DFs) without exogenous scaffolds. The 3D-DFs can be obtained within 3 days by seeding DFs at a level that exceeds their confluent density and culturing them in the presence of ascorbic acid. The 3D-DFs have a compact, multilayer structure as revealed by histology and their collagen content is drastically increased compared to the monolayer. The 3D-DF-derived extracellular matrix can serve for 3D culturing of other cells. A gap closure assay was performed with the 3D-DFs to represent a 3D-wounded dermal model. Interestingly, the multilayered structure of the 3D-DFs could be regenerated after wounding even when cultured in the absence of ascorbic acid. Moreover, skin grafting using the 3D-DFs was demonstrated in vitro using wounded in vitro human full-thickness skin models. The 3D-DFs will be potentially useful for regenerative medicine and as tissue models for in vitro studies.

Highlights

  • In vivo tissues are composed of a complex system of three-dimensional (3D) cellular multilayers of various types of cells and extracellular matrix (ECM)

  • Cross-sectional images of hematoxylin & eosin (H&E) stained dermal fibroblasts (DFs) cultured without SAP revealed a loose structure, where most of the cells did not adhere to each other (Fig. S1A2)

  • We present a simple concept for the fast construction of scaffold-free 3D tissues by cellular self-assembly

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Summary

Introduction

In vivo tissues are composed of a complex system of three-dimensional (3D) cellular multilayers of various types of cells and extracellular matrix (ECM). Alternatives to animal experiments have been developed that include in vitro and ex vivo approaches. Since two-dimensional (2D) in vitro models composed of a monolayer of cells poorly reflect the in vivo situation, recent research has realized the significance of 3D cultures over 2D cultures due to their more relevant structure and cellular functions compared to native tissues (Griffith and Swartz, 2006; Bokhari et al, 2007; Onoe et al, 2013; Knight and Przyborski, 2015). Scaffolds derived from various biomaterials can be applied for the construction of 3D tissues (Bokhari et al, 2007; Lee et al, 2009; Kim et al, 2015). The presence of these scaffold materials can disturb the tissue remodeling and functions (Anderson et al, 2008; Alaribe et al, 2016), and can induce undesired foreign body reactions following implantation

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