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5-脂氧合酶通路调控分化中的小鼠胚胎干细胞中的血管生成。

The 5-lipoxygenase pathway regulates vasculogenesis in differentiating mouse embryonic stem cells.

机构信息

Cardiology Division, Clinic of Internal Medicine I, Friedrich Schiller University, Erlanger Allee 101, Jena D-07743, Germany.

出版信息

Cardiovasc Res. 2010 Apr 1;86(1):37-44. doi: 10.1093/cvr/cvp385. Epub 2009 Dec 4.

Abstract

AIMS

It is well established that leukotrienes (LTs), products of the 5-lipoxygenase (5-LO) pathway, participate in inflammatory tissue reactions and immune responses. In the present study, the impact of the 5-LO pathway on vasculogenesis of mouse embryonic stem (ES) cells was investigated.

METHODS AND RESULTS

Immunohistochemistry studies demonstrated that 5-LO(+) cells first appeared at day 6 of embryoid body (EB) formation from ES cells. 5-LO(+)/CD68(+) as well as 5-LO(+)/CD45(+) cells were prominent at day 10 of EB differentiation. Real-time PCR and western blot analysis revealed all constituents of the 5-LO pathway. High performance liquid chromatography analyses indicated the synthesis of LTB(4) and LTD(4) in conformity with induction of the 5-LO pathway. Furthermore, Flk-1(+)/CD105(+) cells displayed calcium- (Ca(2+)) transients in response to LTB(4), whereas CD11b(+) cells responded to LTD(4). Treatment of EBs with LTB(4) and LTD(4) resulted in phosphorylation of the mitogen-activated protein kinase ERK1/2. Pharmacological inhibition of the 5-LO pathway and stable shRNA targeting of 5-LO-activating protein decreased capillary cell areas positive for PECAM-1.

CONCLUSION

Our data demonstrate that the 5-LO pathway emerges early during ES cell differentiation into cells of the myeloid lineage and that LTs play an until now unrecognized role in vascular development of ES cells.

摘要

目的

众所周知,白三烯(LTs)是 5-脂氧合酶(5-LO)途径的产物,参与炎症组织反应和免疫反应。在本研究中,研究了 5-LO 途径对小鼠胚胎干细胞(ES)血管生成的影响。

方法和结果

免疫组织化学研究表明,5-LO(+)细胞最早出现在 ES 细胞形成胚状体(EB)的第 6 天。5-LO(+)/CD68(+)和 5-LO(+)/CD45(+)细胞在 EB 分化的第 10 天明显增加。实时 PCR 和 Western blot 分析显示 5-LO 途径的所有组成部分。高效液相色谱分析表明 LTB(4)和 LTD(4)的合成与 5-LO 途径的诱导一致。此外,Flk-1(+)/CD105(+)细胞对 LTB(4)表现出钙(Ca(2+))瞬变,而 CD11b(+)细胞对 LTD(4)有反应。用 LTB(4)和 LTD(4)处理 EB 导致丝裂原活化蛋白激酶 ERK1/2 的磷酸化。5-LO 途径的药理学抑制和 5-LO 激活蛋白的稳定 shRNA 靶向减少了对 PECAM-1 呈阳性的毛细血管细胞面积。

结论

我们的数据表明,5-LO 途径在 ES 细胞分化为髓系细胞的早期出现,LTs 在 ES 细胞血管发育中发挥了迄今为止未被认识的作用。

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