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恶性胶质瘤通过分泌血管生成细胞因子来积极招募骨髓基质细胞。

Malignant gliomas actively recruit bone marrow stromal cells by secreting angiogenic cytokines.

作者信息

Birnbaum Tobias, Roider Julia, Schankin Christoph J, Padovan Claudio S, Schichor Christian, Goldbrunner Roland, Straube Andreas

机构信息

Department of Neurology, Ludwig-Maximilians-University, Klinikum Grosshadern, Marchioninistr. 15, 81377 Munich, Germany.

出版信息

J Neurooncol. 2007 Jul;83(3):241-7. doi: 10.1007/s11060-007-9332-4. Epub 2007 Feb 14.

Abstract

The transplantation of progenitor cells is a promising new approach for the treatment of gliomas. Marrow stromal cells (MSC) are possible candidates for such a cell-based therapy, since they are readily and autologously available and show an extensive tropism to gliomas in vitro and in vivo. However, the signals that guide the MSC are still poorly understood. In this study, we show that gliomas have the capacity to actively attract MSC by secreting a multitude of angiogenic cytokines. We demonstrate that interleukin-8 (IL-8), transforming growth factor-ss1 (TGF-ss1) and neurotrophin-3 (NT-3) contribute to this glioma-directed tropism of human MSC. Together with the finding that vascular endothelial growth factor (VEGF) is another MSC-attracting factor secreted by glioma cells, these data support the hypothesis that gliomas use their angiogenic pathways to recruit mesenchymal progenitor cells.

摘要

祖细胞移植是一种很有前景的治疗神经胶质瘤的新方法。骨髓基质细胞(MSC)是这种基于细胞治疗的潜在候选者,因为它们易于自体获取,并且在体外和体内对神经胶质瘤都表现出广泛的嗜性。然而,引导MSC的信号仍知之甚少。在本研究中,我们表明神经胶质瘤能够通过分泌多种血管生成细胞因子来主动吸引MSC。我们证明白细胞介素-8(IL-8)、转化生长因子-β1(TGF-β1)和神经营养因子-3(NT-3)促成了人类MSC对神经胶质瘤的这种嗜性。连同血管内皮生长因子(VEGF)是神经胶质瘤细胞分泌的另一种吸引MSC的因子这一发现,这些数据支持了神经胶质瘤利用其血管生成途径招募间充质祖细胞的假说。

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