Schwarz Silke, Kuth Sonja, Distler Thomas, Gögele Clemens, Stölzel Katharina, Detsch Rainer, Boccaccini Aldo R, Schulze-Tanzil Gundula
Department of Anatomy and Cell Biology, Paracelsus Medical University, Nuremberg and Salzburg, Prof.-Ernst-Nathan Str. 1, 90419 Nuremberg, Germany.
Department of Anatomy and Cell Biology, Paracelsus Medical University, Nuremberg and Salzburg, Prof.-Ernst-Nathan Str. 1, 90419 Nuremberg, Germany; Institute of Biomaterials, University of Erlangen-Nuremberg, Cauerstr. 6, 91058 Erlangen, Germany.
Mater Sci Eng C Mater Biol Appl. 2020 Nov;116:111189. doi: 10.1016/j.msec.2020.111189. Epub 2020 Jun 12.
As cartilage is one of the few tissues in the human body that is not vascularized, the body has very limited capabilities to repair cartilage defects. Hence, novel condro-instructive biomaterials facilitating cartilage formation by implanted chondrocytes are required. In this work, an oxidized alginate-gelatin hydrogel system, alginate-di-aldehyde (ADA) and gelatin (GEL), was used to fabricate 3D printed grid-like structures for cartilage tissue engineering. Enzymatic and ionic crosslinking techniques using microbial transglutaminase (mTG) and divalent ions (CaCl) were combined to ensure long-term stability of the 3D printed structures. Human nasoseptal chondrocytes were embedded in ADA-GEL prior to 3D printing. Cell viability, proliferation, and metabolic activity were analyzed after 7 and 14 days. The influence of the enzymatic crosslinking and the 3D printing process on the primary human chondrocytes were investigated. It was found that neither the 3D printing process nor the crosslinking by mTG impaired chondrocyte viability. The formation of the main cartilage-specific extracellular matrix components collagen type II and cartilage proteoglycans was shown by immunohistochemical staining. The combination of enzymatic and ionic crosslinking for the 3D printing of ADA-GEL hydrogels is therefore a promising approach for the 3D cultivation of primary human chondrocytes for cartilage tissue engineering.
由于软骨是人体中少数没有血管化的组织之一,人体修复软骨缺损的能力非常有限。因此,需要新型的促进植入软骨细胞形成软骨的生物材料。在这项工作中,使用氧化海藻酸钠-明胶水凝胶系统,即海藻酸二醛(ADA)和明胶(GEL),来制造用于软骨组织工程的3D打印网格状结构。结合使用微生物转谷氨酰胺酶(mTG)和二价离子(CaCl)的酶促交联和离子交联技术,以确保3D打印结构的长期稳定性。在3D打印之前,将人鼻中隔软骨细胞嵌入ADA-GEL中。在7天和14天后分析细胞活力、增殖和代谢活性。研究了酶促交联和3D打印过程对原代人软骨细胞的影响。发现3D打印过程和mTG交联均未损害软骨细胞活力。免疫组织化学染色显示了主要的软骨特异性细胞外基质成分II型胶原蛋白和软骨蛋白聚糖的形成。因此,用于ADA-GEL水凝胶3D打印的酶促交联和离子交联组合是用于软骨组织工程的原代人软骨细胞3D培养的一种有前途的方法。