Abstract

Due to the limited number of organ donors, 3D printing of organs is a promising technique. Tissue engineering is increasingly using xenogeneic material for this purpose. This study was aimed at assessing the safety of decellularized porcine pancreas, together with the analysis of the risk of an undesirable immune response. We tested eight variants of the decellularization process. We determined the following impacts: rinsing agents (PBS/NH3·H2O), temperature conditions (4 °C/24 °C), and the grinding method of native material (ground/cut). To assess the quality of the extracellular matrix after the completed decellularization process, analyses of the following were performed: DNA concentration, fat content, microscopic evaluation, proteolysis, material cytotoxicity, and most importantly, the Triton X-100 content. Our analyses showed that we obtained a product with an extremely low detergent content with negligible residual DNA content. The obtained results confirmed the performed histological and immuno-fluorescence staining. Moreover, the TEM microscopic analysis proved that the correct collagen structure was preserved after the decellularization process. Based on the obtained results, we chose the most favorable variant in terms of quality and biology. The method we chose is an effective and safe method that gives a chance for the development of transplant and regenerative medicine.

Highlights

  • These research approaches are not widely described in the literature, wherefore we developed a new way for determining the content of triton X-100 in decellularized extracellular matrices (dECMs) and conducted cytotoxicity tests to confirm the biological quality of decellularized tissue

  • The method of preparing the material for the decellularization process significantly affected the final concentration of genetic material in the obtained dECM

  • Sci. 2021, 22, 7005 method of preparing the material for the decellularization process significantly affected the final concentration of genetic material in the obtained dECM

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Summary

Introduction

The shortage of organs for transplantation condemns many patients to arduous substitution treatment, severe complications, and even death [1]. One of the branches of tissue engineering that is currently thriving is 3D bioprinting. This pioneering technology allows the production of biomimetic constructs with a heterogeneity of tissue composition [6,7]. The extracellular matrix (ECM) is a naturally occurring scaffold secreted by the resident cells of each tissue and organ, which forms a cellular microenvironment composed of glycoproteins, collagens, glycosaminoglycans, and proteoglycans [10]. ECM proteins (collagens, proteoglycans, and glycoproteins) and their spatial structures can determine cell behavior and viability through communication with the intracellular cytoskeleton [13,14]

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