Huang A H, Yeger-McKeever M, Stein A, Mauck R L
McKay Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, University of Pennsylvania, Philadelphia, PA 19104, United States.
Osteoarthritis Cartilage. 2008 Sep;16(9):1074-82. doi: 10.1016/j.joca.2008.02.005. Epub 2008 Mar 18.
The objective of this study was to determine the capacity of chondrocyte- and mesenchymal stem cell (MSC)-laden hydrogel constructs to achieve native tissue tensile properties when cultured in a chemically defined medium supplemented with transforming growth factor-beta3 (TGF-beta3).
Cell-laden agarose hydrogel constructs (seeded with bovine chondrocytes or MSCs) were formed as prismatic strips and cultured in a chemically defined serum-free medium in the presence or absence of TGF-beta3. The effects of seeding density (10 vs 30 million cells/mL) and cell type (chondrocyte vs MSC) were evaluated over a 56-day period. Biochemical content, collagenous matrix deposition and localization, and tensile properties (ramp modulus, ultimate strain, and toughness) were assessed biweekly.
Results show that the tensile properties of cell-seeded agarose constructs increase with time in culture. However, tensile properties (modulus, ultimate strain, and toughness) achieved on day 56 were not dependent on either the initial seeding density or the cell type employed. When cultured in medium supplemented with TGF-beta3, tensile modulus increased and plateaued at a level of 300-400 kPa for each cell type and starting cell concentration. Ultimate strain and toughness also increased relative to starting values. Collagen deposition increased in constructs seeded with both cell types and at both seeding densities, with exposure to TGF-beta3 resulting in a clear shift toward type II collagen deposition as determined by immunohistochemical staining.
These findings demonstrate that the tensile properties, an important and often overlooked metric of cartilage development, increase with time in culture in engineered hydrogel-based cartilage constructs. Under the free-swelling conditions employed in the present study, tensile moduli and toughness did not match that of the native tissue, though significant time-dependent increases were observed with the inclusion of TGF-beta3. Of note, MSC-seeded constructs achieved tensile properties that were comparable to chondrocyte-seeded constructs, confirming the utility of this alternative cell source in cartilage tissue engineering. Further work, including both modulation of the chemical and mechanical culture environment, is required to optimize the deposition of collagen and its remodeling to achieve tensile properties in engineered constructs matching the native tissue.
本研究的目的是确定负载软骨细胞和间充质干细胞(MSC)的水凝胶构建体在添加转化生长因子-β3(TGF-β3)的化学成分明确的培养基中培养时,达到天然组织拉伸性能的能力。
将负载细胞的琼脂糖水凝胶构建体(接种牛软骨细胞或间充质干细胞)制成棱柱形条带,并在有无TGF-β3的情况下,在化学成分明确的无血清培养基中培养。在56天的时间内评估接种密度(1000万与3000万个细胞/毫升)和细胞类型(软骨细胞与间充质干细胞)的影响。每两周评估生化成分、胶原基质沉积和定位以及拉伸性能(斜坡模量、极限应变和韧性)。
结果表明,接种细胞的琼脂糖构建体的拉伸性能随培养时间增加。然而,在第56天达到的拉伸性能(模量、极限应变和韧性)并不取决于初始接种密度或所用的细胞类型。当在添加TGF-β3的培养基中培养时,每种细胞类型和起始细胞浓度的拉伸模量都会增加并稳定在300 - 至400 kPa的水平。极限应变和韧性也相对于起始值增加。两种细胞类型和两种接种密度接种的构建体中胶原沉积均增加,免疫组织化学染色显示,暴露于TGF-β3会导致明显向II型胶原沉积转变。
这些发现表明,拉伸性能是软骨发育中一个重要且常被忽视的指标,在基于水凝胶的工程软骨构建体中,其随培养时间增加。在本研究采用的自由膨胀条件下,拉伸模量和韧性与天然组织不匹配,不过加入TGF-β3后观察到显著的时间依赖性增加。值得注意的是,接种间充质干细胞的构建体达到的拉伸性能与接种软骨细胞的构建体相当,证实了这种替代细胞来源在软骨组织工程中的实用性。需要进一步开展工作,包括调节化学和机械培养环境,以优化胶原的沉积及其重塑,从而在工程构建体中实现与天然组织匹配的拉伸性能。