Yamasaki Takuma, Deie Masataka, Shinomiya Rikuo, Izuta Yasunori, Yasunaga Yuji, Yanada Shinobu, Sharman Patrick, Ochi Mitsuo
Department of Orthopaedic Surgery, Graduate School of Biomedical Sciences, Hiroshima University, 1-2-3, Kasumi, Minami-ku, Hiroshima, 734-8551, Japan.
J Biomed Mater Res A. 2005 Oct 1;75(1):23-30. doi: 10.1002/jbm.a.30369.
The purpose of this study was to regenerate a meniscus using a scaffold from a normal meniscus and mesenchymal stromal cells derived from bone marrow (BM-MSCs). Thirty Sprague-Dawley rat menisci were excised and freeze-thawed three times with liquid nitrogen to kill the original meniscal cells. Bone marrow was aspirated from enhanced green fluorescent protein transgenic Sprague-Dawley rats. BM-MSCs were isolated, cultured for 2 weeks, and 2 x 10(5) cells were then seeded onto the meniscal scaffolds. Using a fluorescent microscope and immunohistochemical staining, repopulation of enhanced green fluorescent protein positive cells was observed in the superficial zone of the scaffold after 1 week of culture, and then in the deep zone after 2 weeks. At 4 weeks, expression of extracellular matrices was detected histologically and expression of mRNA for aggrecan and type X collagen was detected. Stiffness of the cultured tissue, assessed by the indentation stiffness test, had increased significantly after 2 weeks in culture, and approximated the stiffness of a normal meniscus. From this study, we conclude that a scaffold derived from a normal meniscus seeded with BM-MSCs can form a meniscus approximating a normal meniscus.
本研究的目的是使用来自正常半月板的支架和源自骨髓的间充质基质细胞(BM-MSCs)来再生半月板。切除30个Sprague-Dawley大鼠半月板,并用液氮冻融三次以杀死原有的半月板细胞。从增强型绿色荧光蛋白转基因Sprague-Dawley大鼠中抽取骨髓。分离BM-MSCs,培养2周,然后将2×10⁵个细胞接种到半月板支架上。使用荧光显微镜和免疫组织化学染色,培养1周后在支架的表层观察到增强型绿色荧光蛋白阳性细胞的重新填充,2周后在深层观察到。在4周时,通过组织学检测细胞外基质的表达,并检测聚集蛋白聚糖和X型胶原的mRNA表达。通过压痕硬度测试评估,培养组织的硬度在培养2周后显著增加,并接近正常半月板的硬度。从本研究中,我们得出结论,接种BM-MSCs的来自正常半月板的支架可以形成接近正常半月板的半月板。