Pentosan Polysulfate Sodium Restores the Phenotype of Dedifferentiated Monolayer Canine Articular Chondrocytes Cultured in Alginate Beads

Eugene C. Bwalya, Sangho Kim, Jing Fang, H. S. Wijekoon, K. Hosoya, M. Okumura
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引用次数: 1

Abstract

Autologous chondrocyte transplantation is a promising option for the repair of isolated osteoarthritic cartilage lesions that requires isolation and expansion of chondrocytes from a small cartilage biopsy prior to implantation. However, when cultured in vitro, chondrocytes lose their stable phenotype and dedifferentiate to fibroblastic-like cells. The study investigated the potential of pentosan polysulfate (PPS) sodium to restore the phenotype of dedifferentiated monolayer articular chondrocytes. Canine articular chondrocytes isolated from four cartilage samples were culture expanded to establish primary culture. First passage chondrocytes were cultured as alginate beads for 18 days under normoxia in PPS concentrations of 0, 1, 5, 15 and 40 μg/mL in 20% DMEM. Effect of PPS on type I, II and X collagen, aggrecan and Runx2 gene expression were evaluated by real-time PCR. Runx2, HIF-1α and HIF-2α protein expression were evaluated by Western blot and proteoglycan deposition was determined by Alcian blue stain. Dedifferentiated chondrocytes fully retained their phenotype as evidenced by increased synthesis of cartilage-specific genes, type II collagen and aggrecan mRNA with complete suppression of type I and X collagen at PPS concentrations of 15 and 40 μg/mL. Compared to the control, type II collagen and aggrecan mRNA were significantly upregulated (P<0.05) at 5, 15 and 40 μg/mL and 5 and 15 μg/mL PPS, respectively. PPS significantly enhanced proteoglycan with peak deposition at 5 μg/mL compared to control. HIF-1α and HIF-2α proteins were detectable at protein level for the first time under normoxia condition in alginate culture. The study demonstrates for the first time the restoration of dedifferentiated canine articular chondrocytes phenotype by combining alginate encapsulation with culture in PPS without the addition of known chondrocytic growth factors. The study confirms PPS as novel chondroinductive factor with potential to offer a solution to the major challenges that exist in cartilage tissue engineering.
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戊聚糖聚硫酸钠恢复藻酸盐珠培养的去分化单层犬关节软骨细胞的表型
自体软骨细胞移植是修复孤立性骨关节炎软骨病变的一个很有前途的选择,需要在植入前从小软骨活检中分离和扩增软骨细胞。然而,当体外培养时,软骨细胞失去其稳定的表型并去分化为成纤维细胞样细胞。本研究探讨了戊聚糖聚硫酸钠(PPS)恢复去分化单层关节软骨细胞表型的潜力。从四个软骨样本中分离的犬关节软骨细胞进行扩增培养,建立原代培养。将首代软骨细胞培养成海藻酸盐珠状细胞,在20% DMEM中,PPS浓度分别为0、1、5、15和40 μg/mL,在常氧条件下培养18 d。实时荧光定量PCR检测PPS对I、II、X型胶原蛋白、聚集蛋白及Runx2基因表达的影响。Western blot检测Runx2、HIF-1α和HIF-2α蛋白表达,Alcian blue染色检测蛋白多糖沉积。当PPS浓度为15和40 μg/mL时,软骨特异性基因、II型胶原蛋白和聚集蛋白mRNA的合成增加,I型和X型胶原蛋白的合成完全抑制,去分化软骨细胞完全保留了其表型。与对照组相比,在5、15、40 μg/mL和5、15 μg/mL PPS浓度下,ⅱ型胶原和聚集蛋白mRNA均显著上调(P<0.05)。与对照组相比,PPS显著增强蛋白多糖,在5 μg/mL时达到峰值沉积。在褐藻酸盐培养条件下,首次在蛋白水平上检测到HIF-1α和HIF-2α蛋白。本研究首次证明了在不添加已知软骨细胞生长因子的情况下,海藻酸盐包埋与PPS培养相结合可以恢复去分化的犬关节软骨细胞表型。该研究证实PPS是一种新型的软骨诱导因子,有可能为软骨组织工程中存在的主要挑战提供解决方案。
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