Parker H. Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, Georgia 30332-0363, USA.
Tissue Eng Part A. 2013 Feb;19(3-4):475-83. doi: 10.1089/ten.TEA.2012.0125. Epub 2012 Oct 10.
The goal of this study was to determine the effects of chondrogenic predifferentiation on the ability of bone marrow-derived stromal cells (BMSCs) delivered to growth plate defects to restore growth function. Chondrogenesis was induced with transforming growth factor (TGF)-β1 treatment in high-density monolayer cultures of BMSCs in vitro. The predifferentiated or undifferentiated BMSCs were either seeded into agarose gels for continued in vitro culture, or injected into growth plate defects via an in situ gelling agarose. Predifferentiated BMSCs had higher Sox-9, type II collagen, and aggrecan mRNA levels compared to undifferentiated cells after high-density monolayer culture. After transfer to agarose gels, predifferentiated cells did not produce a cartilaginous matrix, even with continued TGF-β1 stimulation, whereas undifferentiated cells produced a cartilaginous matrix in this system. Three-dimensional images of the growth plate created from microcomputed tomography scans showed that delivery of either predifferentiated or undifferentiated cells to defects resulted in a decrease in mineralized tether formation (fusion) in the growth plate tissue surrounding the defect to normal levels. Limb length discrepancy between injured and control limbs was corrected after treatment with undifferentiated, but not predifferentiated, cells. These results indicate that cell therapy may be an effective treatment to reduce growth dysfunction after growth plate injury, perhaps by maintaining the health of the uninjured growth plate tissue, and that the cell differentiation state plays a role in restoring the growth potential of the injured limb.
本研究旨在确定软骨分化前体对骨髓基质细胞(BMSCs)向生长板缺损部位移植后恢复生长功能能力的影响。在体外高浓度单层培养的 BMSCs 中,用转化生长因子(TGF)-β1 处理诱导软骨生成。将预分化或未分化的 BMSCs 接种到琼脂糖凝胶中进行体外培养,或通过原位凝胶化琼脂糖注射到生长板缺损部位。与未分化细胞相比,高浓度单层培养后的预分化 BMSCs 的 Sox-9、II 型胶原和聚集蛋白聚糖 mRNA 水平更高。转至琼脂糖凝胶后,即使继续用 TGF-β1 刺激,预分化细胞也不会产生软骨基质,而未分化细胞在该系统中会产生软骨基质。来自微计算机断层扫描的生长板三维图像显示,将预分化或未分化细胞递送到缺损部位会导致缺损周围生长板组织中矿化栓形成(融合)减少至正常水平。在用未分化细胞而不是预分化细胞治疗后,受伤和对照肢体之间的肢体长度差异得到纠正。这些结果表明,细胞治疗可能是一种有效治疗方法,可以减少生长板损伤后的生长功能障碍,可能通过维持未受伤生长板组织的健康,以及细胞分化状态在恢复受损肢体的生长潜力方面发挥作用。