Meng Du, Liu Rui, Pei Li, Hou Lei, Ning Qian, Yu Qing, Feng Lu, Zhao Xinhan
Department of Oncology, First Affiliated Hospital of Medical School of Xi'an Jiaotong University, Xi'an, Shaanxi 710061, P.R. China.
Mol Med Rep. 2015 Apr;11(4):2555-61. doi: 10.3892/mmr.2014.3043. Epub 2014 Dec 3.
The aim of the present study was to investigate the feasibility of lentiviral‑mediated Cys‑Asn‑Gly‑Arg‑Cys (CNGRC) peptide gene transduction in adipose stem cells. Adipose stem cells were prepared using enzymatic digestion and repeated adherence methods and identified in culture by immunofluorescence staining of surface markers. The pluripotency of the cultured adipose stem cells was confirmed by their induced differentiation into bone and fat cells. Following polymerase chain reaction amplification, the gene sequence for the CNGRC peptide was cloned into a lentiviral vector, which was then co‑transfected into 293T cells with packaging plasmids Helper 1.0 and Helper 2.0. The lentiviruses carrying the CNGRC peptide gene were then harvested and used to transfect adipose stem cells. Following transduction, expression of CNGRC in adipose stem cells was detected using western blot analysis. Adipose stem cells in culture were successfully induced to differentiate into adipocytes and osteoblasts and the lentiviral vector containing CNGRC‑3Flag‑EGFP was successfully constructed. Following transduction, western blot analysis and immunofluorescence staining demonstrated expression of the CNGRC protein in adipose stem cells. This suggested that adipose stem cell lines expressing the CNGRC peptide were successfully established.
本研究的目的是探讨慢病毒介导的半胱氨酸-天冬酰胺-甘氨酸-精氨酸-半胱氨酸(CNGRC)肽基因转导至脂肪干细胞中的可行性。采用酶消化和反复贴壁法制备脂肪干细胞,并通过表面标志物的免疫荧光染色在培养中进行鉴定。通过诱导培养的脂肪干细胞分化为骨细胞和脂肪细胞来确认其多能性。经过聚合酶链反应扩增后,将CNGRC肽的基因序列克隆到慢病毒载体中,然后与包装质粒Helper 1.0和Helper 2.0共转染至293T细胞中。随后收获携带CNGRC肽基因的慢病毒并用于转染脂肪干细胞。转导后,使用蛋白质印迹分析检测脂肪干细胞中CNGRC的表达。培养的脂肪干细胞成功诱导分化为脂肪细胞和成骨细胞,并且成功构建了含有CNGRC-3Flag-EGFP的慢病毒载体。转导后,蛋白质印迹分析和免疫荧光染色证明脂肪干细胞中CNGRC蛋白的表达。这表明成功建立了表达CNGRC肽的脂肪干细胞系。