Schildberg Theresa, Rauh Juliane, Bretschneider Henriette, Stiehler Maik
University Centre for Orthopaedics & Trauma Surgery and Centre for Translational Bone, Joint & Soft Tissue Research, University Hospital Carl Gustav Carus at the Technische Universität Dresden, Dresden, Germany.
Stem Cell Res. 2013 Nov;11(3):1288-98. doi: 10.1016/j.scr.2013.08.015. Epub 2013 Sep 9.
Bone marrow stromal cells (BMSCs) are key cellular components for musculoskeletal tissue engineering strategies. Furthermore, recent data suggest that BMSCs are involved in the development of Osteoarthritis (OA) being a frequently occurring degenerative joint disease. Reliable reference genes for the molecular evaluation of BMSCs derived from donors exhibiting OA as a primary co-morbidity have not been reported on yet. Hence, the aim of the study was to identify reference genes suitable for comparative gene expression analyses using OA-BMSCs. Passage 1 bone marrow derived BMSCs were isolated from n=13 patients with advanced stage idiopathic hip osteoarthritis and n=15 age-matched healthy donors. The expression of 31 putative reference genes was analyzed by quantitative reverse transcription polymerase chain reaction (qRT-PCR) using a commercially available TaqMan(®) assay. Calculating the coefficient of variation (CV), mRNA expression stability was determined and afterwards validated using geNorm and NormFinder algorithms. Importin 8 (IPO8), TATA box binding protein (TBP), and cancer susceptibility candidate 3 (CASC3) were identified as the most stable reference genes. Notably, commonly used reference genes, e.g. beta-actin (ACTB) and beta-2-microglobulin (B2M) were among the most unstable genes. For normalization of gene expression data of OA-BMSCs the combined use of IPO8, TBP, and CASC3 gene is recommended.
骨髓基质细胞(BMSCs)是肌肉骨骼组织工程策略的关键细胞成分。此外,最近的数据表明,BMSCs参与了骨关节炎(OA)的发展,骨关节炎是一种常见的退行性关节疾病。对于以OA作为主要合并症的供体来源的BMSCs进行分子评估的可靠参考基因尚未见报道。因此,本研究的目的是鉴定适用于使用OA-BMSCs进行比较基因表达分析的参考基因。从13例晚期特发性髋骨关节炎患者和15例年龄匹配的健康供体中分离出第1代骨髓来源的BMSCs。使用市售的TaqMan®检测试剂盒,通过定量逆转录聚合酶链反应(qRT-PCR)分析31个假定参考基因的表达。计算变异系数(CV),确定mRNA表达稳定性,然后使用geNorm和NormFinder算法进行验证。输入蛋白8(IPO8)、TATA盒结合蛋白(TBP)和癌症易感性候选基因3(CASC3)被确定为最稳定的参考基因。值得注意的是,常用的参考基因,如β-肌动蛋白(ACTB)和β-2-微球蛋白(B2M)是最不稳定的基因之一。对于OA-BMSCs基因表达数据的标准化,建议联合使用IPO8、TBP和CASC3基因。