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血管内皮生长因子(VEGF)在正常条件下及肿瘤生长情况下小鼠胸腺中的作用

Role of Vascular Endothelial Growth Factor (VEGF) in Thymus of Mice under Normal Conditions and with Tumor Growth.

作者信息

Kisseleva E P, Krylov A V, Lyamina I V, Kudryavtsev I V, Lioudyno V I

机构信息

Institute for Experimental Medicine, St. Petersburg, 197376, Russia.

出版信息

Biochemistry (Mosc). 2016 May;81(5):491-501. doi: 10.1134/S0006297916050060.

Abstract

In our study, we for the first time investigated a role for VEGF as a factor regulating transendothelial migration of murine thymocytes in vitro. Effects of VEGF were examined in a model of thymocyte migration across a monolayer of EA.hy 926 endothelial cells. We showed that VEGF enhanced transendothelial migration of murine thymocytes and their adhesion to endothelial cells in a dose-dependent manner. VEGF did not influence thymocytes, but rather acted on endothelial cells by upregulating surface expression of adhesion molecule ICAM-1 and downregulating activity of 5'-nucleotidase. Effects from VEGF were comparable with those from TNF-α. Because it is known that administration of VEGF to intact animals results in thymic atrophy, it was assumed that it might play a role in developing thymic involution during tumor growth. Enhanced egress of thymocytes to the periphery was considered as a plausible mechanism underlying effects of VEGF. However, we revealed no difference in parameters of in vitro transendothelial migration for thymocytes from animals bearing a transplantable hepatoma 22a compared to control animals. VEGF mRNA expression in lysates of thymic stroma was found to be upregulated in mice with grafted tumors, whereas at the protein level the amount of VEGF did not differ. While examining expression of VEGF receptors on thymocytes by flow cytometry, both VEGFR-1 and VEGFR-2 were not detected, whereas the percentage of Nrp-1-positive thymocytes in animals with hepatoma 22a was as high as in the control group. Thus, we were unable to confirm a hypothesis regarding participation of VEGF in developing thymic involution during progression of experimental hepatoma. However, a set of novel data concerning a role for VEGF in stimulating transendothelial migration of thymocytes in vitro was obtained, and it may be of significance for understanding mechanisms underlying thymus functioning as well as a role of this cytokine in preparing endothelial cells for egress of thymocytes to the periphery.

摘要

在我们的研究中,我们首次研究了血管内皮生长因子(VEGF)作为体外调节小鼠胸腺细胞跨内皮迁移的一个因子的作用。在胸腺细胞穿过EA.hy 926内皮细胞单层的迁移模型中检测了VEGF的作用。我们发现,VEGF以剂量依赖的方式增强了小鼠胸腺细胞的跨内皮迁移及其与内皮细胞的黏附。VEGF并不影响胸腺细胞,而是通过上调黏附分子细胞间黏附分子-1(ICAM-1)的表面表达和下调5'-核苷酸酶的活性作用于内皮细胞。VEGF的作用与肿瘤坏死因子-α(TNF-α)的作用相当。由于已知向完整动物体内注射VEGF会导致胸腺萎缩,因此推测它可能在肿瘤生长过程中胸腺退化的发生中起作用。胸腺细胞向外周的流出增加被认为是VEGF作用的一个合理机制。然而,我们发现,与对照动物相比,携带可移植肝癌22a的动物的胸腺细胞体外跨内皮迁移参数没有差异。发现在移植肿瘤的小鼠中,胸腺基质裂解物中VEGF mRNA表达上调,而在蛋白质水平上,VEGF的量没有差异。在用流式细胞术检测胸腺细胞上VEGF受体的表达时,未检测到血管内皮生长因子受体-1(VEGFR-1)和血管内皮生长因子受体-2(VEGFR-2),而在患有肝癌22a的动物中,神经纤毛蛋白-1(Nrp-1)阳性胸腺细胞的百分比与对照组一样高。因此,我们无法证实关于VEGF参与实验性肝癌进展过程中胸腺退化的假说。然而,获得了一组关于VEGF在体外刺激胸腺细胞跨内皮迁移中作用的新数据,这对于理解胸腺功能的潜在机制以及这种细胞因子在使内皮细胞为胸腺细胞向外周流出做准备中的作用可能具有重要意义。

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