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Effect of Biphasic Calcium Phosphate Treated with Vascular Endothelial Growth Factor on Osteogenesis and Angiogenesis Gene Expression In Vitro

机译:血管内皮生长因子对血管内皮生长因子对骨质发生及体外血管生成基因表达的影响

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Biodegradable biphasic calcium phosphate (BCP) scaffold holds tremendous potential for bone tissue engineering. It elicits response from cells such as endothelial cells (ECs) that are similar to those elicited by bone. ECs promote bone regeneration by stimulating both neovascularisation and osteogenesis. For an effective coupling of angiogenesis and osteogenesis, vascular endothelial growth factor (VEGF) is required. The aim of this work is to study the effectiveness of VEGF-added-BCP on the expression of osteogenesis and angiogenesis genes in ECs. Commercially obtained rat aortic ECs were cultured in the endothelial-cell growth medium. The cells were treated with three different modalities: BCP- only, VEGF- only, and VEGF-added-BCP. The optimal BCP and VEGF concentrations were determined. The cells were harvested at four different time intervals (day 3, day 7, day 10 and day 14) and were subjected to RNA isolation using RNA extraction kit (analytikjena, Germany). This was followed by performing reverse transcriptase-PCR (RT-PCR) (Qiagen, Germany) to amplify the osteogenesis and angiogenesis-regulated genes. The RT-PCR products were then electrophoresed. The gel image was captured using Image Analyser. Suitable concentration of BCP was 10mg/ml while optimal VEGF was 15ng/ml. Angiogenesis and osteogenesis genes were clearly expressed in ECs in response to treatments. Angiogenesis gene (VEGF) was highly expressed by VEGF-only treatment but showed some changes with added BCP. Osteogenesis genes (BMP-2, ALP, OC and OPN) were shown to be positively affected by both BCP and VEGF. Some genes were expressed at an earlier time interval compared to the other genes depending on the type of treatments. BCP-only treatment induced high expression of early regulating osteogenesis genes (BMP-2 and OPN). Mineralized gene markers (ALP and OC) were however, highly expressed with VEGF-added-BCP treatment. Combination of BCP and VEGF modality on ECs was suggested to initiate osteogenesis and angiogenesis related gene expressions earlier than the other modalities.
机译:可生物降解的双相磷酸钙(BCP)支架对骨组织工程具有巨大的潜力。它引发了与骨引起的那些类似的内皮细胞(ECS)的细胞的响应。 ECS通过刺激新生血管和骨质发生来促进骨再生。对于血管生成和骨肉发生的有效耦合,需要血管内皮生长因子(VEGF)。这项工作的目的是研究VEGF加入BCP对ECS中骨发生和血管生成基因表达的有效性。商业化的大鼠主动脉EC在内皮细胞生长培养基中培养。用三种不同的方式处理细胞:仅限BCP-ock,VEGF和VEGF-加入BCP。确定最佳的BCP和VEGF浓度。将细胞以四种不同的时间间隔(第3天,第7天,第10天和第14天)收获,并使用RNA提取试剂盒(Analytikjena,德国)进行RNA分离。随后进行逆转录酶-PCR(RT-PCR)(Qiagen,德国)以扩增骨开发和血管生成调节基因。然后将RT-PCR产物电泳。使用图像分析仪捕获凝胶图像。合适的BCP浓度为10mg / ml,而最佳VEGF为15ng / ml。抗血管生成和成骨基因在ECS中清楚地表达响应治疗。血管生成基因(VEGF)高度表达VEGF的处理,但随着添加的BCP而显示一些变化。显示成骨基因(BMP-2,ALP,OC和OPN)被BCP和VEGF的阳性受到影响。与其他基因相比,一些基因以较早的时间间隔表达,这取决于治疗的类型。仅BCP治疗诱导早期调节成骨发生基因的高表达(BMP-2和OPN)。然而,矿化基因标记物(ALP和OC)对VEGF加入-BCP处理具有高表达。 BCP和VEGF模态对ECS的组合提出了比其他方式更早的骨发生和血管生成相关基因表达。

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