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早期内皮祖细胞/髓系血管生成细胞表面表达的MMP-2/9的血管生成作用

Angiogenic Role of MMP-2/9 Expressed on the Cell Surface of Early Endothelial Progenitor Cells/Myeloid Angiogenic Cells.

作者信息

Kanayasu-Toyoda Toshie, Tanaka Takeshi, Ishii-Watabe Akiko, Kitagawa Hiroko, Matsuyama Akifumi, Uchida Eriko, Yamaguchi Teruhide

机构信息

Division of Biological Chemistry and Biologicals, National Institute of Health Sciences, Kamiyoga 1-18-1, Setagayaku, Tokyo, Japan.

Nihon Pharmaceutical University, Komuro 10281, Inamachi, Kitaadachigun, Saitama, Japan.

出版信息

J Cell Physiol. 2015 Nov;230(11):2763-75. doi: 10.1002/jcp.25002.

DOI:10.1002/jcp.25002
PMID:25820539
Abstract

Since the introduction of angiogenic cell therapy using early endothelial progenitor cells (EPCs), myeloid angiogenic cells (MACs) have been expected to be useful in treating ischemic diseases. In order to elucidate the angiogenic properties of MACs/EPCs, we clarified the characteristics of MACs as compared to M2 macrophages (Mϕs). Comparison of the gene expression profiles of MACs and late EPCs revealed that MACs expressed greater amounts of metalloproteinase (MMP)-9. It should be noted that the profile of MMP-2/9 expression on the cell surface of MACs was similar to that of M2 Mϕs, and that cell surface MMP-2/9 might be an active form based on molecular size. In addition, the invasion of MACs was prohibited not only by MMP-2/9 inhibitor, but also by the hyaluronidase treatment that caused the down-regulation of MMP-9 on the cell surface of MACs and inhibited their invasion activity. These results indicate that cell surface MMP-2/9 plays an important role in the high invasion ability of MACs. The conditioned medium of both MACs and M2 Mϕs stimulated tube formation of endothelial cells in vitro. MACs caused an increase in vessel formation in in vivo models through the production of IL-8. We propose that the role of MACs with cell surfaces expressing MMP-2/9 is rapidly invading ischemic tissue.

摘要

自从采用早期内皮祖细胞(EPCs)进行血管生成细胞治疗以来,髓样血管生成细胞(MACs)被认为在治疗缺血性疾病方面可能具有应用价值。为了阐明MACs/EPCs的血管生成特性,我们对比了MACs与M2巨噬细胞(Mϕs)的特征。MACs和晚期EPCs基因表达谱的比较显示,MACs表达的金属蛋白酶(MMP)-9更多。值得注意的是,MACs细胞表面MMP-2/9的表达模式与M2 Mϕs相似基于分子大小,细胞表面MMP-2/9可能是活性形式。此外,MACs的侵袭不仅被MMP-2/9抑制剂所抑制,透明质酸酶处理导致MACs细胞表面MMP-9下调并抑制其侵袭活性也能抑制其侵袭行为。这些结果表明,细胞表面MMP-2/9在MACs的高侵袭能力中起重要作用。MACs和M2 Mϕs的条件培养基在体外均能刺激内皮细胞形成管腔。MACs通过产生白细胞介素-8在体内模型中促进血管生成。我们提出,细胞表面表达MMP-2/9的MACs的作用是迅速侵入缺血组织

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