Ogawa Rei, Mizuno Shuichi, Murphy George F, Orgill Dennis P
Division of Plastic Surgery, Department of Surgery, Harvard Medical School, Brigham and Women's Hospital, Boston, Massachusetts 02115, USA.
Tissue Eng Part A. 2009 Oct;15(10):2937-45. doi: 10.1089/ten.TEA.2008.0672.
The optimal production of three-dimensional cartilage in vitro requires both inductive factors and specified culture conditions (e.g., hydrostatic pressure [HP], gas concentration, and nutrient supply) to promote cell viability and maintain phenotype. In this study, we optimized the conditions for human cartilage induction using human adipose-derived stem cells (ASCs), collagen scaffolds, and cyclic HP treatment.
Human ASCs underwent primary culture and three passages before being seeded into collagen scaffolds. These constructs were incubated for 1 week in an automated bioreactor using cyclic HP at 0-0.5 MPa, 0.5 Hz, and compared to constructs exposed to atmospheric pressure. In both groups, chondrogenic differentiation medium including transforming growth factor-beta1 was employed. One, 2, 3, and 4 weeks after incubation, the cell constructs were harvested for histological, immunohistochemical, and gene expression evaluation.
In histological and immunohistochemical analyzes, pericellular and extracellular metachromatic matrix was observed in both groups and increased over 4 weeks, but accumulated at a higher rate in the HP group. Cell number was maintained in the HP group over 4 weeks but decreased after 2 weeks in the atmospheric pressure group. Chondrogenic-specific gene expression of type II and X collagen, aggrecan, and SRY-box9 was increased in the HP group especially after 2 weeks.
Our results demonstrate chondrogenic differentiation of ASCs in a three-dimensional collagen scaffolds with treatment of a cyclic HP. Cyclic HP was effective in enhancing accumulation of extracellular matrix and expression of genes indicative of chondrogenic differentiation.
体外三维软骨的最佳生成需要诱导因子和特定的培养条件(如流体静压[HP]、气体浓度和营养供应)来促进细胞活力并维持表型。在本研究中,我们使用人脂肪来源干细胞(ASC)、胶原蛋白支架和循环HP处理优化了人软骨诱导的条件。
人ASC进行原代培养并传代三次,然后接种到胶原蛋白支架中。这些构建体在自动生物反应器中使用0 - 0.5 MPa、0.5 Hz的循环HP孵育1周,并与暴露于大气压的构建体进行比较。两组均采用包含转化生长因子-β1的软骨形成分化培养基。孵育1、2、3和4周后,收获细胞构建体进行组织学、免疫组织化学和基因表达评估。
在组织学和免疫组织化学分析中,两组均观察到细胞内和细胞外异染基质,且在4周内增加,但在HP组中积累速率更高。HP组在4周内细胞数量保持稳定,而大气压组在2周后细胞数量减少。HP组中II型和X型胶原蛋白、聚集蛋白聚糖和SRY盒9的软骨形成特异性基因表达增加,尤其是在2周后。
我们的结果表明,在循环HP处理下,ASC在三维胶原蛋白支架中发生软骨形成分化。循环HP有效地增强了细胞外基质的积累和软骨形成分化相关基因的表达。