Hidaka C, Quitoriano M, Warren R F, Crystal R G
Division of Pulmonary and Critical Care Medicine, Weill Medical College of Cornell University, New York, NY, USA.
J Orthop Res. 2001 Sep;19(5):751-8. doi: 10.1016/S0736-0266(01)00019-5.
Bone morphogenic protein-7 (BMP-7) supports ectopic cartilage and bone formation, is expressed in normal articular cartilage, and increases matrix synthesis in chondrocytes. Based on this knowledge, we hypothesized that an adenovirus (Ad) vector encoding human BMP-7 could be used to modify chondrocytes genetically to improve their capacity for cartilage repair. An adenovirus vector encoding BMP-7 (AdBMP-7) was constructed and its bioactivity confirmed by ectopic bone formation assay. AdBMP-7 modification of bovine chondrocytes induced expression of BMP-7 mRNA and bioactive protein, resulting in an increase in incorporation of 35SO4- into proteoglycan, 3H-proline uptake into protein, and the expression of the cartilage-specific matrix genes, aggrecan and type II collagen. An in vitro model of chondrocyte transplantation was used to demonstrate the feasibility of using genetically modified chondrocytes to enhance formation of cartilage-like tissue. When transplanted onto cartilage explants and maintained in vitro for 3 weeks, chondrocytes modified with AdBMP-7 formed 1.9-fold thicker tissue than chondrocytes modified with a control vector (P < 0.001). This tissue was positive for type II collagen and proteoglycan but negative for type X collagen and demonstrated a cartilage-like morphology. These observations suggest that Ad-mediated transfer of BMP-7 gene to chondrocytes enhances the chondrocyte-specific matrix synthesis and their capacity to form cartilage-like tissue, thus representing a strategy that may improve cell-based cartilage repair.
骨形态发生蛋白-7(BMP-7)可促进异位软骨和骨形成,在正常关节软骨中表达,并能增加软骨细胞中的基质合成。基于这一认识,我们推测编码人BMP-7的腺病毒(Ad)载体可用于对软骨细胞进行基因改造,以提高其软骨修复能力。构建了编码BMP-7的腺病毒载体(AdBMP-7),并通过异位骨形成试验证实了其生物活性。用AdBMP-7对牛软骨细胞进行改造可诱导BMP-7 mRNA和生物活性蛋白的表达,导致35SO4-掺入蛋白聚糖增加、3H-脯氨酸摄取到蛋白质中增加,以及软骨特异性基质基因聚集蛋白聚糖和II型胶原的表达增加。利用软骨细胞移植的体外模型来证明使用基因改造的软骨细胞增强类软骨组织形成的可行性。当将用AdBMP-7改造的软骨细胞移植到软骨外植体上并在体外培养3周时,其形成的组织比用对照载体改造的软骨细胞厚1.9倍(P<0.001)。该组织II型胶原和蛋白聚糖呈阳性,但X型胶原呈阴性,并呈现出类软骨形态。这些观察结果表明,Ad介导的BMP-7基因向软骨细胞的转移增强了软骨细胞特异性基质合成及其形成类软骨组织的能力,从而代表了一种可能改善基于细胞的软骨修复的策略。