Matsushima Asako, Kotobuki Noriko, Tadokoro Mika, Kawate Kenji, Yajima Hiroshi, Takakura Yoshinori, Ohgushi Hajime
Research Institute for Cell Engineering (RICE), National Institute of Advanced Industrial Science and Technology (AIST), Amagasaki, Hyogo, Japan.
Artif Organs. 2009 Jun;33(6):474-81. doi: 10.1111/j.1525-1594.2009.00749.x.
The aim of the current study was to examine in vitro osteogenic capability and in vivo bone formation of mesenchymal stromal cells (MSCs) on two kinds of calcium phosphate ceramics. MSCs derived from human bone marrow were seeded on either hydroxyapatite (HA) ceramic or beta-tricalcium phosphate (beta-TCP) ceramic and then cultured in a medium supplemented with a donor's serum, vitamin C, beta-glycerophosphate, and dexamethasone. The culture revealed the expression of alkaline phosphatase activity, indicating the osteogenic differentiation of the MSCs on the ceramics (fabrication of tissue-engineered construct). The constructs were then implanted subcutaneously into nude rats for 8 weeks. New bone formation was observed in both types of ceramics, and human-specific Alu sequence was detected by in situ hybridization analysis. Quantitative microcomputed tomography showed that the volume of the new bone in the HA ceramic was greater than that in the beta-TCP ceramic in six of seven cases. These results suggest that human MSCs cultured on ceramics could retain their osteogenic capability even after ectopic implantation and provide a rationale for the use of tissue-engineered constructs derived from a patient's MSCs and calcium phosphate ceramics in bone tissue regeneration.
本研究的目的是检测间充质基质细胞(MSCs)在两种磷酸钙陶瓷上的体外成骨能力和体内骨形成情况。将源自人骨髓的MSCs接种到羟基磷灰石(HA)陶瓷或β-磷酸三钙(β-TCP)陶瓷上,然后在补充有供体血清、维生素C、β-甘油磷酸酯和地塞米松的培养基中培养。培养显示出碱性磷酸酶活性的表达,表明MSCs在陶瓷上发生了成骨分化(组织工程构建体的制备)。然后将构建体皮下植入裸鼠体内8周。在两种类型的陶瓷中均观察到新骨形成,并通过原位杂交分析检测到人类特异性Alu序列。定量微计算机断层扫描显示,在7例中的6例中,HA陶瓷中新骨的体积大于β-TCP陶瓷中的新骨体积。这些结果表明,在陶瓷上培养的人MSCs即使在异位植入后仍能保持其成骨能力,并为使用源自患者MSCs和磷酸钙陶瓷的组织工程构建体进行骨组织再生提供了理论依据。