Jin Guang-Zhen, Kim Hae-Won
1Institute of Tissue Regeneration Engineering (ITREN), Dankook University, 119 Dandae-ro, Dongnam-gu, Cheonan, 31116 Korea.
2Department of Nanobiomedical Science & BK21 PLUS NBM Global Research Center for Regenerative Medicine, Dankook University, Cheonan, Korea.
Tissue Eng Regen Med. 2016 Jun 9;13(3):235-241. doi: 10.1007/s13770-016-0038-6. eCollection 2016 Jun.
Cartilage repair is substantially intractable due to poor self-healing ability. Porous microspheres can be a fascinating three-dimensional matrix for cell culture and injectable carrier in cartilage engineering. In this study, we assessed the feasible use of porous biopolymer microspheres for chondrocyte carriers. When seeded onto the blended biopolymer microspheres and followed by a dynamic spinner flask culture, the chondrocytes showed robust growth behaviors during the culture period. The gene expressions of , type II collagen, and aggrecan were significantly upregulated after 2-week of culture. Furthermore, immunolocalization of type II collagen and secretion of glycosaminolglycan became prominent. The results suggest the feasible usefulness of the porous microspheres as the cell culture matrix and the subsequent delivery into cartilage defects.
由于自我修复能力较差,软骨修复极具挑战性。多孔微球可成为软骨工程中用于细胞培养的极具吸引力的三维基质和可注射载体。在本研究中,我们评估了多孔生物聚合物微球作为软骨细胞载体的可行性。当接种到混合生物聚合物微球上并随后进行动态转瓶培养时,软骨细胞在培养期间表现出强劲的生长行为。培养2周后,Ⅱ型胶原蛋白和聚集蛋白聚糖的基因表达显著上调。此外,Ⅱ型胶原蛋白的免疫定位和糖胺聚糖的分泌变得明显。结果表明多孔微球作为细胞培养基质以及随后用于软骨缺损的递送具有可行性。