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接种于明胶基水凝胶上的内皮细胞和肿瘤细胞在电刺激下的血管生成潜力。

Angiogenic potential of endothelial and tumor cells seeded on gelatin-based hydrogels in response to electrical stimulations.

作者信息

Tzoneva Rumiana, Uzunova Veselina, Apostolova Sonia, Krüger-Genge Anne, Neffe Axel T, Jung Friedrich, Lendlein Andreas

机构信息

Institute of Biophysics and Biomedical Engineering, Bulgarian Academy of Sciences, Sofia, Bulgaria.

Institute of Biomaterial Science and Berlin-Brandenburg Centre for Regenerative Therapies (BCRT), Helmholtz Zentrum Geesthacht, Teltow, Germany.

出版信息

Clin Hemorheol Microcirc. 2016;64(4):941-949. doi: 10.3233/CH-168040.

Abstract

Angiogenesis is one of the key processes during development, wound healing and tumor formation. Prerequisite for its existence is the presence of endogenous electrical fields (EFs) generated by active ion transport across polarized epithelia and endothelia, and appearance of the transcellular potentials. During angiogenesis cellular factor as endothelial growth factor (VEGF), synthesis of adhesive proteins and membrane metalloproteinases (MMPs) govern the angiogenic response to different external stimuli as biomaterials interactions and/or exogenous EF. Gelatin-based hydrogels with elasticities comparable to human tissues have shown to influence cell behavior as well as cell attachment, protein synthesis, VEGF and MMP's production after the application of EF. Gelatin-based matrices with 3 (G10_LNCO3), 5 (G10_LNCO5), and 8 (G10_LNCO8) fold excess of isocyanate groups per mol of amine groups present in gelatin were used. Human umbilical endothelial cells (HUVEC) (Lonza Basel, Switzerland) and highly invasive breast cancer MDA-MB-231 cells (ATCC®HTB-26TM) were used. For an estimation of the amount of VEGF released from cells a commercially available VEGF ELISA (Thermo Fisher Scientific, Germany) kit was used. Fibronectin (FN) enzyme immunoassay (EIA) was used to analyze the secreted amount of FN by cells seeded on the materials. Secreted MMPs were analyzed by zymography. Gelatin-based hydrogels attracted HUVEC adhesion and diminished the adhesion of MDA-MB-231 cells. The applied direct current (DC) EF induced an almost 5-fold increase in VEGF production by HUVEC seeded on gelatin-based hydrogels, while in contrast, the applied EF decreased the production of VEGF by cancer cells. FN synthesis was elevated in HUVEC cells seeded on gelatin-based materials in comparison to FN synthesis by cancer cells. HUVEC seeded on gelatin hydrogels showed an expression mainly of MMP-2. The application of EF increased the production of MMP-2 in HUVEC seeded on gelatin materials. In contrast, for MDA-MB-231 the production of MMPs on gelatin materials was lower compared to control materials. With the application of EF the levels of MMP-9 decreased but MMP-2 expression raised significantly for gelatin materials. Overall, the results showed that studied gelatin materials suppressed attachment of cancerous cells, as well as suppressed their angiogenic potential revealed by decreased VEGF and MMP production. Thus, this study approved gelatin-based hydrogels with proper elasticity characteristics and different degradation behavior as useful matrices for use in vascular tissue regeneration or in restriction of tumor growth after tumor resection.

摘要

血管生成是发育、伤口愈合和肿瘤形成过程中的关键过程之一。其存在的前提是存在由跨极化上皮细胞和内皮细胞的主动离子转运产生的内源性电场(EFs)以及跨细胞电位的出现。在血管生成过程中,细胞因子如内皮生长因子(VEGF)、粘附蛋白和膜金属蛋白酶(MMPs)的合成控制着对不同外部刺激(如生物材料相互作用和/或外源性EF)的血管生成反应。具有与人组织相当弹性的明胶基水凝胶已显示在施加EF后会影响细胞行为以及细胞附着、蛋白质合成、VEGF和MMP的产生。使用了每摩尔明胶中存在的胺基团具有3倍(G10_LNCO3)、5倍(G10_LNCO5)和8倍(G10_LNCO8)异氰酸酯基团过量的明胶基基质。使用了人脐静脉内皮细胞(HUVEC)(瑞士巴塞尔龙沙公司)和高侵袭性乳腺癌MDA-MB-231细胞(ATCC®HTB-26TM)。为了估计从细胞中释放的VEGF量,使用了市售的VEGF ELISA(德国赛默飞世尔科技公司)试剂盒。使用纤连蛋白(FN)酶免疫测定(EIA)来分析接种在材料上的细胞分泌的FN量。通过酶谱法分析分泌的MMPs。明胶基水凝胶吸引HUVEC附着并减少MDA-MB-231细胞的附着。施加的直流(DC)EF使接种在明胶基水凝胶上的HUVEC产生的VEGF增加了近5倍,而相比之下,施加的EF降低了癌细胞产生的VEGF。与癌细胞合成FN相比,接种在明胶基材料上的HUVEC细胞中FN合成增加。接种在明胶水凝胶上的HUVEC主要表达MMP-2。EF的施加增加了接种在明胶材料上的HUVEC中MMP-2的产生。相比之下,对于MDA-MB-231,明胶材料上MMPs的产生低于对照材料。随着EF的施加,明胶材料上MMP-9的水平降低,但MMP-2的表达显著升高。总体而言,结果表明所研究的明胶材料抑制癌细胞的附着,并通过降低VEGF和MMP的产生抑制其血管生成潜力。因此,本研究证实具有适当弹性特征和不同降解行为的明胶基水凝胶是用于血管组织再生或肿瘤切除后限制肿瘤生长的有用基质。

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