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Human marrow-isolated adult multilineage-inducible (MIAMI) cells protect against peripheral vascular ischemia in a mouse model

机译:人类骨髓分离的成年多谱系诱导(MIAMI)细胞可在小鼠模型中预防周围血管缺血

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Background aims. The treatment of peripheral vascular disease (PVD) with stem cells potentially offers a promising strategy. We tested marrow-isolated adult multilineage-inducible (MIAMI) cells to induce neovascularization in a mouse model of critical hindlimb ischemia (CLI). Methods. CLI was induced in the right hindlimb of Balb/C mice. One million MIAMI cells, normally grown at 3% O2, were injected in the adductor muscle along the ischemic region. All animals (n 11 per group) were immunosuppressed with cyclosporine daily for the entire period. Human foreskin fibroblast (HFF) cells and phosphate-buffered saline (PBS) were used as controls. Blood perfusion in the ischemic right and non-ischemic left hindlimbs was measured. Results. Compared with animals receiving HFF cells or PBS, MIAMI cells significantly improved blood perfusion, necrosis and inflammation in the ischemic limb. A fraction of injected MIAMI cells expressed CD31 and von Willebrand factor (vWF). MIAMI cells in vitro, under pro-angiogenic growth conditions, differentiated into endothelial-like cells and expressed endothelial markers such as CD31 and vWF, determined by quantitative reverse transcriptasepolymerase chain reaction (qRT-PCR), and CD31 and kinase insert domain receptor (KDR), determined by immunofluorescence. Moreover, MIAMI cells formed vascular endothelial-like tubules in the presence of matrigel. Bioplex immunoassay analysis showed increased secretion of angiogenic/anti-inflammatory factors by the MIAMI cells under 3% O2 compared with 21% O2, including monocyte chemoattractant protein-1 (MCP-1), fractalkine (Ftk), growth-related oncogene (GRO), vascular endothelial growth factor (VEGF), interleukin (IL)-6 and IL-8. Furthermore, transcripts for anti-inflammatory molecules stanniocalcin-1 (STC-1) and tumor necrosis factor-α-stimulated gene 6 (TSG-6) were up-regulated several fold. Conclusions. MIAMI cells can be very useful for patients affected by CLI. MIAMI cells promote blood vessel formation and reduce inflammation and necrosis in ischemic tissue.
机译:背景目标。用干细胞治疗周围血管疾病(PVD)可能提供一种有前途的策略。我们在严重后肢缺血(CLI)小鼠模型中测试了骨髓分离的成人多谱系诱导(MIAMI)细胞诱导新血管形成。方法。在Balb / C小鼠的右后肢中诱导出CLI。一百万个通常以3%的O2浓度生长的MIAMI细胞沿着缺血区域注入内收肌中。在整个时期内,每天用环孢霉素免疫抑制所有动物(每组n 11)。使用人包皮成纤维细胞(HFF)和磷酸盐缓冲盐水(PBS)作为对照。测量了缺血性右后肢和非缺血性左后肢的血液灌注。结果。与接受HFF细胞或PBS的动物相比,MIAMI细胞显着改善了缺血肢体的血液灌注,坏死和炎症。一部分注入的MIAMI细胞表达CD31和von Willebrand因子(vWF)。体外MIAMI细胞在促血管生成生长条件下分化为内皮样细胞并表达内皮标记物,例如CD31和vWF,通过定量逆转录聚合酶链反应(qRT-PCR)以及CD31和激酶插入域受体(KDR)进行测定),通过免疫荧光测定。此外,在存在基质胶的情况下,MIAMI细胞形成了血管内皮样小管。生物复合体免疫分析表明,MIAMI细胞在3%氧气下的分泌增加了血管生成/抗炎因子,而21%的氧气包括单核细胞趋化蛋白1(MCP-1),分链烷烃(Ftk),生长相关癌基因(GRO) ),血管内皮生长因子(VEGF),白介素(IL)-6和IL-8。此外,抗炎分子staniocalcin-1(STC-1)和肿瘤坏死因子-α刺激的基因6(TSG-6)的转录本上调了几倍。结论MIAMI细胞对于受CLI影响的患者非常有用。 MIAMI细胞促进血管形成并减少缺血组织的炎症和坏死。

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