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Mild Heat Stress Enhances Angiogenesis in a Co-culture System Consisting of Primary Human Osteoblasts and Outgrowth Endothelial Cells

机译:轻度的热应激增强了由原代人成骨细胞和内皮生长细胞组成的共培养系统中的血管生成

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摘要

The repair and regeneration of large bone defects, including the formation of functional vasculature, represents a highly challenging task for tissue engineering and regenerative medicine. Recent studies have shown that vascularization and ossification can be stimulated by mild heat stress (MHS), which would offer the option to enhance the bone regeneration process by relatively simple means. However, the mechanisms of MHS-enhanced angiogenesis and osteogenesis, as well as potential risks for the treated cells are unclear. We have investigated the direct effect of MHS on angiogenesis and osteogenesis in a co-culture system of human outgrowth endothelial cells (OECs) and primary osteoblasts (pOBs), and assessed cytotoxic effects, as well as the levels of various heat shock proteins (HSPs) synthesized under these conditions. Enhanced formation of microvessel-like structures was observed in co-cultures exposed to MHS (41°C, 1 h), twice per week, over a time period of 7–14 days. As shown by real-time polymerase chain reaction (PCR), the expression of vascular endothelial growth factor (VEGF), angiopoietin-1 (Ang-1), angiopoietin-2 (Ang-2), and tumor necrosis factor-alpha was up-regulated in MHS-treated co-cultures 24 h post-treatment. At the protein level, significantly elevated VEGF and Ang-1 concentrations were observed in MHS-treated co-cultures and pOB mono-cultures compared with controls, indicating paracrine effects associated with MHS-induced angiogenesis. MHS-stimulated co-cultures and OEC mono-cultures released higher levels of Ang-2 than untreated cultures. On the other hand MHS treatment of co-cultures did not result in a clear effect regarding osteogenesis. Nevertheless, real-time PCR demonstrated that MHS increased the expression of mitogen-activated protein kinase, interleukin-6, and bone morphogenetic protein 2, known as HSP-related molecules in angiogenic and osteogenic regulation pathways. In agreement with these observations, the expression of some selected HSPs also increased at both the mRNA and protein levels in MHS-treated co-cultures.
机译:大型骨缺损的修复和再生,包括功能性脉管系统的形成,对组织工程和再生医学而言是一项极富挑战性的任务。最近的研究表明,轻度热应激(MHS)可以刺激血管生成和骨化,这将提供通过相对简单的方式增强骨骼再生过程的选择。但是,尚不清楚MHS增强血管生成和成骨的机制,以及所治疗细胞的潜在风险。我们已经研究了人类生殖内皮细胞(OEC)和原代成骨细胞(pOB)的共培养系统中MHS对血管生成和成骨的直接影响,并评估了细胞毒性作用以及各种热休克蛋白(HSP)的水平)在这些条件下合成。在7-14天的时间里,每周两次暴露于MHS(41°C,1 observedh)的共培养物中,观察到微血管样结构的形成增强。如实时聚合酶链反应(PCR)所示,血管内皮生长因子(VEGF),血管生成素1(Ang-1),血管生成素2(Ang-2)和肿瘤坏死因子-α的表达升高-在MHS处理的共培养后24小时进行调节。在蛋白质水平上,与对照组相比,在经MHS处理的共培养物和pOB单培养物中观察到VEGF和Ang-1浓度显着升高,表明与MHS诱导的血管生成有关的旁分泌效应。 MHS刺激的共培养物和OEC单培养物释放的Ang-2水平高于未处理的培养物。另一方面,共培养的MHS处理对成骨没有明显效果。尽管如此,实时PCR证明MHS在血管生成和成骨调节途径中增加了促分裂原活化蛋白激酶,白介素6和骨形态发生蛋白2(称为HSP相关分子)的表达。与这些观察结果一致,在经MHS处理的共培养物中,某些选定的HSP的表达在mRNA和蛋白质水平上也均增加。

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