Xiao Hai-bo, Mei Ju, Zhang Bao-ren, Huang Sheng-dong
Department of Thoracic and Cardiovascular Surgery, Changhai Hospital, Second Military Medical University, Shanghai 200433, China.
Zhonghua Wai Ke Za Zhi. 2005 Jan 15;43(2):92-6.
To study transcription, expression, and bioactivity of expressive protein of vascular endothelial growth factor 165 (VEGF(165)) gene, after bone marrow stromal cells (BMSCs) were transferred by VEGF(165) gene mediated by adenovirus vector ex vivo.
BMSCs were Isolated and cultured by gradient centrifugation method. The cells cultured are transferred by recombinant adenovirus vector that carry VEGF(165) gene. Transcription and expression of VEGF(165) gene in BMSCs and secretion of VEGF protein in culture medium were measured by reverse transcriptase-polymerase chain reaction (RT-PCR), Western blot and enzyme linked immunosorbent assay (ELISA) methods. The activity of VEGF protein in culture media was detected by proliferation effects on vascular endothelial cells.
When Ad. VEGF(165) transferred into BMSCs, there was an effective transcription and expression. The expressed product in the media of transferred cells had highly biological activity on proliferation of rat aortic vascular endothelial cells (P < 0.01).
Adenovirus vector can be transferred into BMSCs efficiently and safely. Adenovirus mediated VEGF(165) gene transferred into BMSCs could express VEGF protein with highly biological activity, which provided foundation on BMSCs based gene therapy for ischemic disease.
研究经腺病毒载体介导血管内皮生长因子165(VEGF(165))基因体外转染骨髓基质细胞(BMSCs)后,VEGF(165)基因的转录、表达及表达蛋白的生物活性。
采用梯度离心法分离培养BMSCs。用携带VEGF(165)基因的重组腺病毒载体转染培养的细胞。采用逆转录-聚合酶链反应(RT-PCR)、蛋白质印迹法和酶联免疫吸附测定(ELISA)法检测BMSCs中VEGF(165)基因的转录和表达以及培养基中VEGF蛋白的分泌情况。通过对血管内皮细胞的增殖作用检测培养基中VEGF蛋白的活性。
当Ad.VEGF(165)转染至BMSCs时,有有效的转录和表达。转染细胞培养基中的表达产物对大鼠主动脉血管内皮细胞的增殖具有高度生物活性(P < 0.01)。
腺病毒载体可高效、安全地转染至BMSCs。腺病毒介导VEGF(165)基因转染至BMSCs可表达具有高度生物活性的VEGF蛋白,为基于BMSCs的缺血性疾病基因治疗提供了基础。