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延长缺氧培养和胰蛋白酶消化可提高人脂肪组织来源干细胞的促血管生成潜能。

Prolonged hypoxic culture and trypsinization increase the pro-angiogenic potential of human adipose tissue-derived stem cells.

机构信息

Department of Pharmacology, Aarhus University, Aarhus, Denmark.

出版信息

Cytotherapy. 2011 Mar;13(3):318-28. doi: 10.3109/14653249.2010.506505. Epub 2010 Aug 26.

Abstract

BACKGROUND AIMS

Transplantation of mesenchymal stromal cells (MSC), including adipose tissue-derived stem cells (ASC), is a promising option in the treatment of vascular disease. Short-term hypoxic culture of MSC augments secretion of anti-apoptotic and angiogenic cytokines. We hypothesized that prolonged hypoxic (1% and 5% oxygen) culture and trypsinization would augment ASC expression of anti-apoptotic and angiogenic cytokines and increase the angiogenic potential of ASC-conditioned media.

METHODS

The effects of prolonged hypoxic culture on growth and pro-angiogenic properties were investigated using human ASC cultured at 1%, 5% and 21% oxygen. The effect of trypsinization on the expression of pro-angiogenic genes was also determined.

RESULTS

Trypsinization induced up-regulation of the vascular endothelial growth factor (VEGF) and insulin-like growth factor-1 (IGF-1) genes independent of oxygen concentration. The expression of VEGF and IGF-1 was up-regulated in ASC cultured at 1% oxygen for 13 days compared with 4 days. The VEGF concentration in ASC-conditioned media was higher after prolonged hypoxic culture compared with short-term culture, while the IGF-1 and chemokine (CXC motif) ligand 12 (CXCL12) concentrations were unchanged. The VEGF receptor blocker SU5416 abolished angiogenesis in a cultured rat aortic ring model. Media from cells exposed to hypoxia increased angiogenesis, an effect that was dependent on factors other than just the VEGF concentration in the added media.

CONCLUSIONS

Optimization of the angiogenic potential of stem cell-based therapy in the treatment of vascular disease is important. We have demonstrated that prolonged hypoxic culture and trypsinization augment the therapeutic angiogenic potential of ASC.

摘要

背景目的

间充质基质细胞(MSC)的移植,包括脂肪组织来源的干细胞(ASC),是治疗血管疾病的一种很有前途的选择。MSC 的短期低氧培养增强了抗细胞凋亡和血管生成细胞因子的分泌。我们假设,延长低氧(1%和 5%氧气)培养和胰蛋白酶消化会增强 ASC 抗细胞凋亡和血管生成细胞因子的表达,并增加 ASC 条件培养基的血管生成潜力。

方法

使用在 1%、5%和 21%氧气下培养的人 ASC,研究延长低氧培养对生长和促血管生成特性的影响。还确定了胰蛋白酶消化对促血管生成基因表达的影响。

结果

胰蛋白酶消化诱导血管内皮生长因子(VEGF)和胰岛素样生长因子-1(IGF-1)基因的上调独立于氧浓度。与 4 天相比,在 1%氧气中培养 13 天的 ASC 中 VEGF 和 IGF-1 的表达上调。与短期培养相比,延长低氧培养后的 ASC 条件培养基中的 VEGF 浓度更高,而 IGF-1 和趋化因子(CXC 基序)配体 12(CXCL12)浓度不变。VEGF 受体阻滞剂 SU5416 可消除培养大鼠主动脉环模型中的血管生成。暴露于缺氧的细胞的培养基增加了血管生成,这种作用不仅依赖于添加培养基中 VEGF 浓度等因素。

结论

优化基于干细胞的治疗在治疗血管疾病中的血管生成潜力很重要。我们已经证明,延长低氧培养和胰蛋白酶消化增强了 ASC 的治疗性血管生成潜力。

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